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JUNG, GYOO YEOL (정규열)
Dept. of Chemical Engineering(화학공학과)
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CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALLY EXPRESSED GENES:1||SWITCH:1||CONFORMATION POLYMORPHISM ANALYSIS:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide) triblock copolymer:1||Translation efficiency:1||PROTEIN EXPRESSION:1||FRACTIONATION:1||MEDIATED GENEREGULATION:1||EMERGING APPLICATIONS:1||APTAMERS:1||Enzymes:1||Substrates:1||Food safety:1||yl]phenol:1||point of care testing:1||isolation and purification:1||staphylococcal food poisoning:1||time factor:1||Bisbenzimidazole:1||Electrochemical Techniques:1||Foodborne Diseases:1||Humans:1||PointofCare Testing:1||Time Factors:1||MOLECULAR INVERSION PROBES:1||INTEGRATION:1||ALCOHOLS:1||Pseudomonas denitrificans:1||1,3Propanediol:1||Coenzyme B12:1||DIMETHYLBENZIMIDAZOLE:1||AQUEOUSSOLUTIONS:1||TOXICITY:1||FATTYACIDS:1||REGION:1||PEOPPOPEO triblock copolymer:1||Stufferfree MLPA:1||synthetic regulatory tools:1||RNA SECONDARY STRUCTURE:1||RHODOBACTERSPHAEROIDES:1||foodborne pathogen:1||Nucleicacidbased technology:1||Protein separation:1||TANDEMREPEAT ANALYSIS:1||secondary structure:1||DEFENSIN:1||autism spectrum disorder:1||copy number variation:1||CHROMOSOMAL REARRANGEMENTS:1||ABNORMALITIES:1||8P23.1:1||Y19:1||Bacillus psychrosaccharolyticus:1||pyruvate carboxylase:1||BACTERIAL ARTIFICIAL CHROMOSOMES:1||REPLICATION:1||AUrich sequence:1||untranslated region:1||COMBINATORIAL:1||RECOMBINANT ESCHERICHIACOLI:1||GLYCEROL METABOLISM:1||enzyme engineering:1||Electrophoresis:1||electrochemical analysis:1||human:1||procedures:1||LabOnAChip Devices:1||Salmonella enteritidis:1||Diagnostic methods:1||SOLUTION CONJUGATE ELECTROPHORESIS:1||Quantitative bioassay:1||MYCOBACTERIUMTUBERCULOSIS:1||Capillary electrophoresissingle strand conformation polymorphism:1||butyrate:1||Redox rebalancing:1||FORMATE DEHYDROGENASE:1||BLOCKCOPOLYMER:1||MODELS:1||COMMUNITY:1||PROMOTER LIBRARY:1||FLUX ANALYSIS:1||CHLAMYDOMONASREINHARDTII:1||SUSCEPTIBILITY:1||capillary electrophoresisbased singlestrand conformation polymorphism (CESSCP):1||multiplex polymerase chain reaction (PCR):1||LOCUS VARIABLENUMBER:1||FIELD GELELECTROPHORESIS:1||MICROFLUIDIC GENETICANALYSIS:1||SPECTRUM DISORDERS:1||Citrobacter sp:1||SUBTILIS:1||hydrogen production:1||Citrobacter sp Y19:1||WATER:1||DISEASE:1||CHALLENGES:1||RIBOSOMEMESSENGER RECOGNITION:1||BINDING:1||COPOLYMER:1||MEDIA:1||PROMOTERS:1||MICROCHANNELS:1||SYSTEMS:1||SELECTION:1||CHAIN LENGTH:1||COENZYME:1||STEP:1||Evolutionary approach:1||hydracrylic acid:1||catalysis:1||molecular evolution:1||Chains:1||Chemical detection:1||Voltammetry:1||ELectrochemical detection:1||film based integrated chip:1||process optimization:1||Nucleic