| scholarly article | Q13442814 |
| P2093 | author name string | B L Wanner | |
| A Haldimann | |||
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| Construction of new beta-glucuronidase cassettes for making transcriptional fusions and their use with new methods for allele replacement | Q72841100 | ||
| P433 | issue | 21 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | bacteria | Q10876 |
| P304 | page(s) | 6384-6393 | |
| P577 | publication date | 2001-11-01 | |
| P1433 | published in | Journal of Bacteriology | Q478419 |
| P1476 | title | Conditional-replication, integration, excision, and retrieval plasmid-host systems for gene structure-function studies of bacteria | |
| P478 | volume | 183 |
| Q40031715 | A BTP1 prophage gene present in invasive non-typhoidal Salmonella determines composition and length of the O-antigen of the lipopolysaccharide |
| Q38409720 | A BioBrick™-Compatible Vector for Allelic Replacement Using the XylE Gene as Selection Marker |
| Q34547514 | A Multiplexed Single-Cell CRISPR Screening Platform Enables Systematic Dissection of the Unfolded Protein Response |
| Q90253583 | A PopZ-linked apical recruitment assay for studying protein-protein interactions in the bacterial cell envelope |
| Q34395186 | A bidirectional fluorescent two-hybrid system for monitoring protein-protein interactions |
| Q54515474 | A comparative study of variation in codon 33 of the rpoS gene in Escherichia coli K12 stocks: implications for the synthesis of σs |
| Q50521602 | A convenient method for multiple insertions of desired genes into target loci on the Escherichia coli chromosome. |
| Q35192443 | A fail-safe mechanism in the septal ring assembly pathway generated by the sequential recruitment of cell separation amidases and their activators |
| Q24682421 | A natural genetic code expansion cassette enables transmissible biosynthesis and genetic encoding of pyrrolysine |
| Q49851989 | A network of regulators promotes dehydration tolerance in Escherichia coli. |
| Q34330387 | A new activity for an old enzyme: Escherichia coli bacterial alkaline phosphatase is a phosphite-dependent hydrogenase |
| Q42535677 | A new glimpse of FadR-DNA crosstalk revealed by deep dissection of the E. coli FadR regulatory protein |
| Q35433183 | A new regulatory mechanism for bacterial lipoic acid synthesis. |
| Q34237888 | A nutrient-tunable bistable switch controls motility in Salmonella enterica serovar Typhimurium. |
| Q27649896 | A peptide deformylase-ribosome complex reveals mechanism of nascent chain processing |
| Q34518644 | A place for everything: chromosomal integration of large constructs |
| Q28817594 | A population-based temporal logic gate for timing and recording chemical events |
| Q35546037 | A predicted ABC transporter, FtsEX, is needed for cell division in Escherichia coli |
| Q35311391 | A rapid and reliable strategy for chromosomal integration of gene(s) with multiple copies |
| Q35885858 | A set of powerful negative selection systems for unmodified Enterobacteriaceae |
| Q40980796 | A standard vector for the chromosomal integration and characterization of BioBrick™ parts in Escherichia coli |
| Q35683452 | A strategy for enhanced circular DNA construction efficiency based on DNA cyclization after microbial transformation |
| Q35800309 | A strategy of gene overexpression based on tandem repetitive promoters in Escherichia coli |
| Q46366557 | A synthetic gene-metabolic oscillator. |
| Q33422974 | A toxin-antitoxin system promotes the maintenance of an integrative conjugative element |
| Q40897496 | A versatile element for gene addition in bacterial chromosomes |
| Q34946239 | A whole-cell biosensor for the detection of gold |
| Q37232478 | ATP-binding site lesions in FtsE impair cell division. |
| Q54384011 | Activation of the AtoSC two-component system in the absence of the AtoC N-terminal receiver domain in E. coli. |
| Q33582122 | Alternative sigma factor sigmaH modulates prophage integration and excision in Staphylococcus aureus |
| Q36704156 | Amino acids important for DNA recognition by the response regulator OmpR. |
| Q40101578 | Amplifying genetic logic gates |
| Q35546844 | An ATP-binding cassette transporter-like complex governs cell-wall hydrolysis at the bacterial cytokinetic ring. |
| Q35762450 | An Integrated System for Precise Genome Modification in Escherichia coli |
| Q42042348 | Anaerobic obligatory xylitol production in Escherichia coli strains devoid of native fermentation pathways |
| Q45165817 | Analysis of the role of intraprotein electron transfer in photoreactivation by DNA photolyase in vivo |
| Q37264341 | Antagonistic control of the turnover pathway for the global regulatory sRNA CsrB by the CsrA and CsrD proteins. |
