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Stationary-Phase Gene Regulation in Escherichia coli §

https://doi.org/10.1128/ecosalplus.5.6.3

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Outgoing claims: the papers this work cites, builds on, or argues with.

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Significance of rpoS during maturation of Escherichia coli biofilms

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HU and IHF, two homologous histone‐like proteins of Escherichia coli, form different protein‐DNA complexes with short DNA fragments.

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Quantitative control of the stationary phase‐specific sigma factor, sigma S, in Escherichia coli: involvement of the nucleoid protein H‐NS.

inferredcites →https://doi.org/10.1002/j.1460-2075.1996.tb00475.xopenalex-snapshot

The response regulator RssB controls stability of the sigma(S) subunit of RNA polymerase in Escherichia coli.

inferredcites →https://doi.org/10.1002/j.1460-2075.1996.tb00686.xopenalex-snapshot

Bacterial defense against aging: role of the Escherichia coli ArcA regulator in gene expression, readjusted energy flux and survival during stasis.

inferredcites →https://doi.org/10.1002/j.1460-2075.1996.tb00773.xopenalex-snapshot

The small RNA, DsrA, is essential for the low temperature expression of RpoS during exponential growth in Escherichia coli.

inferredcites →https://doi.org/10.1006/jmbi.1997.1310openalex-snapshot

Variation in HU composition during growth of Escherichia coli: the heterodimer is required for long term survival

inferredcites →https://doi.org/10.1006/jmbi.2000.4147openalex-snapshot

Two novel flagellar components and H-NS are involved in the motor function of Escherichia coli

inferredcites →https://doi.org/10.1007/978-0-387-78885-2_4openalex-snapshot

The Two-Component Network and the General Stress Sigma Factor RpoS (σS) in Escherichia coli

inferredcites →https://doi.org/10.1007/978-3-540-75418-3_12openalex-snapshot

Escherichia coli Biofilms

inferredcites →https://doi.org/10.1007/bf00261713openalex-snapshot

Gene fliA encodes an alternative sigma factor specific for flagellar operons in Salmonella typhimurium

inferredcites →https://doi.org/10.1007/bf00284200openalex-snapshot

Structure of the 5′ upstream region and the regulation of the rpoS gene of Escherichia coli

inferredcites →https://doi.org/10.1007/bf00331647openalex-snapshot

Pleiotropic mutations in appR reduce pH 2.5 acid phosphatase expression and restore succinate utilisation in CRP-deficient strains of Escherichia coli

inferredcites →https://doi.org/10.1007/bf02172922openalex-snapshot

Identification of cis-acting DNA sequences involved in the transcription of the virulence regulatory genespvR inSalmonella typhimurium

inferredcites →https://doi.org/10.1007/s00018-005-4557-xopenalex-snapshot

Characterization of the rdar morphotype, a multicellular behaviour in Enterobacteriaceae

inferredcites →https://doi.org/10.1007/s00203-002-0458-7openalex-snapshot

Identification of Salmonella enterica serovar Typhimurium genes associated with growth suppression in stationary-phase nutrient broth cultures and in the chicken intestine

inferredcites →https://doi.org/10.1007/s002030100277openalex-snapshot

Further studies on RpoS in enterobacteria: identification of rpoS in Enterobacter cloacae and Kluyvera cryocrescens

inferredcites →https://doi.org/10.1007/s00239-010-9352-0openalex-snapshot

Evolution of the RpoS Regulon: Origin of RpoS and the Conservation of RpoS-Dependent Regulation in Bacteria

inferredcites →https://doi.org/10.1007/s00438-004-1089-2openalex-snapshot

Microarray analysis of RpoS-mediated gene expression in Escherichia coli K-12

inferredcites →https://doi.org/10.1007/s00438-007-0311-4openalex-snapshot

RpoS regulation of gene expression during exponential growth of Escherichia coli K12

inferredcites →https://doi.org/10.1007/s00438-008-0389-3openalex-snapshot

Control of RpoS in global gene expression of Escherichia coli in minimal media

inferredcites →https://doi.org/10.1007/s004380050577openalex-snapshot

Relationships between H-NS, σS, SpvR and growth phase in the control of spvR, the regulatory gene of the Salmonella plasmid virulence operon

inferredcites →https://doi.org/10.1016/0022-2836(87)90650-4openalex-snapshot

The use of transposon TnphoA to detect genes for cell envelope proteins subject to a common regulatory stimulus

inferredcites →https://doi.org/10.1016/0022-2836(91)90366-eopenalex-snapshot

Osmotic induction of gene osmC expression in Escherichia coli K12

inferredcites →https://doi.org/10.1016/0092-8674(93)90655-aopenalex-snapshot

Survival of hunger and stress: The role of rpoS in early stationary phase gene regulation in E. coli

