scholarly article | Q13442814 |
P356 | DOI | 10.1126/SCIENCE.7681219 |
P953 | full work available at URL | https://www.science.org/doi/pdf/10.1126/science.7681219 |
P698 | PubMed publication ID | 7681219 |
P50 | author | Maria Mercedes Zambrano | Q58913089 |
P2093 | author name string | R. Kolter | |
D. A. Siegele | |||
M. Almirón | |||
A. Tormo | |||
P2860 | cites work | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
Starvation proteins in Escherichia coli: kinetics of synthesis and role in starvation survival | Q39961383 | ||
Nucleotide sequence of katF of Escherichia coli suggests KatF protein is a novel sigma transcription factor | Q40539667 | ||
Experimental evidence for an alternative to directed mutation in the bgl operon | Q41115000 | ||
Rapid evolution in response to high-temperature selection | Q46330296 | ||
Catalases HPI and HPII in Escherichia coli are induced independently. | Q54790507 | ||
New Tn10 derivatives for transposon mutagenesis and for construction of lacZ operon fusions by transposition | Q72413204 | ||
Selection in chemostats | Q24654595 | ||
Identification of a central regulator of stationary-phase gene expression inEscherichia coli | Q27976519 | ||
The origin of mutants | Q28288915 | ||
Azthreonam (SQ 26,776), a synthetic monobactam specifically active against aerobic gram-negative bacteria | Q34274482 | ||
Life after log | Q36109652 | ||
Global control in Salmonella typhimurium: two-dimensional electrophoretic analysis of starvation-, anaerobiosis-, and heat shock-inducible proteins | Q36259098 | ||
The molecular basis of carbon-starvation-induced general resistance in Escherichia coli | Q37688891 | ||
Genetic basis of starvation survival in nondifferentiating bacteria | Q38208149 | ||
Structure and function of bacterial sigma factors | Q39532182 | ||
Genetics of endospore formation in Bacillus subtilis | Q39593172 | ||
The transient phase between growth and nongrowth of heterotrophic bacteria, with emphasis on the marine environment | Q39683451 | ||
The putative sigma factor KatF has a central role in development of starvation-mediated general resistance in Escherichia coli | Q39942213 | ||
Growth phase-regulated expression of bolA and morphology of stationary-phase Escherichia coli cells are controlled by the novel sigma factor sigma S. | Q39942389 | ||
Stationary-phase-inducible "gearbox" promoters: differential effects of katF mutations and role of sigma 70 | Q39942395 | ||
Trehalose synthesis genes are controlled by the putative sigma factor encoded by rpoS and are involved in stationary-phase thermotolerance in Escherichia coli | Q39958318 | ||
P433 | issue | 5102 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Escherichia coli | Q25419 |
P304 | page(s) | 1757-1760 | |
P577 | publication date | 1993-03-01 | |
1993-03-19 | |||
P1433 | published in | Science | Q192864 |
P1476 | title | Microbial competition: Escherichia coli mutants that take over stationary phase cultures | |
Microbial Competition: Escherichia coli Mutants That Take Over Stationary Phase Cultures | |||
P478 | volume | 259 |
Q47341992 | 100 Days of marine Synechococcus-Ruegeria pomeroyi interaction: A detailed analysis of the exoproteome. |
Q35892783 | 6S RNA function enhances long-term cell survival |
Q34697038 | 6S RNA regulation of pspF transcription leads to altered cell survival at high pH. |
Q42948978 | A DNA polymerase V homologue encoded by TOL plasmid pWW0 confers evolutionary fitness on Pseudomonas putida under conditions of environmental stress |
Q91969400 | A Mutant RNA Polymerase Activates the General Stress Response, Enabling Escherichia coli Adaptation to Late Prolonged Stationary Phase |
Q33994535 | A carboxy-terminal 16-amino-acid region of sigma(38) of Escherichia coli is important for transcription under high-salt conditions and sigma activities in vivo. |
Q54515474 | A comparative study of variation in codon 33 of the rpoS gene in Escherichia coli K12 stocks: implications for the synthesis of σs |
Q42968100 | A genetic strategy to demonstrate the occurrence of spontaneous mutations in nondividing cells within colonies of Escherichia coli |
Q39361826 | A hypervariable 130-kilobase genomic region of Magnetospirillum gryphiswaldense comprises a magnetosome island which undergoes frequent rearrangements during stationary growth |