| Q64076506 | Application of leucine dehydrogenase Bcd from for l-valine synthesis in under microaerobic conditions |
| Q37893526 | Application of the bacteriophage Mu-driven system for the integration/amplification of target genes in the chromosomes of engineered Gram-negative bacteria--mini review |
| Q54201986 | Asymmetric polar localization dynamics of the serine chemoreceptor protein Tsr in Escherichia coli. |
| Q24614165 | Bacterial actin MreB assembles in complex with cell shape protein RodZ. |
| Q34160920 | Bacterial sugar utilization gives rise to distinct single-cell behaviours |
| Q38179994 | Bacteriophage recombination systems and biotechnical applications. |
| Q33657298 | BglBricks: A flexible standard for biological part assembly |
| Q48251407 | Biased partitioning of the multidrug efflux pump AcrAB-TolC underlies long-lived phenotypic heterogeneity |
| Q40862607 | Binding of Shewanella FadR to the fabA fatty acid biosynthetic gene: implications for contraction of the fad regulon |
| Q47131320 | Biosensor-aided high-throughput screening of hyper-producing cells for malonyl-CoA-derived products. |
| Q61807409 | Biosensor-guided improvements in salicylate production by recombinant Escherichia coli |
| Q91671413 | CRIMoClo plasmids for modular assembly and orthogonal chromosomal integration of synthetic circuits in Escherichia coli |
| Q38290237 | Cadmium toxicity in glutathione mutants of Escherichia coli |
| Q37065875 | Cell death from antibiotics without the involvement of reactive oxygen species |
| Q42125850 | CfaD-dependent expression of a novel extracytoplasmic protein from enterotoxigenic Escherichia coli. |
| Q39897568 | Characterization of a mannose utilization system in Bacillus subtilis |
| Q34247945 | Characterization of an inducible promoter in different DNA copy number conditions. |
| Q34760785 | Characterization of flavin-based fluorescent proteins: an emerging class of fluorescent reporters |
| Q34077717 | Characterization of the roles of the catalytic domains of Mycobacterium tuberculosis ligase D in Ku-dependent error-prone DNA end joining |
| Q34565389 | Chromosomal evolution of Escherichia coli for the efficient production of lycopene |
| Q33534627 | Ciprofloxacin causes persister formation by inducing the TisB toxin in Escherichia coli |
| Q41372447 | Circuitry Linking the Catabolite Repression and Csr Global Regulatory Systems of Escherichia coli. |
| Q35046553 | Circuitry linking the Csr and stringent response global regulatory systems |
| Q42777763 | Circuitry linking the global Csr and σE-dependent cell envelope stress response systems. |
| Q49025389 | Clonetegration Using OSIP Plasmids: One-Step DNA Assembly and Site-Specific Genomic Integration in Bacteria. |
| Q46353242 | Co-utilization of hexoses by a microconsortium of sugar-specific E. coli strains |
| Q33570169 | Common requirement for the relaxosome of plasmid R1 in multiple activities of the conjugative type IV secretion system |
| Q40222146 | Complete nucleotide sequence and annotation of the temperate corynephage ϕ16 genome. |
| Q38664185 | Complex chromosomal neighborhood effects determine the adaptive potential of a gene under selection. |
| Q35296562 | Complex regulation of the global regulatory gene csrA: CsrA-mediated translational repression, transcription from five promoters by Eσ⁷⁰ and Eσ(S), and indirect transcriptional activation by CsrA |
| Q35196256 | Compounds targeting disulfide bond forming enzyme DsbB of Gram-negative bacteria |
| Q37104508 | Conjugative DNA Transfer Is Enhanced by Plasmid R1 Partitioning Proteins |
| Q36517713 | Construction and characterization of an in-vivo linear covalently closed DNA vector production system. |
| Q22122301 | Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants: the Keio collection |
| Q48298401 | Construction of targeted single copy lac fusions using lambda Red and FLP-mediated site-specific recombination in bacteria |
| Q37596245 | Continuous control in bacterial regulatory circuits |
| Q50044494 | Continuous control of flagellar gene expression by the σ28-FlgM regulatory circuit in Salmonella enterica |
| Q33609856 | Creating Single-Copy Genetic Circuits |
| Q34222163 | Critical design criteria for minimal antibiotic‐free plasmid vectors necessary to combine robust RNA Pol II and Pol III‐mediated eukaryotic expression with high bacterial production yields |
| Q36012615 | Cro's role in the CI Cro bistable switch is critical for {lambda}'s transition from lysogeny to lytic development |
| Q36070050 | Cross Talk Inhibition Nullified by a Receiver Domain Missense Substitution |
| Q34431014 | Crosstalk of Escherichia coli FadR with global regulators in expression of fatty acid transport genes |