Acid Amplification Techniques:1||Diagnostic assay:1||Ligasebased genotyping assay:1||Hexanoic acid:1||AtoB:1||1BUTANOL:1||ETHANOL:1||GLYCEROL:1||1,3PROPANEDIOL:1||BLOCKCOPOLYMER SURFACTANTS:1||heterologous pathway:1||METABOLIC BURDEN:1||PYRUVATEDEHYDROGENASE COMPLEX:1||Polymer blend:1||FOODBORNE PATHOGENS:1||cellular phenotype:1||dynamic control:1||essential gene:1||Swine H1N1 influenza:1||E. COLI:1||Photofermentation:1||Biophotolysis:1||ARRAY ELECTROPHORESIS:1||Foodborne pathogens:1||CAPILLARYZONEELECTROPHORESIS:1||psychrophilicity:1||Corynebacterium glutamicum:1||aspartate kinase:1||LLYSINE:1||Red system:1||PEPTIDES:1||RNA SECONDARY STRUCTURES:1||PARTICLE:1||FLOW:1||FLAVONOIDS:1||HEMEBIOSYNTHESIS:1||Aldehyde dehydrogenase:1||Catalytic efficiencies:1||Directed evolution:1||enzyme inactivation:1||enzyme substrate:1||Microfluidics:1||DNA analysis:1||Electrochemical signals:1||Microfluidic chambers:1||controlled study:1||genetic procedures:1||microorganism detection:1||quantitative analysis:1||lab on a chip:1||nucleic acid amplification:1||CESSCP:17||IDENTIFICATION:11||CE:11||CAPILLARYELECTROPHORESIS:10||EXPRESSION:10||SSCP:10||SEPARATION:10||PCR:9||REALTIME PCR:8||POLYMERASECHAINREACTION:8||ASSAY:8||STRAND CONFORMATION POLYMORPHISM:6||SYSTEM:6||RESOLUTION CESSCP:6||ESCHERICHIACOLI:6||Pathogen detection:5||MLPA:5||GROWTH:5||DNA MICROARRAY:5||DNA:5||BIOSYNTHESIS:5||GENES:5||metabolic engineering:5||Pathogen:4||ESCHERICHIACOLI O157H7:4||BACTERIA:4||DEPENDENT PROBE AMPLIFICATION:4||Polymer matrix:4||Escherichia coli:4||Diagnosis:4||RIBOSOMALRNA GENE:4||PROTEINS:4||SYNTHETIC BIOLOGY:3||OPTIMIZATION:3||DIAGNOSTICS:3||Staphylococcus aureus:3||MUTATIONS:3||Synthetic biology:3||STAPHYLOCOCCUSAUREUS:3||MESSENGERRNA:3||BACTERIAL PATHOGENS:3||High resolution:3||RTPCR:3||PROTEIN:3||GLUCOSE:3||MICROBIAL COMMUNITY:3||RIBOSOMALRNA:3||16S rRNA gene:3||RNA:3||Stufferfree multiplex ligationdependent probe amplification:3||QUANTIFICATION:3||CO:3||STRAINS:3||Metabolic engineering:3||Capillary electrophoresissinglestrand conformation polymorphism:3||LISTERIAMONOCYTOGENES:3||GENE:3||AMPLIFICATION:3||H2:3||INITIATION:3||isolation:2||watergas shift reaction:2||5 &apos:2||IRON CATALYST:2||Highresolution:2||FOOD:2||biohydrogen:2||pentose phosphate pathway:2||METABOLICFLUX ANALYSIS:2||Bacterial consortium:2||PAHS:2||GENEEXPRESSION:2||TRANSLATION:2||MICROFLUIDICS:2||IMPEDANCE BIOSENSOR:2||SENSOR:2||Pluronic polymer:2||GELELECTROPHORESIS:2||SALMONELLATYPHIMURIUM:2||synthetic biology:2||VARIANTS:2||LASERINDUCED FLUORESCENCE:2||SAMPLES:2||PATHOGENS:2||ELECTRONICSTRUCTURE:2||DESIGN:2||foodborne pathogens:2||RNA quantification:2||Common primer:2||Templatetagging:2||BIOREMEDIATION:2||CODEHYDROGENASE:2||KINASE INHIBITORS:2||MATRIX:2||3Hydroxypropionic