Q49851989 | A network of regulators promotes dehydration tolerance in Escherichia coli. |
Q40001101 | A regulatory trade-off as a source of strain variation in the species Escherichia coli |
Q37426997 | A replication clock for Mycobacterium tuberculosis |
Q37191713 | A role for single-stranded exonucleases in the use of DNA as a nutrient |
Q41815880 | A stop codon-dependent internal secondary translation initiation region in Escherichia coli rpoS. |
Q80092504 | Accumulation of hns mutations specifically in stationary phase in an E. coli strain carrying an impaired rpoS locus |
Q35295130 | Acetate availability and utilization supports the growth of mutant sub-populations on aging bacterial colonies |
Q54636621 | Acinetobacter baylyi long-term stationary-phase protein StiP is a protease required for normal cell morphology and resistance to tellurite. |
Q33590500 | Acinetobacter baylyi starvation-induced genes identified through incubation in long-term stationary phase |
Q35668145 | Activation of the cryptic PhnE permease promotes rapid adaptive evolution in a population of Escherichia coli K-12 starved for phosphate |
Q37685579 | Adaptation of Escherichia coli to Long-Term Serial Passage in Complex Medium: Evidence of Parallel Evolution |
Q39547256 | Adaptation of Mycobacterium smegmatis to stationary phase. |
Q38059441 | Adaptation of Pseudomonas aeruginosa to the cystic fibrosis airway: an evolutionary perspective |
Q34159691 | Adaptation to famine: a family of stationary-phase genes revealed by microarray analysis |
Q39847838 | Adaptation to nutrient starvation in Rhizobium leguminosarum bv. phaseoli: analysis of survival, stress resistance, and changes in macromolecular synthesis during entry to and exit from stationary phase. |
Q34130237 | Adaptive evolution of the lactose utilization network in experimentally evolved populations of Escherichia coli. |
Q38118393 | Adaptive laboratory evolution -- principles and applications for biotechnology |
Q93084901 | Aging of a Bacterial Colony Enforces the Evolvement of Nondifferentiating Mutants |
Q39679204 | Alcohol-induced delay of viability loss in stationary-phase cultures of Escherichia coli |
Q36369411 | An analogy between the evolution of drug resistance in bacterial communities and malignant tissues |
Q38011620 | An evolutionary view of plant tissue culture: somaclonal variation and selection |
Q30502354 | Anomalous spatial redistribution of competing bacteria under starvation conditions |
Q34158265 | Antagonistic regulation of motility and transcriptome expression by RpoN and RpoS in Escherichia coli. |
Q41411619 | Antiglycation Effects of Carnosine and Other Compounds on the Long-Term Survival of Escherichia coli |
Q45162465 | Appropriate Regulation of the σE-Dependent Envelope Stress Response Is Necessary To Maintain Cell Envelope Integrity and Stationary-Phase Survival in Escherichia coli. |
Q33830368 | Assessing chronological aging in bacteria |
Q27006977 | Bacteria and game theory: the rise and fall of cooperation in spatially heterogeneous environments |
Q90730474 | Bacterial Longevity Requires Protein Synthesis and a Stringent Response |
Q28534615 | Bacterial adaptation through loss of function |
Q34618065 | Bacterial evolution through the selective loss of beneficial Genes. Trade-offs in expression involving two loci. |
Q77910540 | Bacterial gene products in response to near-ultraviolet radiation |
Q38103942 | Bacterial genome evolution within a clonal population: from in vitro investigations to in vivo observations |
Q43358488 | Bacterial invasion potential in water is determined by nutrient availability and the indigenous community |
Q24675317 | Bacterial metapopulations in nanofabricated landscapes |
Q34300761 | Biochemistry and comparative genomics of SxxK superfamily acyltransferases offer a clue to the mycobacterial paradox: presence of penicillin-susceptible target proteins versus lack of efficiency of penicillin as therapeutic agent |
Q33330202 | Cell division in Escherichia coli cultures monitored at single cell resolution |
Q41842990 | Changes in barotolerance, thermotolerance, and cellular morphology throughout the life cycle of Listeria monocytogenes |
Q50119830 | Changes in viability and macromolecular content of long-term batch cultures of Salmonella typhimurium measured by flow cytometry |