| Q34496912 | CsrA Participates in a PNPase Autoregulatory Mechanism by Selectively Repressing Translation of pnp Transcripts That Have Been Previously Processed by RNase III and PNPase |
| Q43208080 | CsrA activates flhDC expression by protecting flhDC mRNA from RNase E-mediated cleavage. |
| Q35530981 | CsrA represses translation of sdiA, which encodes the N-acylhomoserine-L-lactone receptor of Escherichia coli, by binding exclusively within the coding region of sdiA mRNA. |
| Q43192580 | Cyclic AMP receptor protein-dependent repression of heat-labile enterotoxin |
| Q36155174 | Cysteine catabolism and cysteine desulfhydrase (CdsH/STM0458) in Salmonella enterica serovar typhimurium |
| Q33845937 | Daughter cell separation is controlled by cytokinetic ring-activated cell wall hydrolysis |
| Q44885753 | Deciphering interactions used by the influenza virus NS1 protein to silence the host antiviral sensor protein RIG-I using a bacterial reverse two-hybrid system |
| Q35113909 | Design and application of a novel high-throughput screening technique for 1-deoxynojirimycin |
| Q36845531 | Determination of antibiotic hypersensitivity among 4,000 single-gene-knockout mutants of Escherichia coli |
| Q91594957 | Developing a highly efficient hydroxytyrosol whole-cell catalyst by de-bottlenecking rate-limiting steps |
| Q47104312 | Development of a high efficiency integration system and promoter library for rapid modification of Pseudomonas putida KT2440. |
| Q44708928 | Development of a novel method of lytic phage delivery by use of a bacteriophage P22 site-specific recombination system |
| Q41921895 | Development of pVCR94ΔX from Vibrio cholerae, a prototype for studying multidrug resistant IncA/C conjugative plasmids. |
| Q37156985 | Differences in hydrogenase gene expression between Methanosarcina acetivorans and Methanosarcina barkeri |
| Q35668053 | Dimerization of the bacterial biotin carboxylase subunit is required for acetyl coenzyme A carboxylase activity in vivo |
| Q33881285 | Direct and convenient measurement of plasmid stability in lab and clinical isolates of E. coli. |
| Q42243754 | Directed evolution of a thermostable phosphite dehydrogenase for NAD(P)H regeneration |
| Q38897833 | Directed evolution of λ integrase activity and specificity by genetic derepression |
| Q37732584 | Disassembly of the divisome in Escherichia coli: evidence that FtsZ dissociates before compartmentalization |
| Q33558045 | Discovery and characterization of three new Escherichia coli septal ring proteins that contain a SPOR domain: DamX, DedD, and RlpA |
| Q33928870 | DsbL and DsbI contribute to periplasmic disulfide bond formation in Salmonella enterica serovar Typhimurium |
| Q37008947 | Dual posttranscriptional regulation via a cofactor-responsive mRNA leader |
| Q30847197 | Dual-In/Out strategy for genes integration into bacterial chromosome: a novel approach to step-by-step construction of plasmid-less marker-less recombinant E. coli strains with predesigned genome structure. |
| Q49953352 | Dynamic Measures of Flagellar Gene Expression |
| Q91977913 | Dynamic control of toxic natural product biosynthesis by an artificial regulatory circuit |
| Q43473881 | Dynamic enzyme docking to the ribosome coordinates N-terminal processing with polypeptide folding. |
| Q35739192 | Dynamic subcellular localization of a respiratory complex controls bacterial respiration. |
| Q37533617 | Dynamics of the serine chemoreceptor in the Escherichia coli inner membrane: a high-speed single-molecule tracking study |
| Q54338814 | E. coli LoiP (YggG), a metalloprotease hydrolyzing Phe-Phe bonds. |
| Q53295264 | Effects of chromosomal gene copy number and locations on polyhydroxyalkanoate synthesis by Escherichia coli and Halomonas sp. |
| Q34317645 | Effects of the P1 plasmid centromere on expression of P1 partition genes |
| Q35074922 | Effects of the global regulator CsrA on the BarA/UvrY two-component signaling system |
| Q41880930 | Electrode-assisted acetoin production in a metabolically engineered Escherichia coli strain |
| Q89685405 | Engineered probiotics for local tumor delivery of checkpoint blockade nanobodies |
| Q46776849 | Engineering complex biological systems in bacteria through recombinase-assisted genome engineering |
| Q59260608 | Engineering orthogonal synthetic timer circuits based on extracytoplasmic function σ factors |
| Q84653141 | Enhanced co-production of hydrogen and poly-(R)-3-hydroxybutyrate by recombinant PHB producing E. coli over-expressing hydrogenase 3 and acetyl-CoA synthetase |
| Q53303322 | Enhanced production of poly-3-hydroxybutyrate by Escherichia coli over-expressing multiple copies of NAD kinase integrated in the host genome. |