inferredcites →https://doi.org/10.1016/0378-1097(92)90039-qopenalex-snapshot

The putative sigma factor KatF (RpoS) is required for the transcription of the Salmonella typhimurium virulence gene spvB in Escherichia coli

inferredcites →https://doi.org/10.1016/0378-1097(94)90284-4openalex-snapshot

Role of rpoS in the regulation of Salmonella plasmid virulence (spv) genes

inferredcites →https://doi.org/10.1016/0378-1097(95)00215-qopenalex-snapshot

Regulation of hydroperoxidase (catalase) expression in Escherichia coli

inferredcites →https://doi.org/10.1016/0378-1097(95)00378-iopenalex-snapshot

Role of rpoS in the regulation of glutathione oxidoreductase ( gor) in Escherichia coli

inferredcites →https://doi.org/10.1016/0378-1119(94)90316-6openalex-snapshot

Analysis of the otsBA operon for osmoregulatory trehalose synthesis in Escherichia coli and homology of the OtsA and OtsB proteins to the yeast trehalose-6-phosphate synthase/phosphatase complex

inferredcites →https://doi.org/10.1016/j.cell.2004.05.010openalex-snapshot

Using a Quantitative Blueprint to Reprogram the Dynamics of the Flagella Gene Network

inferredcites →https://doi.org/10.1016/j.cell.2004.07.021openalex-snapshot

Regulation of RNA Polymerase through the Secondary Channel

inferredcites →https://doi.org/10.1016/j.cell.2006.04.034openalex-snapshot

rRNA Promoter Regulation by Nonoptimal Binding of σ Region 1.2: An Additional Recognition Element for RNA Polymerase

inferredcites →https://doi.org/10.1016/j.cell.2010.01.018openalex-snapshot

Second Messenger-Mediated Adjustment of Bacterial Swimming Velocity

inferredcites →https://doi.org/10.1016/j.dnarep.2010.08.004openalex-snapshot

UspB, a member of the sigma-S regulon, facilitates RuvC resolvase function

inferredcites →https://doi.org/10.1016/j.febslet.2004.11.111openalex-snapshot

Combining data from genomes, Y2H and 3D structure indicates that BolA is a reductase interacting with a glutaredoxin

inferredcites →https://doi.org/10.1016/j.febslet.2006.07.086openalex-snapshot

The membrane bound bacterial lipocalin Blc is a functional dimer with binding preference for lysophospholipids

inferredcites →https://doi.org/10.1016/j.femsle.2004.05.046openalex-snapshot

?s-Dependent regulation of yehZYXW, which encodes a putative osmoprotectant ABC transporter of Escherichia coli

inferredcites →https://doi.org/10.1016/j.femsle.2004.12.008openalex-snapshot

Role of the stress sigma factor RpoS in GacA/RsmA-controlled secondary metabolism and resistance to oxidative stress inPseudomonas fluorescensCHA0

inferredcites →https://doi.org/10.1016/j.femsle.2005.09.020openalex-snapshot

ClpXP controls the expression of LEE genes in enterohaemorrhagic Escherichia coli

inferredcites →https://doi.org/10.1016/j.femsre.2005.03.005openalex-snapshot

Salmonellastress management and its relevance to behaviour during intestinal colonisation and infection

inferredcites →https://doi.org/10.1016/j.ijmm.2006.02.017openalex-snapshot

Concert of regulators to switch on LEE expression in enterohemorrhagic Escherichia coli O157:H7: Interplay between Ler, GrlA, HNS and RpoS

inferredcites →https://doi.org/10.1016/j.jmb.2005.11.020openalex-snapshot

Structure of the Escherichia coli FlhDC Complex, a Prokaryotic Heteromeric Regulator of Transcription

inferredcites →https://doi.org/10.1016/j.jmb.2007.07.037openalex-snapshot

Structure and Function of the Escherichia coli Protein YmgB: A Protein Critical for Biofilm Formation and Acid-resistance

inferredcites →https://doi.org/10.1016/j.jmb.2007.12.037openalex-snapshot

Poising of Escherichia coli RNA Polymerase and Its Release from the σ38 C-Terminal Tail for osmY Transcription

inferredcites →https://doi.org/10.1016/j.jmb.2008.12.026openalex-snapshot

BolA Inhibits Cell Elongation and Regulates MreB Expression Levels

inferredcites →https://doi.org/10.1016/j.jmb.2010.09.038openalex-snapshot

C-Terminally Truncated Derivatives of Escherichia coli Hfq Are Proficient in Riboregulation

inferredcites →https://doi.org/10.1016/j.jphotobiol.2010.08.012openalex-snapshot

Influence of rpoS mutations on the response of Salmonella enterica serovar Typhimurium to solar radiation

inferredcites →https://doi.org/10.1016/j.jsb.2006.07.005openalex-snapshot

Coupling the distribution of RNA polymerase to global gene regulation and the dynamic structure of the bacterial nucleoid in Escherichia coli

inferredcites →https://doi.org/10.1016/j.mib.2004.02.007openalex-snapshot

Cyclic di-guanosine-monophosphate comes of age: a novel secondary messenger involved in modulating cell surface structures in bacteria?