acid:2||MICROBIALPRODUCTION:2||SELECTIVE SYNTHESIS:2||NANOPARTICLES:2||DENSITY:2||Copy number variation:2||BIOHYDROGEN PRODUCTION:2||multiplex analysis:2||FOODBORNE PATHOGENS:2||Enhanced biodegradation:2||SOILSLURRY SYSTEMS:2||SEQUENCE:2||priority journal:2||MULTIPLE PATHOGENS:2||TRIBLOCK COPOLYMER:2||Multiplex ligationdependent probe amplification:2||GLUTARALDEHYDE:2||DUAL GENETIC SELECTION:2||OIL:2||Article:2||food poisoning:2||SENSITIVE DETECTION:2||Multiplex analysis:2||METABOLISM:2||PATHOGEN DETECTION:2||CHIRALITY:2||RAPID DETECTION:2||SALMONELLA:2||GENOME:2||MATURATION:2||template tagging:2||MULTIPLEX PCR:2||PAH:2||MANGROVE SEDIMENTS:2||BIODEGRADATION:2||PATHWAY:2||nonhuman:2||FOOD SAMPLES:2||MICROCHIP ELECTROPHORESIS:2||FERMENTATION:2||ACID:2||Multiplex detection:2||E. coli:2||OPERON:2||VALIDATION:2||POLYCYCLIC AROMATICHYDROCARBONS:2||CELLSURFACE HYDROPHOBICITY:2||COMPLEX:2||Antibodyconjugated magnetic nanoparticles:2||YEAST:2||CLOSTRIDIUMTYROBUTYRICUM:2||NAD(P)Hdependent hydrogen production:2||BIOSURFACTANT:2||Genetic polymorphisms:1||MUTATION DETECTION:1||Spinal muscular atrophy:1||CHINESE:1||SMN1:1||nbutanol:1||LIQUIDCRYSTALS:1||GELATION:1||Stuffer sequence:1||Foodborne pathogen:1||Microchip:1||TRANSLATIONAL EFFICIENCY:1||ESCHERICHIACOLI STRAINS:1||HYPERTHERMOPHILIC ARCHAEON:1||ENTEROBACTERAEROGENES:1||RESOLUTION:1||PRIMING OLIGONUCLEOTIDE SYSTEM:1||translational efficiency:1||5&apos:1||stabilization:1||mRNA:1||ENZYMES:1||ADAPTATION:1||lagging strand:1||PHAGELAMBDA:1||tunable expression:1||QUANTITATIVE RTPCR:1||CODON:1||BLOOD:1||PHOSPHOENOLPYRUVATE:1||Glycerol:1||Biological production:1||enrichment culture:1||Polymerase chain reaction:1||double stranded DNA:1||colony forming unit:1||gene amplification:1||measurement accuracy:1||reproducibility:1||square wave voltammetry:1||microbiology:1||Ligasebased genotyping:1||TECHNOLOGY:1||DIAGNOSIS:1||MCT1:1||Quantitative analysis:1||VIRUS:1||REARRANGEMENTS:1||Antibiotic susceptibility test:1||Highresolution CESSCP:1||HETEROLOGOUS BIOSYNTHESIS:1||THERMOCOCCUSKODAKARAENSIS:1||Maximum doubling cycle:1||quantitative correlation:1||UNTRANSLATED REGION:1||REGIONS:1||ETIOLOGY:1||GLYCOLYSIS:1||PYRUVATECARBOXYLASE:1||ASPARTOKINASE:1||Capillary electrophoresis singlestrand conformation polymorphism:1||Multiplex polymerase chain reaction:1||BACILLUSCEREUS:1||annealing:1||recombination:1||BACTERIOPHAGELAMBDA:1||antimicrobial agent:1||UTR:1||expression analysis:1||COMMUNITIES:1||MICROSPHERES:1||Binding sites:1||binding site:1||Gene expression:1||Square wave voltammetry:1||Food microbiology:1||polycarbonate:1||polyester:1||polyimide:1||genetics:1||Salmonella enterica serovar Enteritidis:1||Salmonella food poisoning:1||ROLLING CIRCLE AMPLIFICATION:1||COPY NUMBER VARIATION:1||SNP:1||TIME:1||Kluyveromyces marxianus:1||Singlenucleotide