| Q42248495 | Enterohemorrhagic Escherichia coli O157:H7 gal mutants are sensitive to bacteriophage P1 and defective in intestinal colonization |
| Q47837168 | Escherichia coli cytochrome c peroxidase is a respiratory oxidase that enables the use of hydrogen peroxide as a terminal electron acceptor |
| Q34414825 | Escherichia coli flagellar genes as target sites for integration and expression of genetic circuits. |
| Q37713153 | Escherichia coli isolate for studying colonization of the mouse intestine and its application to two-component signaling knockouts |
| Q24676980 | Escherichia coli phnN , Encoding Ribose 1,5-Bisphosphokinase Activity (Phosphoribosyl Diphosphate Forming): Dual Role in Phosphonate Degradation and NAD Biosynthesis Pathways |
| Q39607542 | Establishing and maintaining sequestration of Dam target sites for phase variation of agn43 in Escherichia coli. |
| Q43932960 | Evidence for function overlapping of CymA and the cytochrome bc1 complex in the Shewanella oneidensis nitrate and nitrite respiration |
| Q35034394 | Evolutionary tuning of protein expression levels of a positively autoregulated two-component system |
| Q36760543 | Exoprotein production correlates with morphotype changes of nonmotile Shewanella oneidensis mutants. |
| Q46893998 | Expanding the chemical diversity of natural esters by engineering a polyketide-derived pathway into Escherichia coli. |
| Q33855616 | Expression levels influence ribosomal frameshifting at the tandem rare arginine codons AGG_AGG and AGA_AGA in Escherichia coli |
| Q38300978 | Expression of Mycobacterium tuberculosis Ku and Ligase D in Escherichia coli results in RecA and RecB-independent DNA end-joining at regions of microhomology |
| Q33962924 | ExsA recruits RNA polymerase to an extended -10 promoter by contacting region 4.2 of sigma-70 |
| Q42125249 | FimA, FimF, and FimH are necessary for assembly of type 1 fimbriae on Salmonella enterica serovar Typhimurium |
| Q37336075 | FimY does not interfere with FimZ-FimW interaction during type 1 fimbria production by Salmonella enterica serovar Typhimurium |
| Q36747807 | FliZ Is a posttranslational activator of FlhD4C2-dependent flagellar gene expression |
| Q34465314 | Fluorescence correlation spectroscopy measurements of the membrane protein TetA in Escherichia coli suggest rapid diffusion at short length scales |
| Q28272542 | Function and regulation of isoforms of carbon monoxide dehydrogenase/acetyl coenzyme A synthase in Methanosarcina acetivorans |
| Q33635059 | Functional profiling of p53-binding sites in Hdm2 and Hdmx using a genetic selection system |
| Q34747040 | Functional roles for the GerE-family carboxyl-terminal domains of nitrate response regulators NarL and NarP of Escherichia coli K-12 |
| Q41911664 | Fur regulates expression of the Salmonella pathogenicity island 1 type III secretion system through HilD. |
| Q30376672 | Generic plasmid DNA production platform incorporating low metabolic burden seed-stock and fed-batch fermentation processes. |
| Q46314604 | Genetic analysis of the Salmonella transcription factor HilA. |
| Q34675381 | Genetic analysis of the cell division protein FtsI (PBP3): amino acid substitutions that impair septal localization of FtsI and recruitment of FtsN. |
| Q38037552 | Genetic manipulation of Staphylococci-breaking through the barrier. |
| Q35140832 | Genetic strategies for antibacterial drug discovery |
| Q34177935 | Genetics and Regulation of the Major Enzymes of Alanine Synthesis inEscherichia coli |
| Q41746387 | Genome-Wide Transcriptional Response to Varying RpoS Levels in Escherichia coli K-12 |
| Q36310375 | Global analysis of translation termination in E. coli. |
| Q33724452 | Global effects of the DEAD-box RNA helicase DeaD (CsdA) on gene expression over a broad range of temperatures |
| Q33432897 | Guidance for data collection and computational modelling of regulatory networks |
| Q49597228 | HilE Regulates HilD by Blocking DNA Binding in Salmonella enterica serovar Typhimurium |
| Q34789422 | Horizontally acquired glycosyltransferase operons drive salmonellae lipopolysaccharide diversity |
| Q37252991 | How Escherichia coli tolerates profuse hydrogen peroxide formation by a catabolic pathway |
| Q34637796 | Hydrogen peroxide inactivates the Escherichia coli Isc iron-sulphur assembly system, and OxyR induces the Suf system to compensate |
| Q92772472 | Identification of new components of the RipC-FtsEX cell separation pathway of Corynebacterineae |
| Q28486179 | Identification of the SlmA active site responsible for blocking bacterial cytokinetic ring assembly over the chromosome |
| Q33330047 | Identifying small-molecule modulators of protein-protein interactions |
| Q34045588 | Imaging OmpR binding to native chromosomal loci in Escherichia coli |