Q35507010 | Characterization of the acid resistance phenotype and rpoS alleles of shiga-like toxin-producing Escherichia coli |
Q39494708 | Characterization of the ssnA gene, which is involved in the decline of cell viability at the beginning of stationary phase in Escherichia coli. |
Q39565257 | Characterization of the starvation-survival response of Staphylococcus aureus. |
Q37957577 | Chronological aging in Saccharomyces cerevisiae |
Q50134723 | Comparative study of the protective effect against Salmonella colonisation in newly hatched SPF chickens using live, attenuated Salmonella vaccine strains, wild-type Salmonella strains or a competitive exclusion product |
Q36878608 | Competitive fitness during feast and famine: how SOS DNA polymerases influence physiology and evolution in Escherichia coli |
Q38446575 | Competitive growth advantage of nontoxigenic mutants in the stationary phase in archival cultures of pathogenic Vibrio cholerae strains |
Q36440234 | Composting: a potentially safe process for disposal of genetically modified organisms |
Q37011224 | Computation of mutual fitness by competing bacteria |
Q34098538 | Construction of soluble adenylyl cyclase from human membrane-bound type 7 adenylyl cyclase |
Q91687834 | Continuous Culture Adaptation of Methylobacterium extorquens AM1 and TK 0001 to Very High Methanol Concentrations |
Q28547287 | Controlled Measurement and Comparative Analysis of Cellular Components in E. coli Reveals Broad Regulatory Changes in Response to Glucose Starvation |
Q36961674 | Controlling mutation: intervening in evolution as a therapeutic strategy |
Q35162003 | CsrA regulates translation of the Escherichia coli carbon starvation gene, cstA, by blocking ribosome access to the cstA transcript |
Q30769462 | Cultivation-independent, semiautomatic determination of absolute bacterial cell numbers in environmental samples by fluorescence in situ hybridization |
Q38319171 | Culture volume and vessel affect long-term survival, mutation frequency, and oxidative stress of Escherichia coli |
Q40024302 | Cyclopropane ring formation in membrane lipids of bacteria. |
Q22065463 | DNA as a Nutrient: Novel Role for Bacterial Competence Gene Homologs |
Q39566269 | DNA synthesis and viability of a mutT derivative of Escherichia coli WP2 under conditions of amino acid starvation and relation to stationary-phase (adaptive) mutation. |
Q35583474 | Death's toolbox: examining the molecular components of bacterial programmed cell death |
Q34725734 | Decay of unused characters by selection and drift |
Q38504198 | Degradation of Toluene and Trichloroethylene by Burkholderia cepacia G4 in Growth-Limited Fed-Batch Culture. |
Q42323318 | Density-Dependent Recycling Promotes the Long-Term Survival of Bacterial Populations during Periods of Starvation |
Q35097363 | Density-dependent sorting of physiologically different cells of Vibrio parahaemolyticus |
Q35681764 | Detection of two smooth colony phenotypes in a Salmonella enteritidis isolate which vary in their ability to contaminate eggs |
Q36196194 | Development of a Novel Plasmid-Free Thymidine Producer by Reprogramming Nucleotide Metabolic Pathways. |
Q39680847 | Different spectra of stationary-phase mutations in early-arising versus late-arising mutants of Pseudomonas putida: involvement of the DNA repair enzyme MutY and the stationary-phase sigma factor RpoS. |
Q35631720 | Differential protease-mediated turnover of H-NS and StpA revealed by a mutation altering protein stability and stationary-phase survival of Escherichia coli |
Q39679614 | Differential spectrum of mutations that activate the Escherichia coli bgl operon in an rpoS genetic background |
Q51432609 | Differential stress resistance and metabolic traits underlie coexistence in a sympatrically evolved bacterial population. |
Q73840629 | Disappearance of growth advantage in stationary phase (GASP) phenomenon under a high magnetic field |
Q33309765 | Diversification rates increase with population size and resource concentration in an unstructured habitat |
Q57014648 | Diversity emerging: from competitive exclusion to neutral coexistence in ecosystems |
Q24564681 | Dps protects cells against multiple stresses during stationary phase |
Q59315198 | Dynamics of bacterial populations in relation to carbon availability in a residue-amended soil |