inferredcites →https://doi.org/10.1016/j.mib.2004.02.015openalex-snapshot

Controlling mRNA stability and translation with small, noncoding RNAs

inferredcites →https://doi.org/10.1016/j.mib.2005.02.013openalex-snapshot

Sensing external stress: watchdogs of the Escherichia coli cell envelope

inferredcites →https://doi.org/10.1016/j.mib.2006.02.010openalex-snapshot

Cyclic di-GMP as a second messenger

inferredcites →https://doi.org/10.1016/j.mib.2008.02.011openalex-snapshot

New insights into transcriptional regulation by H-NS

inferredcites →https://doi.org/10.1016/j.mib.2009.01.007openalex-snapshot

Bacterial nucleotide-based second messengers

inferredcites →https://doi.org/10.1016/j.micpath.2005.11.007openalex-snapshot

Involvement of Salmonella enterica serovar Typhi RpoS in resistance to NO-mediated host defense against serovar Typhi infection

inferredcites →https://doi.org/10.1016/j.micpath.2006.01.002openalex-snapshot

Burkholderia pseudomallei RpoS regulates multinucleated giant cell formation and inducible nitric oxide synthase expression in mouse macrophage cell line (RAW 264.7)

inferredcites →https://doi.org/10.1016/j.molcel.2005.07.025openalex-snapshot

A Switch from High-Fidelity to Error-Prone DNA Double-Strand Break Repair Underlies Stress-Induced Mutation

inferredcites →https://doi.org/10.1016/j.molcel.2005.10.011openalex-snapshot

Holoenzyme Switching and Stochastic Release of Sigma Factors from RNA Polymerase In Vivo

inferredcites →https://doi.org/10.1016/j.mrfmmm.2004.04.013openalex-snapshot

Positive selection for loss of RpoS function in Escherichia coli

inferredcites →https://doi.org/10.1016/j.resmic.2004.01.014openalex-snapshot

Escherichia coli evolution during stationary phase

inferredcites →https://doi.org/10.1016/j.resmic.2004.01.020openalex-snapshot

Adaptive mutation and amplification in Escherichia coli: two pathways of genome adaptation under stress

inferredcites →https://doi.org/10.1016/j.resmic.2005.12.003openalex-snapshot

The Cpx system of Escherichia coli, a strategic signaling pathway for confronting adverse conditions and for settling biofilm communities?

inferredcites →https://doi.org/10.1016/j.resmic.2009.03.001openalex-snapshot

Cross-talk mechanisms in biofilm formation and responses to environmental and physiological stress in Escherichia coli

inferredcites →https://doi.org/10.1016/j.resmic.2009.08.006openalex-snapshot

Clp chaperone–proteases: structure and function

inferredcites →https://doi.org/10.1016/j.resmic.2009.08.014openalex-snapshot

Proteolysis of σS (RpoS) and the general stress response in Escherichia coli

inferredcites →https://doi.org/10.1016/j.resmic.2009.09.007openalex-snapshot

Proteolysis in prokaryotes – from molecular machines to a systems perspective

inferredcites →https://doi.org/10.1016/j.resmic.2009.09.016openalex-snapshot

RpoS- and Crp-dependent transcriptional control of Salmonella Typhi taiA and hlyE genes: role of environmental conditions

inferredcites →https://doi.org/10.1016/j.resmic.2010.04.002openalex-snapshot

RcsB plays a central role in H-NS-dependent regulation of motility and acid stress resistance in Escherichia coli

inferredcites →https://doi.org/10.1016/j.resmic.2010.06.009openalex-snapshot

CspC regulates rpoS transcript levels and complements hfq deletions

inferredcites →https://doi.org/10.1016/j.str.2004.01.007openalex-snapshot

Mass Spectrometry of Escherichia coli RNA Polymerase: Interactions of the Core Enzyme with σ70 and Rsd Protein

inferredcites →https://doi.org/10.1016/j.tibs.2006.10.006openalex-snapshot

ATP-dependent proteases of bacteria: recognition logic and operating principles

inferredcites →https://doi.org/10.1016/j.tig.2005.05.008openalex-snapshot

Micros for microbes: non-coding regulatory RNAs in bacteria

inferredcites →https://doi.org/10.1016/j.tim.2003.08.003openalex-snapshot

What is driving the acquisition of mutS and rpoS polymorphisms in Escherichia coli?