| Q44114736 | Implementation of stable and complex biological systems through recombinase-assisted genome engineering |
| Q53436924 | Improved NADPH supply for xylitol production by engineered Escherichia coli with glycolytic mutations. |
| Q37399763 | Improved antibiotic-free DNA vaccine vectors utilizing a novel RNA based plasmid selection system |
| Q36256811 | Improving key enzyme activity in phenylpropanoid pathway with a designed biosensor |
| Q36176596 | In vivo visualization of type II plasmid segregation: bacterial actin filaments pushing plasmids |
| Q40389062 | Inhibition of CRISPR-Cas9 with Bacteriophage Proteins |
| Q64927546 | Inhibition of low-density lipoprotein receptor degradation with a cyclic peptide that disrupts the homodimerization of IDOL E3 ubiquitin ligase. |
| Q28257999 | Intracellular detection and evolution of site-specific proteases using a genetic selection system |
| Q33570133 | Intracellular hydrogen peroxide and superoxide poison 3-deoxy-D-arabinoheptulosonate 7-phosphate synthase, the first committed enzyme in the aromatic biosynthetic pathway of Escherichia coli |
| Q54348862 | Involvement of AtoSC two-component system in Escherichia coli flagellar regulon. |
| Q42126464 | Involvement of Escherichia coli DNA polymerase IV in tolerance of cytotoxic alkylating DNA lesions in vivo. |
| Q36996756 | Knock-in/Knock-out (KIKO) vectors for rapid integration of large DNA sequences, including whole metabolic pathways, onto the Escherichia coli chromosome at well-characterised loci |
| Q36209777 | Long-Term Stable and Tightly Controlled Expression of Recombinant Proteins in Antibiotics-Free Conditions |
| Q41815173 | LytM-domain factors are required for daughter cell separation and rapid ampicillin-induced lysis in Escherichia coli. |
| Q37622760 | MISSA 2.0: an updated synthetic biology toolbox for assembly of orthogonal CRISPR/Cas systems |
| Q83118651 | MISSA is a highly efficient in vivo DNA assembly method for plant multiple-gene transformation |
| Q37418527 | Manganese import is a key element of the OxyR response to hydrogen peroxide in Escherichia coli |
| Q51363477 | MarRA, SoxSR, and Rob encode a signal dependent regulatory network in Escherichia coli. |
| Q41694474 | MazF activation promotes translational heterogeneity of the grcA mRNA in Escherichia coli populations. |
| Q86382031 | Metabolic engineering of Escherichia coli to produce zeaxanthin |
| Q33519503 | Mobile antibiotic resistance encoding elements promote their own diversity |
| Q50238026 | Molecular Cloning Designer Simulator (MCDS): All-in-one molecular cloning and genetic engineering design, simulation and management software for complex synthetic biology and metabolic engineering projects. |
| Q93221698 | Molecular and Functional Insights into the Regulation of d-Galactonate Metabolism by the Transcriptional Regulator DgoR in Escherichia coli |
| Q46406220 | Molecular characterization and verification of azido-3,8-dideoxy-d-manno-oct-2-ulosonic acid incorporation into bacterial lipopolysaccharide |
| Q33210306 | Molecular cloning, sequence analysis, and heterologous expression of the phosphinothricin tripeptide biosynthetic gene cluster from Streptomyces viridochromogenes DSM 40736. |
| Q37328191 | Molecular geometry of CsrA (RsmA) binding to RNA and its implications for regulated expression |
| Q48515695 | Mu-driven transposition of recombinant mini-Mu unit DNA in the Corynebacterium glutamicum chromosome |
| Q90001385 | Multidrug Resistance Regulators MarA, SoxS, Rob, and RamA Repress Flagellar Gene Expression and Motility in Salmonella enterica Serovar Typhimurium |
| Q44594054 | Mycobacterium smegmatis BioQ defines a new regulatory network for biotin metabolism |
| Q33979263 | Mycobacterium tuberculosis Ku can bind to nuclear DNA damage and sensitize mammalian cells to bleomycin sulfate |
| Q40545064 | Mycobacterium tuberculosis and Mycobacterium marinum non-homologous end-joining proteins can function together to join DNA ends in Escherichia coli |
| Q37200759 | New methods for tightly regulated gene expression and highly efficient chromosomal integration of cloned genes for Methanosarcina species. |
| Q90057425 | Nitric oxide disrupts bacterial cytokinesis by poisoning purine metabolism |
| Q41911689 | NlpD links cell wall remodeling and outer membrane invagination during cytokinesis in Escherichia coli |
| Q38792216 | Novel Technologies for Optimal Strain Breeding |
| Q27675754 | Nuclear Magnetic Resonance Solution Structure of the Peptidoglycan-Binding SPOR Domain from Escherichia coli DamX: Insights into Septal Localization |
| Q60303471 | ORBIT: a New Paradigm for Genetic Engineering of Mycobacterial Chromosomes |