Q39801105 | E. coli hypoxia-inducible factor ArcA mediates lifespan extension in a lipoic acid synthase mutant by suppressing acetyl-CoA synthetase |
Q38202864 | Ecological and temporal constraints in the evolution of bacterial genomes. |
Q42460686 | Effect of endogenous carotenoids and defective RpoS sigma factor on spontaneous mutation under starvation conditions in Escherichia coli: evidence for the possible involvement of singlet oxygen |
Q28346858 | Effect of endogenous carotenoids on "adaptive" mutation in Escherichia coli FC40 |
Q33257910 | Effect of random and hub gene disruptions on environmental and mutational robustness in Escherichia coli |
Q38485876 | Effect of trichloroethylene on the competitive behavior of toluene-degrading bacteria |
Q51717665 | Emergence of variants with altered survival properties in stationary phase cultures of Campylobacter jejuni. |
Q34697000 | Escherichia coli competence gene homologs are essential for competitive fitness and the use of DNA as a nutrient |
Q36358510 | Escherichia coli lacking RpoS are rare in natural populations of non-pathogens |
Q36121806 | Escherichia coli mutants lacking NADH dehydrogenase I have a competitive disadvantage in stationary phase |
Q35075254 | Essential role of flavohemoglobin in long-term anaerobic survival of Bacillus subtilis |
Q93014967 | Eukaryotic Adaptation to Years-Long Starvation Resembles that of Bacteria |
Q36456226 | Evolution of microbial diversity during prolonged starvation |
Q54385309 | Evolution of the RpoS regulon: origin of RpoS and the conservation of RpoS-dependent regulation in bacteria. |
Q35751528 | Evolutionary Consequence of a Trade-Off between Growth and Maintenance along with Ribosomal Damages |
Q34612728 | Evolutionary cheating in Escherichia coli stationary phase cultures |
Q34937408 | Evolutionary dynamics of bacteria in a human host environment |
Q24564036 | Evolutionary genomics of ecological specialization |
Q37983903 | Evolutionary insight from whole-genome sequencing of experimentally evolved microbes. |
Q47928367 | Evolutionary loss of the rdar morphotype in Salmonella as a result of high mutation rates during laboratory passage |
Q33584235 | Expanding the RpoS/σS-network by RNA sequencing and identification of σS-controlled small RNAs in Salmonella |
Q64993466 | Experimental Evolution of Escherichia coli K-12 at High pH and with RpoS Induction. |
Q38683209 | Experimental evolution and the dynamics of adaptation and genome evolution in microbial populations |
Q39485954 | Expression of the antifeeding gene anfA1 in Serratia entomophila requires rpoS. |
Q57719565 | Factors affecting the emergence of pathogens on foods |
Q34569122 | Fitness of Outbreak and Environmental Strains of Escherichia coli O157:H7 in Aerosolizable Soil and Association of Clonal Variation in Stress Gene Regulation |
Q50118737 | Flow cytometry characterisation of Salmonella typhimurium mutants defective in proton translocating proteins and stationary-phase growth phenotype |
Q39500749 | Function of the sigma(E) regulon in dead-cell lysis in stationary-phase Escherichia coli |
Q34718799 | Functional heterogeneity of RpoS in stress tolerance of enterohemorrhagic Escherichia coli strains |
Q50102861 | GASP phenotype: presence in enterobacteria and independence of sigmaS in its acquisition. |
Q34388973 | GASPing for life in stationary phase |
Q34232088 | GacA regulates symbiotic colonization traits of Vibrio fischeri and facilitates a beneficial association with an animal host |
Q34643555 | General stress response regulator RpoS in adaptive mutation and amplification in Escherichia coli |
Q42570130 | Generation of metabolically diverse strains of Streptococcus pyogenes during survival in stationary phase. |
Q34280822 | Genes responsible for anaerobic fumarate and arginine metabolism are involved in growth suppression in Salmonella enterica serovar Typhimurium in vitro, without influencing colonisation inhibition in the chicken in vivo |
Q33747528 | Genetic Basis of Growth Adaptation of Escherichia coli after Deletion of pgi, a Major Metabolic Gene |
Q34614487 | Genetic architecture of thermal adaptation in Escherichia coli |
Q33207040 | Genetic diversity of Escherichia coli isolates in irrigation water and associated sediments: implications for source tracking |