polymorphism:1||PREDICTION:1||SMA:1||BIOSYNTHETIC GENES:1||SHERMANII:1||LIGAND:1||synthetic scaffold:1||K12:1||POLYMER:1||SACCHAROMYCESCEREVISIAE:1||THERAPY:1||QUANTITATIVEANALYSIS:1||Cell separation:1||16S RIBOSOMALRNA:1||Quantification:1||Poly(ethyleneoxide)poly(propyleneoxide)poly(ethyleneoxide):1||BLOCKCOPOLYMERS:1||stability:1||downstream region:1||RIBOSOME BINDING:1||VIBRIOPARAHAEMOLYTICUS:1||CAMPYLOBACTERJEJUNI:1||arraycomparative genomic hybridization:1||LINKAGE DISEQUILIBRIUM:1||POLYMORPHISMS:1||CARBONMONOXIDE:1||Rhodopseudomonas palustris:1||twodimensional gel electrophoresis:1||GENERAL STRESSRESPONSE:1||COLD:1||lysine:1||amino acid fermentation:1||replication:1||BETAPROTEIN:1||expressional PCR:1||SD sequence:1||TRANSCRIPTS:1||mRNA quantification:1||MAGNETIC NANOPARTICLES:1||BIOTECHNOLOGICAL PRODUCTION:1||BIOSENSORS:1||TRANSCRIPTION:1||DELTAAMINOLEVULINICACID:1||ITACONIC ACID:1||HIGHYIELD:1||Aldehydes:1||Metabolism:1||Transcription:1||Transcription factors:1||aldehyde dehydrogenase:1||aldehyde derivative:1||molecular library:1||Pathogens:1||High reproducibility:1||Pointofcare testing:1||4 [5 (4 methyl 1 piperazinyl)[2,5&apos:1||bi 1h benzimidazol] 2&apos:1||pibenzimol:1||electrochemical detection:1||potentiometry:1||chemistry:1||Reproducibility of Results:1||Salmonella Food Poisoning:1||Staphylococcal Food Poisoning:1||SENSITIVE CAPILLARYELECTROPHORESIS:1||TES1:1||SUGAR:1||POLYMORPHISM:1||COBALAMIN VITAMINB12:1||Respiratory tract infection:1||Foodborne pathogen detection:1||INFECTIONS:1||BACTEREMIA:1||expression control:1||Biohydrogen:1||ALPHADEFENSIN:1||GENETICS:1||wheat germ:1||RHODOSPIRILLUMRUBRUM:1||Infectious disease:1||BREAK REPAIR:1||COMBINATORIAL CHEMISTRY:1||DRUG DISCOVERY:1||PROTEIN S1:1||mRNA secondary structure:1||SECONDARY STRUCTURE:1||RIBOSOME:1||CIRCULATING TUMORCELLS:1||AMINOACIDS:1||BIOSYNTHETIC PATHWAYS:1||EVOLUTION:1||KLEBSIELLAPNEUMONIAE:1||COMBINATORIAL DESIGN:1||CAENORHABDITISELEGANS:1||Screening:1||Semialdehyde dehydrogenase:1||gel electrophoresis:1||microfluidics:1||polymerase chain reaction:1||Biosensing Techniques:1||CHAINREACTION:1||DNALIGASE:1||GALACTITOL:1||Halogenation:1||Ambient temperature:1||Metabolic imbalance:1||MICELLIZATION:1||Pathogenspecific gene:1||PROTOCOL:1||simultaneous detection:1||Dark fermentation:1||ENHANCED HYDROGENPRODUCTION:1||H2 PRODUCTION:1||PCR PRIMER DESIGN:1||Multiplex PCRCE analysis:1||Microdevice:1||cellfree protein synthesis system:1||proteome:1||LOWTEMPERATURE:1||ARCHAEA:1||TREHALOSE:1||CARBONMONOXIDE DEHYDROGENASE:1||OVERPRODUCTION:1||CYTOTOXIN:1||HOMOLOGOUS RECOMBINATION:1||microbial community:1||antimicrobial activity analysis:1||STRANDCONFORMATION POLYMORPHISM:1||BACTERIAL:1||ELECTROPHORESIS:1||SEQUENCES:1||SITES:1||enhanced green fluorescent protein:1||DIFFERENTIALL