| Q47929529 | Operon structure and cotranslational subunit association direct protein assembly in bacteria. |
| Q39722401 | Optimization and Characterization of the Synthetic Secondary Chromosome synVicII in Escherichia coli |
| Q58749112 | Overcoming the Cost of Positive Autoregulation by Accelerating the Response with a Coupled Negative Feedback |
| Q35626014 | Oxygen-Dependent Cell-to-Cell Variability in the Output of the Escherichia coli Tor Phosphorelay |
| Q54473561 | P1 plasmid partition: in vivo evidence for the ParA- and ParB-mediated formation of an anchored parS complex in the absence of a partner parS. |
| Q30536933 | Parallel in vivo DNA assembly by recombination: experimental demonstration and theoretical approaches |
| Q34150786 | Pathogenicity-associated islands in extraintestinal pathogenic Escherichia coli are fitness elements involved in intestinal colonization |
| Q36156174 | Pathway and enzyme redundancy in putrescine catabolism in Escherichia coli |
| Q34050856 | PdhR, the pyruvate dehydrogenase repressor, does not regulate lipoic acid synthesis |
| Q91701461 | Perforin-2 Breaches the Envelope of Phagocytosed Bacteria Allowing Antimicrobial Effectors Access to Intracellular Targets |
| Q97568978 | Phenotypic effects of paralogous ribosomal proteins bL31A and bL31B in E. coli |
| Q42929612 | Pho regulon promoter-mediated transcription of the key pathway gene aroG Fbr improves the performance of an l-phenylalanine-producing Escherichia coli strain |
| Q92641059 | PhoP-Mediated Repression of the SPI1 Type 3 Secretion System in Salmonella enterica Serovar Typhimurium |
| Q42463484 | Phosphorylation-independent dimer-dimer interactions by the enhancer-binding activator NtrC of Escherichia coli: a third function for the C-terminal domain. |
| Q36227468 | Physiological Roles and Adverse Effects of the Two Cystine Importers of Escherichia coli |
| Q39839158 | Plasmid DNA fermentation strain and process‐specific effects on vector yield, quality, and transgene expression |
| Q41451057 | Potent transcriptional interference by pausing of RNA polymerases over a downstream promoter |
| Q34112935 | Prion propagation can occur in a prokaryote and requires the ClpB chaperone |
| Q97686632 | Production of 1-octanol in Escherichia coli by a high flux thioesterase route |
| Q37582354 | Production of shikimic acid from Escherichia coli through chemically inducible chromosomal evolution and cofactor metabolic engineering |
| Q47103686 | Programmable DNA looping using engineered bivalent dCas9 complexes |
| Q91595611 | Programmable bacteria induce durable tumor regression and systemic antitumor immunity |
| Q30367608 | Promoter activation by CII, a potent transcriptional activator from bacteriophage 186. |
| Q35947400 | Protection against Shiga-Toxigenic Escherichia coli by Non-Genetically Modified Organism Receptor Mimic Bacterial Ghosts |
| Q37075579 | Purine utilization by Klebsiella oxytoca M5al: genes for ring-oxidizing and -opening enzymes |
| Q36788303 | Putrescine catabolism is a metabolic response to several stresses in Escherichia coli. |
| Q48205353 | Quantifying cellular capacity identifies gene expression designs with reduced burden |
| Q33691864 | Quantitative Kinetic Analyses of Shutting Off a Two-Component System |
| Q48733771 | Quantitative estimation of activity and quality for collections of functional genetic elements |
| Q92500899 | RNA polymerase pausing at a protein roadblock can enhance transcriptional interference by promoter occlusion |
| Q44724087 | Random mutagenesis identifies factors involved in formate-dependent growth of the methanogenic archaeon Methanococcus maripaludis |
| Q92161127 | Rational development of transformation in Clostridium thermocellum ATCC 27405 via complete methylome analysis and evasion of native restriction-modification systems |
| Q41831017 | Reciprocal Regulation of l-Arabinose and d-Xylose Metabolism in Escherichia coli |
| Q57094470 | Redefinition and Unification of the SXT/R391 Family of Integrative and Conjugative Elements |
| Q92459626 | Regulation of Iron Storage by CsrA Supports Exponential Growth of Escherichia coli |
| Q49316786 | Regulation of metabolism in Escherichia coli during growth on mixtures of the non-glucose sugars: arabinose, lactose, and xylose. |
| Q34312265 | Regulation of the Escherichia coli HipBA toxin-antitoxin system by proteolysis |
| Q35144337 | Repetitive genomic insertion of gene-sized dsDNAs by targeting the promoter region of a counter-selectable marker |
| Q35659811 | Replication and Active Partition of Integrative and Conjugative Elements (ICEs) of the SXT/R391 Family: The Line between ICEs and Conjugative Plasmids Is Getting Thinner. |