inferredcites →https://doi.org/10.1016/j.tim.2004.04.002openalex-snapshot

Evolutionary significance of stress-induced mutagenesis in bacteria

inferredcites →https://doi.org/10.1016/j.tim.2004.11.008openalex-snapshot

Finding gene-expression patterns in bacterial biofilms

inferredcites →https://doi.org/10.1016/j.tim.2004.11.010openalex-snapshot

Survival strategies of infectious biofilms

inferredcites →https://doi.org/10.1016/j.tim.2005.03.008openalex-snapshot

ppGpp: a global regulator in Escherichia coli

inferredcites →https://doi.org/10.1016/j.tim.2008.11.001openalex-snapshot

The developmental model of microbial biofilms: ten years of a paradigm up for review

inferredcites →https://doi.org/10.1016/j.vetmic.2008.01.008openalex-snapshot

Salmonella enterica serovar Choleraesuis derivatives harbouring deletions in rpoS and phoP regulatory genes are attenuated in pigs, and survive and multiply in porcine intestinal macrophages and fibroblasts, respectively

inferredcites →https://doi.org/10.1016/s0006-291x(02)00245-0openalex-snapshot

Cloning, sequencing, and functional studies of the rpoS gene from Vibrio harveyi

inferredcites →https://doi.org/10.1016/s0014-5793(04)00199-1openalex-snapshot

The crystal structure of the Escherichia coli lipocalin Blc suggests a possible role in phospholipid binding

inferredcites →https://doi.org/10.1016/s0021-9258(17)32210-xopenalex-snapshot

Purification and DNA-binding properties of FHLA, the transcriptional activator of the formate hydrogenlyase system from Escherichia coli.

inferredcites →https://doi.org/10.1016/s0021-9258(18)31731-9openalex-snapshot

Acetyl phosphate and the activation of two-component response regulators.

inferredcites →https://doi.org/10.1016/s0021-9258(18)86985-xopenalex-snapshot

Transcription of osmB, a gene encoding an Escherichia coli lipoprotein, is regulated by dual signals. Osmotic stress and stationary phase.

inferredcites →https://doi.org/10.1016/s0022-2836(02)01043-4openalex-snapshot

Protein–Protein and Protein–DNA Interactions of σ70 Region 4 Involved in Transcription Activation by λcI

inferredcites →https://doi.org/10.1016/s0065-2660(08)60224-2openalex-snapshot

Bacterial Genes Involved in Response to Near-Ultraviolet Radiation

inferredcites →https://doi.org/10.1016/s0065-2911(08)60133-2openalex-snapshot

The Starvation-Stress Response (SSR) of Salmonella

inferredcites →https://doi.org/10.1016/s0092-8674(00)80089-6openalex-snapshot

GASPing for Life in Stationary Phase

inferredcites →https://doi.org/10.1016/s0092-8674(00)80121-xopenalex-snapshot

Function of E. coli RNA Polymerase σ Factor- σ70 in Promoter-Proximal Pausing

inferredcites →https://doi.org/10.1016/s0092-8674(00)80312-8openalex-snapshot

A Small, Stable RNA Induced by Oxidative Stress: Role as a Pleiotropic Regulator and Antimutator

inferredcites →https://doi.org/10.1016/s0092-8674(00)80873-9openalex-snapshot

6S RNA Regulates E. coli RNA Polymerase Activity

inferredcites →https://doi.org/10.1016/s0168-1605(01)00679-1openalex-snapshot

The importance of RpoS in the survival of bacteria through food processing

inferredcites →https://doi.org/10.1016/s0168-6445(00)00031-0openalex-snapshot

The phylogeny of proteobacteria: relationships to other eubacterial phyla and eukaryotes

inferredcites →https://doi.org/10.1016/s0168-6445(03)00051-2openalex-snapshot

The MerR family of transcriptional regulators

inferredcites →https://doi.org/10.1016/s0378-1097(01)00164-1openalex-snapshot

Gene expression and protein levels of the stationary phase sigma factor, RpoS, in continuously-fed Pseudomonas aeruginosa biofilms

inferredcites →https://doi.org/10.1016/s0378-1097(02)00672-9openalex-snapshot

A mutation in rpoS enhances biofilm formation in Escherichia coli during exponential phase of growth