Q40441694 | Genetic mechanisms involved in cellular recovery from oxidative stress |
Q28651650 | Genome dynamics during experimental evolution |
Q55386383 | Genome economization and a new approach to the species concept in bacteria. |
Q41746387 | Genome-Wide Transcriptional Response to Varying RpoS Levels in Escherichia coli K-12 |
Q33726346 | Genomewide Mutational Diversity in Escherichia coli Population Evolving in Prolonged Stationary Phase |
Q37513651 | Genomic changes arising in long-term stab cultures of Escherichia coli |
Q42711234 | Genotype-by-environment interactions influencing the emergence of rpoS mutations in Escherichia coli populations |
Q39538692 | Global adaptations resulting from high population densities in Escherichia coli cultures |
Q42565092 | Global analysis of proteins synthesized by Mycobacterium smegmatis provides direct evidence for physiological heterogeneity in stationary-phase cultures. |
Q33654823 | Global gene expression analysis of long-term stationary phase effects in E. coli K12 MG1655 |
Q39493943 | Growth in studying the cessation of growth. |
Q36574440 | Growth phase-dependent transcription of the sigma(54)-dependent Po promoter controlling the Pseudomonas-derived (methyl)phenol dmp operon of pVI150 |
Q37342706 | Growth phenotypes of Pseudomonas aeruginosa lasR mutants adapted to the airways of cystic fibrosis patients |
Q39841506 | Growth suppression in early-stationary-phase nutrient broth cultures of Salmonella typhimurium and Escherichia coli is genus specific and not regulated by sigma S. |
Q49928155 | High Phenotypic Variability among Representative Strains of Common Salmonella enterica Serovars with Possible Implications for Food Safety |
Q55285004 | High mutation rates limit evolutionary adaptation in Escherichia coli. |
Q34097880 | How molecular competition influences fluxes in gene expression networks |
Q34448396 | Hungry bacteria--definition and properties of a nutritional state |
Q28776505 | Hypermutation in derepressed operons of Escherichia coli K12 |
Q39568776 | Identification of conserved, RpoS-dependent stationary-phase genes of Escherichia coli. |
Q30401332 | Inactivation of Transcriptional Regulators during Within-Household Evolution of Escherichia coli |
Q42845393 | Influence of amino acids on low-density Escherichia coli responses to nutrient downshifts. |
Q33988222 | Influence of infected cell growth state on bacteriophage reactivation levels. |
Q35603428 | Inorganic polyphosphate supports resistance and survival of stationary-phase Escherichia coli |
Q30011213 | Insertion sequence-related genetic variation in resting Escherichia coli K-12. |
Q41992183 | Insertion-sequence-mediated mutations isolated during adaptation to growth and starvation in Lactococcus lactis |
Q38957822 | Intergenic sequence comparison of Escherichia coli isolates reveals lifestyle adaptations but not host specificity. |
Q34001674 | Intracellular growth in Acanthamoeba castellanii affects monocyte entry mechanisms and enhances virulence of Legionella pneumophila. |
Q43969685 | Involvement of caspase-3-like protein in rapid cell death of Xanthomonas |
Q41873944 | Involvement of the global regulator H-NS in the survival of Escherichia coli in stationary phase |
Q26828792 | Life under extreme energy limitation: a synthesis of laboratory- and field-based investigations |
Q27316309 | Lineage Tracking for Probing Heritable Phenotypes at Single-Cell Resolution |
Q39472443 | Listeria monocytogenes adapts to long-term stationary phase survival without compromising bacterial virulence |
Q36369839 | Long-term survival during stationary phase: evolution and the GASP phenotype |
Q41729709 | Low frequency of endospore-specific genes in subseafloor sedimentary metagenomes |
Q35198922 | Massive diversification in aging colonies of Escherichia coli |
Q26778679 | Mechanism to control the cell lysis and the cell survival strategy in stationary phase under heat stress |
Q22122024 | Microbial genetics: Evolution experiments with microorganisms: the dynamics and genetic bases of adaptation |
Q38074264 | Microbial life under extreme energy limitation. |
Q46252453 | Molecular Basis of Bacterial Longevity. |
Q48248666 | Molecular analysis of mutS expression and mutation in natural isolates of pathogenic Escherichia coli |