| Q35759476 | Repression of the inner membrane lipoprotein NlpA by Rns in enterotoxigenic Escherichia coli |
| Q51344618 | Repurposing site-specific recombinases for synthetic biology. |
| Q51622296 | Revisiting demand rules for gene regulation. |
| Q42105686 | RodZ (YfgA) is required for proper assembly of the MreB actin cytoskeleton and cell shape in E. coli. |
| Q37191525 | Role of FimW, FimY, and FimZ in regulating the expression of type i fimbriae in Salmonella enterica serovar Typhimurium |
| Q33339832 | Role of global regulators and nucleotide metabolism in antibiotic tolerance in Escherichia coli |
| Q42072775 | Role of the extracytoplasmic function protein family sigma factor RpoE in metal resistance of Escherichia coli |
| Q35095867 | Role of the mar-sox-rob regulon in regulating outer membrane porin expression |
| Q34453150 | Roles for both FtsA and the FtsBLQ subcomplex in FtsN-stimulated cell constriction in Escherichia coli. |
| Q34555106 | RtsA coordinately regulates DsbA and the Salmonella pathogenicity island 1 type III secretion system |
| Q37719214 | Salmonella enterica Serovar Typhi Lipopolysaccharide O-Antigen Modification Impact on Serum Resistance and Antibody Recognition |
| Q28766733 | Salmonella enterica serovar Typhimurium periplasmic superoxide dismutase SodCI is a member of the PhoPQ regulon and is induced in macrophages |
| Q36326607 | Salmonella genomic island 1 (SGI1) reshapes the mating apparatus of IncC conjugative plasmids to promote self-propagation. |
| Q42688968 | Self-enhanced accumulation of FtsN at Division Sites and Roles for Other Proteins with a SPOR domain (DamX, DedD, and RlpA) in Escherichia coli cell constriction |
| Q47254650 | Sexual recombination and increased mutation rate expedite evolution of Escherichia coli in varied fitness landscapes |
| Q35943400 | Similarity of tetracycline resistance genes isolated from fish farm bacteria to those from clinical isolates |
| Q50956257 | Single cell super-resolution imaging of E. coli OmpR during environmental stress. |
| Q83232366 | Single cell, super-resolution imaging reveals an acid pH-dependent conformational switch in SsrB regulates SPI-2 |
| Q33760274 | Site-specific chromosomal integration of large synthetic constructs |
| Q41518834 | Species-specific type II restriction-modification system of Xylella fastidiosa temecula1. |
| Q52653731 | Specific features of L-histidine production by Escherichia coli concerned with feedback control of AICAR formation and inorganic phosphate/metal transport. |
| Q83864142 | Strain engineering by genome mass transfer: efficient chromosomal trait transfer method utilizing donor genomic DNA and recipient recombineering hosts |
| Q42420724 | Strong stimulation of recombinant protein production in Escherichia coli by combining stimulatory control elements in an expression cassette |
| Q33585996 | Structure-function analysis of IntDOT. |
| Q27678759 | Structure-function analysis of the LytM domain of EnvC, an activator of cell wall remodelling at theEscherichia colidivision site |
| Q37065870 | Superoxide poisons mononuclear iron enzymes by causing mismetallation |
| Q90672397 | Synthetic control of plasmid replication enables target- and self-curing of vectors and expedites genome engineering of Pseudomonas putida |
| Q37379498 | Systematic phenome analysis of Escherichia coli multiple-knockout mutants reveals hidden reactions in central carbon metabolism. |
| Q35577950 | TatBC-independent TatA/Tat substrate interactions contribute to transport efficiency |
| Q35660182 | Temporal hierarchy of gene expression mediated by transcription factor binding affinity and activation dynamics |
| Q35902017 | Testing constraints on rRNA bases that make nonsequence-specific contacts with the codon-anticodon complex in the ribosomal A site. |
| Q35654507 | The DnaA Protein Is Not the Limiting Factor for Initiation of Replication in Escherichia coli. |
| Q27653378 | The Escherichia coli Cell Division Protein and Model Tat Substrate SufI (FtsP) Localizes to the Septal Ring and Has a Multicopper Oxidase-Like Structure |
| Q33541401 | The Escherichia coli mqsR and ygiT genes encode a new toxin-antitoxin pair |
| Q34467289 | The Escherichia coli small protein MntS and exporter MntP optimize the intracellular concentration of manganese |
| Q28492915 | The Salmonella SPI1 type three secretion system responds to periplasmic disulfide bond status via the flagellar apparatus and the RcsCDB system |
| Q28485717 | The Vibrio cholerae fatty acid regulatory protein, FadR, represses transcription of plsB, the gene encoding the first enzyme of membrane phospholipid biosynthesis |
| Q37539498 | The Virulence Regulator Rns Activates the Expression of CS14 Pili. |