inferredcites →https://doi.org/10.1016/s0378-1097(99)00597-2openalex-snapshot

Effect of rpoS mutations on stress-resistance and invasion of brain microvascular endothelial cells in Escherichia coli K1

inferredcites →https://doi.org/10.1016/s0891-5849(96)00154-2openalex-snapshot

Role of escherichia coli rpos and associated genes in defense against oxidative damage

inferredcites →https://doi.org/10.1016/s0891-5849(97)00013-0openalex-snapshot

Role of RPOS Regulon in Resistance to Oxidative Stress and Near- UV Radiation In ΔOXYR Suppressor Mutants of ESCHERICHIA COLI

inferredcites →https://doi.org/10.1016/s0923-2508(00)01164-5openalex-snapshot

Survival of Escherichia coli during long-term starvation: effects of aeration, NaCl, and the rpoS and osmC gene products

inferredcites →https://doi.org/10.1016/s1097-2765(01)00436-1openalex-snapshot

Hfq

inferredcites →https://doi.org/10.1016/s1097-2765(04)00202-3openalex-snapshot

Osmo-Regulation of Bacterial Transcription via Poised RNA Polymerase

inferredcites →https://doi.org/10.1016/s1369-5274(02)00297-7openalex-snapshot

Phospholipid modifications in bacteria

inferredcites →https://doi.org/10.1016/s1369-5274(02)00372-7openalex-snapshot

Stationary phase gene regulation: what makes an Escherichia coli promoter σS-selective?

inferredcites →https://doi.org/10.1016/s1369-5274(03)00029-8openalex-snapshot

Regulation by proteolysis in bacterial cells

inferredcites →https://doi.org/10.1017/cbo9780511546242.003openalex-snapshot

Survival of environmental and host-associated stress

inferredcites →https://doi.org/10.1021/bi00092a021openalex-snapshot

In vitro functional characterization of overproduced Escherichia coli katF/rpoS gene product

inferredcites →https://doi.org/10.1021/bi800479popenalex-snapshot

Effect of Hfq on RprA−rpoS mRNA Pairing: Hfq−RNA Binding and the Influence of the 5′ rpoS mRNA Leader Region

inferredcites →https://doi.org/10.1021/bi801075xopenalex-snapshot

Remodeling and Activation of Escherichia coli RNA Polymerase by Osmolytes

inferredcites →https://doi.org/10.1021/bi961175hopenalex-snapshot

Comparative Analysis of the Interactions of Escherichia Coli σS and σ70 RNA Polymerase Holoenzyme with the Stationary-Phase-Specific bolAp1 Promoter

inferredcites →https://doi.org/10.1021/bp980102hopenalex-snapshot

Growth Rate Related Concentration Changes of the Starvation Response Regulators σS and ppGpp in Glucose-Limited Fed-Batch and Continuous Cultures of Escherichia coli

inferredcites →https://doi.org/10.1021/pr8001723openalex-snapshot

Impact of rpoS Deletion on the Proteome of Escherichia coli Grown Planktonically and as Biofilm

inferredcites →https://doi.org/10.1038/21918openalex-snapshot

DNA protection by stress-induced biocrystallization

inferredcites →https://doi.org/10.1038/219588a0openalex-snapshot

Factor Fraction required for the Synthesis of Bacteriophage Qβ-RNA

inferredcites →https://doi.org/10.1038/338652a0openalex-snapshot

Fibronectin binding mediated by a novel class of surface organelles on Escherichia coll

inferredcites →https://doi.org/10.1038/emboj.2010.179openalex-snapshot

Integrating anaerobic/aerobic sensing and the general stress response through the ArcZ small RNA

inferredcites →https://doi.org/10.1038/emboj.2010.36openalex-snapshot

Daughter cell separation is controlled by cytokinetic ring‐activated cell wall hydrolysis

inferredcites →https://doi.org/10.1038/ismej.2008.24openalex-snapshot

Escherichia coli transcription factor YncC (McbR) regulates colanic acid and biofilm formation by repressing expression of periplasmic protein YbiM (McbA)

inferredcites →https://doi.org/10.1038/ismej.2008.4openalex-snapshot

Evolutionary loss of the rdar morphotype in Salmonella as a result of high mutation rates during laboratory passage