Q33716983 | Molecular and evolutionary bases of within-patient genotypic and phenotypic diversity in Escherichia coli extraintestinal infections |
Q33682035 | Molecular inroads into the regulation and metabolism of fatty acids, lessons from bacteria |
Q52183473 | Morphological adaptation and inhibition of cell division during stationary phase in Caulobacter crescentus. |
Q47986866 | Multicellular and aggregative behaviour of Salmonella typhimurium strains is controlled by mutations in the agfD promoter |
Q36683593 | Multiple Pathways of Genome Plasticity Leading to Development of Antibiotic Resistance. |
Q35869358 | Mutation as a stress response and the regulation of evolvability |
Q40897789 | Mutation of a LysR-type regulator of antifungal activity results in a growth advantage in stationary phase phenotype in Pseudomonas aureofaciens PA147-2. |
Q41194789 | Mutational Consequences of Ciprofloxacin in Escherichia coli |
Q33992996 | Mutations enhancing amino acid catabolism confer a growth advantage in stationary phase |
Q39891746 | Mutations that activate the silent bgl operon of Escherichia coli confer a growth advantage in stationary phase |
Q92450961 | Nanocalorimetry Reveals the Growth Dynamics of Escherichia coli Cells Undergoing Adaptive Evolution during Long-Term Stationary Phase |
Q42203307 | Near-zero growth kinetics of Pseudomonas putida deduced from proteomic analysis |
Q37674803 | New technologies in using recombinant attenuated Salmonella vaccine vectors |
Q93216327 | Nitrogen starvation reveals the mitotic potential of mutants in the S/MAPK pathways |
Q52620638 | Novel pathway directed by σ E to cause cell lysis in Escherichia coli. |
Q34491240 | Osmoporin OmpC forms a complex with MlaA to maintain outer membrane lipid asymmetry in Escherichia coli |
Q39488814 | Osmotic stress-induced genetic rearrangements in Escherichia coli H10407 detected by randomly amplified polymorphic DNA analysis |
Q42121314 | Overproduction of exopolysaccharides by an Escherichia coli K-12 rpoS mutant in response to osmotic stress |
Q42573563 | Oxygen consumption rates of bacteria under nutrient-limited conditions |
Q35530168 | Phenotypic diversity caused by differential RpoS activity among environmental Escherichia coli isolates |
Q35970077 | Phylogenetic and Functional Substrate Specificity for Endolithic Microbial Communities in Hyper-Arid Environments |
Q35759680 | Physiological effects of Crl in Salmonella are modulated by sigmaS level and promoter specificity |
Q58615356 | Physiological, Genetic, and Transcriptomic Analysis of Alcohol-Induced Delay of Bacterial Death in |
Q41903190 | Polymorphisms in rpoS and stress tolerance heterogeneity in natural isolates of Cronobacter sakazakii |
Q46541248 | Polyphasic classification of 0.2 microm filterable bacteria from the western Mediterranean Sea |
Q33963607 | Population dynamics of a Lac- strain of Escherichia coli during selection for lactose utilization |
Q39294414 | Probiotic properties of Oxalobacter formigenes: an in vitro examination |
Q34032667 | Problems posed by natural environments for monitoring microorganisms |
Q34469684 | Programmed and altruistic ageing |
Q34023671 | Programmed death in bacteria |
Q33603147 | Prolonged stationary-phase incubation selects for lrp mutations in Escherichia coli K-12 |
Q54254011 | Proteomics analysis of a long-term survival strain of Escherichia coli K-12 exhibiting a growth advantage in stationary-phase (GASP) phenotype. |
Q34478849 | Quorum sensing and multidrug transporters in Escherichia coli |
Q42227289 | Rapid Genetic Adaptation during the First Four Months of Survival under Resource Exhaustion |
Q35220658 | Rapid evolution of diminished transformability in Acinetobacter baylyi |
Q39741617 | Rapid protection of gnotobiotic pigs against experimental salmonellosis following induction of polymorphonuclear leukocytes by avirulent Salmonella enterica. |
Q38374770 | Regulation of gene expression: cryptic β-glucoside (bgl) operon of Escherichia coli as a paradigm |
Q43125839 | Replication bypass of interstrand cross-link intermediates by Escherichia coli DNA polymerase IV. |
Q35088972 | Repressor activity of the RpoS/σS-dependent RNA polymerase requires DNA binding |
Q39705931 | Resident parking only: rhamnolipids maintain fluid channels in biofilms. |
Q39929957 | Responses to nutrient starvation in Pseudomonas putida KT2442: analysis of general cross-protection, cell shape, and macromolecular content |