| Q35095921 | The YaaA protein of the Escherichia coli OxyR regulon lessens hydrogen peroxide toxicity by diminishing the amount of intracellular unincorporated iron |
| Q42020372 | The alternative aerobic ribonucleotide reductase of Escherichia coli, NrdEF, is a manganese-dependent enzyme that enables cell replication during periods of iron starvation |
| Q39093135 | The association of the cytoplasmic domains of interleukin 4 receptor alpha and interleukin 13 receptor alpha 2 regulates interleukin 4 signaling |
| Q34303329 | The beta-oxidation systems of Escherichia coli and Salmonella enterica are not functionally equivalent |
| Q92767745 | The emergence of the two cell fates and their associated switching for a negative auto-regulating gene |
| Q37516465 | The htx and ptx operons of Pseudomonas stutzeri WM88 are new members of the pho regulon |
| Q35602469 | The induction of two biosynthetic enzymes helps Escherichia coli sustain heme synthesis and activate catalase during hydrogen peroxide stress |
| Q42038686 | The leucine-responsive regulatory protein, Lrp, modulates microcin J25 intrinsic resistance in Escherichia coli by regulating expression of the YojI microcin exporter |
| Q35361457 | The master activator of IncA/C conjugative plasmids stimulates genomic islands and multidrug resistance dissemination |
| Q38061976 | The molecular toolbox for chromosomal heterologous multiprotein expression in Escherichia coli |
| Q35133896 | The pathogen-associated iroA gene cluster mediates bacterial evasion of lipocalin 2. |
| Q39332980 | The response regulator SsrB activates expression of diverse Salmonella pathogenicity island 2 promoters and counters silencing by the nucleoid-associated protein H-NS. |
| Q39170398 | The role of repressor kinetics in relief of transcriptional interference between convergent promoters |
| Q51623723 | The small membrane protein MgrB regulates PhoQ bifunctionality to control PhoP target gene expression dynamics. |
| Q41768353 | The tib adherence locus of enterotoxigenic Escherichia coli is regulated by cyclic AMP receptor protein. |
| Q40340387 | Transcriptional Repression of the VC2105 Protein by Vibrio FadR Suggests that It Is a New Auxiliary Member of the fad Regulon |
| Q36197524 | Transcriptional cross talk within the mar-sox-rob regulon in Escherichia coli is limited to the rob and marRAB operons |
| Q36506158 | Transcriptional modulation of enterotoxigenic Escherichia coli virulence genes in response to epithelial cell interactions |
| Q40947162 | Transcriptional regulation of sitABCD of Salmonella enterica serovar Typhimurium by MntR and Fur |
| Q36964489 | Transcriptional regulation of subclass 5b fimbriae |
| Q54537142 | Transcriptome analysis of all two-component regulatory system mutants of Escherichia coli K-12. |
| Q41546256 | Translational Repression of the RpoS Antiadapter IraD by CsrA Is Mediated via Translational Coupling to a Short Upstream Open Reading Frame. |
| Q40345877 | Translational repression of NhaR, a novel pathway for multi-tier regulation of biofilm circuitry by CsrA |
| Q36170860 | Twin-arginine translocase mutations that suppress folding quality control and permit export of misfolded substrate proteins |
| Q34864912 | Two groups of phenylalanine biosynthetic operon leader peptides genes: a high level of apparently incidental frameshifting in decoding Escherichia coli pheL. |
| Q58699951 | Type and capacity of glucose transport influences succinate yield in two-stage cultivations |
| Q34111754 | Uropathogenic Escherichia coli flagella aid in efficient urinary tract colonization |
| Q39564896 | Use of new methods for construction of tightly regulated arabinose and rhamnose promoter fusions in studies of the Escherichia coli phosphate regulon. |
| Q35748055 | Use of transposase and ends of IS608 enables precise and scarless genome modification for modulating gene expression and metabolic engineering applications in Escherichia coli |
| Q35738580 | Using protein abundance to indicate underlying mRNA expression levels in E.coli: an SEM modelling approach |
| Q35192447 | Using superfolder green fluorescent protein for periplasmic protein localization studies |
| Q45861988 | Vector insert-targeted integrative antisense expression system for plasmid stabilization |
| Q56895133 | Visualizing evolution in real time to determine the molecular mechanisms of n-butanol tolerance in Escherichia coli |
| Q38751916 | ZapA and ZapB form an FtsZ-independent structure at midcell. |
| Q45957295 | [Cloning, expression and comparative analysis of peroxiredoxine 6 from different species] |
| Q44605232 | β-Ketoacyl-Acyl Carrier Protein Synthase III (FabH) Is Essential for Bacterial Fatty Acid Synthesis |
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