inferredcites →https://doi.org/10.1038/nature752openalex-snapshot

Crystal structure of a bacterial RNA polymerase holoenzyme at 2.6 Å resolution

inferredcites →https://doi.org/10.1038/ng881openalex-snapshot

Network motifs in the transcriptional regulation network of Escherichia coli

inferredcites →https://doi.org/10.1038/nrmicro1021openalex-snapshot

Escherichia coli acid resistance: tales of an amateur acidophile

inferredcites →https://doi.org/10.1038/nrmicro1340openalex-snapshot

Long-term survival during stationary phase: evolution and the GASP phenotype

inferredcites →https://doi.org/10.1038/nrmicro1887openalex-snapshot

Coordinating assembly of a bacterial macromolecular machine

inferredcites →https://doi.org/10.1038/nrmicro2109openalex-snapshot

Principles of c-di-GMP signalling in bacteria

inferredcites →https://doi.org/10.1038/nrmicro818openalex-snapshot

Pathogenic Escherichia coli

inferredcites →https://doi.org/10.1038/nrmicro883openalex-snapshot

H-NS: a universal regulator for a dynamic genome

inferredcites →https://doi.org/10.1038/nsb0498-294openalex-snapshot

The crystal structure of Dps, a ferritin homolog that binds and protects DNA

inferredcites →https://doi.org/10.1038/nsmb.1380openalex-snapshot

Protein unfolding by a AAA+ protease is dependent on ATP-hydrolysis rates and substrate energy landscapes

inferredcites →https://doi.org/10.1038/nsmb1130openalex-snapshot

Extensive functional overlap between σ factors in Escherichia coli

inferredcites →https://doi.org/10.1038/nsmb768openalex-snapshot

The σ70 subunit of RNA polymerase induces lacUV5 promoter-proximal pausing of transcription

inferredcites →https://doi.org/10.1038/nsmb858openalex-snapshot

Escherichia coli Hfq has distinct interaction surfaces for DsrA, rpoS and poly(A) RNAs

inferredcites →https://doi.org/10.1038/sj.emboj.7601041openalex-snapshot

Potassium glutamate as a transcriptional inhibitor during bacterial osmoregulation

inferredcites →https://doi.org/10.1038/sj.emboj.7601629openalex-snapshot

Stationary phase reorganisation of the Escherichia coli transcription machinery by Crl protein, a fine‐tuner of σs activity and levels

inferredcites →https://doi.org/10.1038/sj.embor.7400729openalex-snapshot

Homeostatic regulation of supercoiling sensitivity coordinates transcription of the bacterial genome

inferredcites →https://doi.org/10.1038/sj.embor.embor733openalex-snapshot

Growth‐rate dependent RNA polyadenylation in Escherichia coli

inferredcites →https://doi.org/10.1038/sj.hdy.6801077openalex-snapshot

The spread of a beneficial mutation in experimental bacterial populations: the influence of the environment and genotype on the fixation of rpoS mutations

inferredcites →https://doi.org/10.1039/b904955jopenalex-snapshot

A global view of Escherichia coli Rsd protein and its interactions

inferredcites →https://doi.org/10.1046/j.1365-2958.1996.00058.xopenalex-snapshot

Identification of σs‐dependent genes associated with the stationary‐phase acid‐resistance phenotype of Shigella flexneri

inferredcites →https://doi.org/10.1046/j.1365-2958.1996.418945.xopenalex-snapshot

Growth‐phase‐dependent expression of the osmotically inducible gene osmC of Escherichia coli K‐12

inferredcites →https://doi.org/10.1046/j.1365-2958.1996.511405.xopenalex-snapshot

Back to log phase: σS as a global regulator in the osmotic control of gene expression in Escherichia coli

inferredcites →https://doi.org/10.1046/j.1365-2958.1997.3961742.xopenalex-snapshot

The σS level in starving Escherichia coli cells increases solely as a result of its increased stability, despite decreased synthesis

inferredcites →https://doi.org/10.1046/j.1365-2958.1997.4911852.xopenalex-snapshot

The LysR‐like regulator LeuO in Escherichia coli is involved in the translational regulation of rpoS by affecting the expression of the small regulatory DsrA‐RNA

inferredcites →https://doi.org/10.1046/j.1365-2958.1998.00725.xopenalex-snapshot

Regulation of RssB‐dependent proteolysis in Escherichia coli: a role for acetyl phosphate in a response regulator‐controlled process

inferredcites →https://doi.org/10.1046/j.1365-2958.1998.00791.xopenalex-snapshot

Multicellular and aggregative behaviour of Salmonella typhimurium strains is controlled by mutations in the agfD promoter

inferredcites →https://doi.org/10.1046/j.1365-2958.1998.00855.xopenalex-snapshot

Interplay between global regulators of Escherichia coli : effect of RpoS, Lrp and H‐NS on transcription of the gene osmC