Q41815411 | Rich Medium Composition Affects Escherichia coli Survival, Glycation, and Mutation Frequency during Long-Term Batch Culture |
Q93132800 | Rock-paper-scissors: Engineered population dynamics increase genetic stability |
Q37033120 | Role of RpoS in the virulence of Citrobacter rodentium |
Q35098656 | Role of an Escherichia coli stress-response operon in stationary-phase survival |
Q35139140 | Role of high-fidelity Escherichia coli DNA polymerase I in replication bypass of a deoxyadenosine DNA-peptide cross-link |
Q34419246 | Role of rpoS in Escherichia coli O157:H7 strain H32 biofilm development and survival |
Q33739792 | Role of the Escherichia coli SurA protein in stationary-phase survival. |
Q36613324 | RpoS contributes to phagocyte oxidase-mediated stress resistance during urinary tract infection by Escherichia coli CFT073. |
Q41001242 | RpoS role in virulence and fitness in enteropathogenic Escherichia coli. |
Q35625190 | RpoS- and OxyR-independent induction of HPI catalase at stationary phase in Escherichia coli and identification of rpoS mutations in common laboratory strains |
Q34011945 | RpoS-dependent transcriptional control of sprE: regulatory feedback loop |
Q24530758 | SOS-induced DNA polymerases enhance long-term survival and evolutionary fitness |
Q36197324 | Salmonella stress management and its relevance to behaviour during intestinal colonisation and infection |
Q56975009 | Secretion of an antibacterial factor during resuscitation of dormant cells inMicrococcus luteus cultures held in an extended stationary phase |
Q41439355 | Selection for loss of RpoS in Cronobacter sakazakii by growth in the presence of acetate as a carbon source |
Q89653532 | Selection-Driven Gene Inactivation in Salmonella |
Q40408854 | Sigma s-dependent promoters in Escherichia coli are located in DNA regions with intrinsic curvature |
Q35027684 | Spatial structure facilitates cooperation in a social dilemma: empirical evidence from a bacterial community |
Q33700399 | Starvation for different nutrients in Escherichia coli results in differential modulation of RpoS levels and stability |
Q39572974 | Starvation selection restores elastase and rhamnolipid production in a Pseudomonas aeruginosa quorum-sensing mutant |
Q37710717 | Stationary phase in gram-negative bacteria. |
Q35544150 | Stationary phase mutagenesis: mechanisms that accelerate adaptation of microbial populations under environmental stress |
Q39587649 | Stationary-phase variation due to transposition of novel insertion elements in Xanthomonas oryzae pv. oryzae |
Q36023733 | Staying alive: metabolic adaptations to quiescence |
Q36007272 | Stress and how bacteria cope with death and survival. |
Q36321871 | Superoxide is a mediator of an altruistic aging program in Saccharomyces cerevisiae |
Q35594649 | Survival kinetics of starving bacteria is biphasic and density-dependent |
Q33989500 | Survival of Campylobacter jejuni during stationary phase: evidence for the absence of a phenotypic stationary-phase response |
Q43561492 | Survival of Escherichia coli during long-term starvation: effects of aeration, NaCl, and the rpoS and osmC gene products |
Q33941676 | Survival of Escherichia coli under lethal heat stress by L-form conversion |
Q39492823 | Survival response and rearrangement of plasmid DNA of Lactococcus lactis during long-term starvation |
Q36124805 | Synthesis of the stationary-phase sigma factor sigma s is positively regulated by ppGpp |
Q36924695 | The Aggregation of Brucella abortus Occurs Under Microaerobic Conditions and Promotes Desiccation Tolerance and Biofilm Formation. |
Q90226081 | The Antibiotic Trimethoprim Displays Strong Mutagenic Synergy with 2-Aminopurine |
Q38296490 | The C-terminal domain of Escherichia coli Hfq is required for regulation |
Q42275508 | The El Tor biotype of Vibrio cholerae exhibits a growth advantage in the stationary phase in mixed cultures with the classical biotype |
Q28830367 | The General Stress Response Is Conserved in Long-Term Soil-Persistent Strains of Escherichia coli |
Q33730748 | The L-isoaspartyl protein repair methyltransferase enhances survival of aging Escherichia coli subjected to secondary environmental stresses |
Q28487396 | The Mycobacterium tuberculosis mysB gene product is a functional equivalent of the Escherichia coli sigma factor, KatF |