inferredcites →https://doi.org/10.1046/j.1365-2958.1998.00990.xopenalex-snapshot

Negative regulation by RpoS: a case of sigma factor competition

inferredcites →https://doi.org/10.1046/j.1365-2958.1998.01007.xopenalex-snapshot

Crl stimulates RpoS activity during stationary phase

inferredcites →https://doi.org/10.1046/j.1365-2958.1998.01077.xopenalex-snapshot

The ftsQ1p gearbox promoter of Escherichia coli is a major sigma S‐dependent promoter in the ddlB – ftsA region

inferredcites →https://doi.org/10.1046/j.1365-2958.1999.01343.xopenalex-snapshot

The regulation and role of the periplasmic copper, zinc superoxide dismutase of Escherichia coli

inferredcites →https://doi.org/10.1046/j.1365-2958.1999.01397.xopenalex-snapshot

The stationary‐phase morphogene bolA from Escherichia coli is induced by stress during early stages of growth

inferredcites →https://doi.org/10.1046/j.1365-2958.1999.01456.xopenalex-snapshot

Membrane cyclopropane fatty acid content is a major factor in acid resistance of Escherichia coli

inferredcites →https://doi.org/10.1046/j.1365-2958.2000.01736.xopenalex-snapshot

The response regulator RssB, a recognition factor for σS proteolysis in Escherichia coli, can act like an anti‐σS factor

inferredcites →https://doi.org/10.1046/j.1365-2958.2000.01758.xopenalex-snapshot

Involvement of differential efficiency of transcription by Eσs and Eσ70 RNA polymerase holoenzymes in growth phase regulation of the Escherichia coli osmE promoter

inferredcites →https://doi.org/10.1046/j.1365-2958.2000.01822.xopenalex-snapshot

AgfD, the checkpoint of multicellular and aggregative behaviour in Salmonella typhimurium regulates at least two independent pathways

inferredcites →https://doi.org/10.1046/j.1365-2958.2000.01972.xopenalex-snapshot

UPs and downs in bacterial transcription initiation: the role of the alpha subunit of RNA polymerase in promoter recognition

inferredcites →https://doi.org/10.1046/j.1365-2958.2000.01999.xopenalex-snapshot

Transcriptional induction of the conserved alternative sigma factor RpoS in Escherichia coli is dependent on BarA, a probable two‐component regulator

inferredcites →https://doi.org/10.1046/j.1365-2958.2000.02162.xopenalex-snapshot

Riboregulation by DsrA RNA: trans‐actions for global economy

inferredcites →https://doi.org/10.1046/j.1365-2958.2001.02305.xopenalex-snapshot

The Escherichia coli histone‐like protein HU regulates rpoS translation

inferredcites →https://doi.org/10.1046/j.1365-2958.2001.02313.xopenalex-snapshot

What makes an Escherichia coli promoter sigmaS dependent? Role of the -13/-14 nucleotide promoter positions and region 2.5 of sigmaS

inferredcites →https://doi.org/10.1046/j.1365-2958.2001.02329.xopenalex-snapshot

Regulation of RpoS by a novel small RNA: the characterization of RprA

inferredcites →https://doi.org/10.1046/j.1365-2958.2001.02337.xopenalex-snapshot

The multicellular morphotypes of Salmonella typhimurium and Escherichia coli produce cellulose as the second component of the extracellular matrix

inferredcites →https://doi.org/10.1046/j.1365-2958.2001.02465.xopenalex-snapshot

RpoS co‐operates with other factors to induce Legionella pneumophila virulence in the stationary phase

inferredcites →https://doi.org/10.1046/j.1365-2958.2001.02482.xopenalex-snapshot

Role of the response regulator RssB in σS recognition and initiation of σS proteolysis in Escherichia coli

inferredcites →https://doi.org/10.1046/j.1365-2958.2001.02529.xopenalex-snapshot

MlrA, a novel regulator of curli (AgF) and extracellular matrix synthesis by Escherichia coli and Salmonella enterica serovar Typhimurium

inferredcites →https://doi.org/10.1046/j.1365-2958.2001.02548.xopenalex-snapshot

Role of activator site position and a distal UP‐element half‐site for sigma factor selectivity at a CRP/H‐NS‐activated σS‐dependent promoter in Escherichia coli

inferredcites →https://doi.org/10.1046/j.1365-2958.2001.02559.xopenalex-snapshot

Escherichia coli DNA glycosylase Mug: a growth‐regulated enzyme required for mutation avoidance in stationary‐phase cells

inferredcites →https://doi.org/10.1046/j.1365-2958.2001.02570.xopenalex-snapshot

An activator of glutamate decarboxylase genes regulates the expression of enteropathogenic Escherichia coli virulence genes through control of the plasmid‐encoded regulator, Per