Q49320136 | The Odyssey of the Ancestral Escherich Strain through Culture Collections: an Example of Allopatric Diversification |
Q34189650 | The RpoS-mediated general stress response in Escherichia coli |
Q54288482 | The effect of the rpoSam allele on gene expression and stress resistance in Escherichia coli. |
Q50042352 | The emergence of metabolic heterogeneity and diverse growth responses in isogenic bacterial cells |
Q34882929 | The genome-scale interplay amongst xenogene silencing, stress response and chromosome architecture in Escherichia coli |
Q42034744 | The global regulator Lrp contributes to mutualism, pathogenesis and phenotypic variation in the bacterium Xenorhabdus nematophila |
Q40345503 | The growth advantage in stationary-phase phenotype conferred by rpoS mutations is dependent on the pH and nutrient environment |
Q36812721 | The i6A37 tRNA modification is essential for proper decoding of UUX-Leucine codons during rpoS and iraP translation |
Q35665385 | The idiosyncrasy of spatial structure in bacterial competition |
Q39240966 | The impact of insertion sequences on bacterial genome plasticity and adaptability. |
Q34618621 | The importance of RpoS in the survival of bacteria through food processing. |
Q63363530 | The physiology and collective recalcitrance of microbial biofilm communities |
Q34618614 | The physiology of Campylobacter species and its relevance to their role as foodborne pathogens |
Q38924195 | The physiology of growth arrest: uniting molecular and environmental microbiology |
Q37029909 | The spread of a beneficial mutation in experimental bacterial populations: the influence of the environment and genotype on the fixation of rpoS mutations |
Q30492755 | The transcriptional programme of Salmonella enterica serovar Typhimurium reveals a key role for tryptophan metabolism in biofilms. |
Q33744199 | The two-component regulators GacS and GacA influence accumulation of the stationary-phase sigma factor sigmaS and the stress response in Pseudomonas fluorescens Pf-5 |
Q34070060 | The uncertain consequences of transferring bacterial strains between laboratories - rpoS instability as an example. |
Q40345257 | The β-glucoside (bgl) operon of Escherichia coli is involved in the regulation of oppA, encoding an oligopeptide transporter |
Q64107265 | Tracing the phylogenetic history of the Crl regulon through the Bacteria and Archaea genomes |
Q37543841 | Transcriptional occlusion caused by overlapping promoters. |
Q39483041 | Use of single-strand conformation polymorphism analysis to examine the variability of the rpoS sequence in environmental isolates of Salmonellae |
Q33287803 | Using expression arrays for copy number detection: an example from E. coli |
Q33769721 | Variation in acid resistance among shiga toxin-producing clones of pathogenic Escherichia coli |
Q39493024 | Variation in resistance to high hydrostatic pressure and rpoS heterogeneity in natural isolates of Escherichia coli O157:H7. |
Q34551450 | Vibrio cholerae classical biotype is converted to the viable non-culturable state when cultured with the El Tor biotype |
Q39517156 | Vibrio cholerae requires rpoS for efficient intestinal colonization |
Q46118605 | Vibrio fischeri exhibit the growth advantage in stationary-phase phenotype. |
Q50115837 | Virulence in the chick model and stress tolerance of Salmonella enterica serovar Orion var. 15+. |
Q36351996 | What is adaptation by natural selection? Perspectives of an experimental microbiologist |
Q36119166 | Why yeast cells can undergo apoptosis: death in times of peace, love, and war |
Q26307560 | Xenorhabdus bovienii |
Q27317431 | dsdA Does Not Affect Colonization of the Murine Urinary Tract by Escherichia coli CFT073 |
Q34004165 | rpoS gene function is a disadvantage for Escherichia coli BJ4 during competitive colonization of the mouse large intestine |
Q38464383 | rpoS mutants in archival cultures of Salmonella enterica serovar typhimurium |
Q34434398 | rpoS mutations and loss of general stress resistance in Escherichia coli populations as a consequence of conflict between competing stress responses |
Q38193405 | sigmaS, a major player in the response to environmental stresses in Escherichia coli: role, regulation and mechanisms of promoter recognition. |
Search more.