inferredcites →https://doi.org/10.1046/j.1365-2958.2001.02703.xopenalex-snapshot

Promoter recognition and discrimination by Eσ S RNA polymerase

inferredcites →https://doi.org/10.1046/j.1365-2958.2002.03123.xopenalex-snapshot

The cellular level of the recognition factor RssB is rate‐limiting for σS proteolysis: implications for RssB regulation and signal transduction in σS turnover in Escherichia coli

inferredcites →https://doi.org/10.1046/j.1365-2958.2002.03131.xopenalex-snapshot

The gene bolA regulates dacA (PBP5), dacC (PBP6) and ampC (AmpC), promoting normal morphology in Escherichia coli

inferredcites →https://doi.org/10.1046/j.1365-2958.2002.03203.xopenalex-snapshot

Regulation and mode of action of the second small RNA activator of RpoS translation, RprA

inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03432.xopenalex-snapshot

Global gene expression in Escherichia coli biofilms

inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03437.xopenalex-snapshot

Turnover of FlhD and FlhC, master regulator proteins for Salmonella flagellum biogenesis, by the ATP‐dependent ClpXP protease

inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03454.xopenalex-snapshot

Small non‐coding RNAs, co‐ordinators of adaptation processes in Escherichia coli: the RpoS paradigm

inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03461.xopenalex-snapshot

DNA supercoiling contributes to disconnect σS accumulation from σS‐dependent transcription in Escherichia coli

inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03477.xopenalex-snapshot

Regulatory network of acid resistance genes in Escherichia coli

inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03633.xopenalex-snapshot

GadE (YhiE) activates glutamate decarboxylase‐dependent acid resistance in Escherichia coli K‐12

inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03644.xopenalex-snapshot

Dynamic control of Dps protein levels by ClpXP and ClpAP proteases in Escherichia coli

inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03704.xopenalex-snapshot

Error‐prone DNA polymerase IV is controlled by the stress‐response sigma factor, RpoS, in Escherichia coli

inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03734.xopenalex-snapshot

Global analysis of small RNA and mRNA targets of Hfq

inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03865.xopenalex-snapshot

Global impact of mature biofilm lifestyle on Escherichia coli K‐12 gene expression

inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03867.xopenalex-snapshot

Multiple stress signal integration in the regulation of the complex σS‐dependent csiD‐ygaF‐gabDTP operon in Escherichia coli

inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03886.xopenalex-snapshot

The Pseudomonas aeruginosa RpoS regulon and its relationship to quorum sensing

inferredcites →https://doi.org/10.1046/j.1462-2920.2000.00128.xopenalex-snapshot

Developmental pathway for biofilm formation in curli‐producing Escherichia coli strains: role of flagella, curli and colanic acid

inferredcites →https://doi.org/10.1046/j.1462-2920.2001.00238.xopenalex-snapshot

Hungry bacteria – definition and properties of a nutritional state

inferredcites →https://doi.org/10.1073/pnas.0403064101openalex-snapshot

Identification of a quinone-sensitive redox switch in the ArcB sensor kinase

inferredcites →https://doi.org/10.1073/pnas.042521699openalex-snapshot

Surface sensing and adhesion of Escherichia coli controlled by the Cpx-signaling pathway

inferredcites →https://doi.org/10.1073/pnas.0502890102openalex-snapshot

Quorum sensing and multidrug transporters in Escherichia coli

inferredcites →https://doi.org/10.1073/pnas.0510995103openalex-snapshot

Guanosine 3′,5′-bispyrophosphate coordinates global gene expression during glucose-lactose diauxie in Escherichia coli

inferredcites →https://doi.org/10.1073/pnas.0600828103openalex-snapshot

Insights into transcriptional regulation and σ competition from an equilibrium model of RNA polymerase binding to DNA

inferredcites →https://doi.org/10.1073/pnas.0606026103openalex-snapshot

The PhoP/PhoQ two-component system stabilizes the alternative sigma factor RpoS in Salmonella enterica

inferredcites →https://doi.org/10.1073/pnas.0803665106openalex-snapshot

A DNA damage response in Escherichia coli involving the alternative sigma factor, RpoS

inferredcites →https://doi.org/10.1073/pnas.1004435107openalex-snapshot

Positive regulation by small RNAs and the role of Hfq

inferredcites →https://doi.org/10.1073/pnas.170281497openalex-snapshot

A trans-acting RNA as a control switch in Escherichia coli : DsrA modulates function by forming alternative structures

inferredcites →https://doi.org/10.1073/pnas.212510999openalex-snapshot

Adaptation to famine: A family of stationary-phase genes revealed by microarray analysis

inferredcites →https://doi.org/10.1073/pnas.2536607100openalex-snapshot

A role for mechanosensitive channels in survival of stationary phase: Regulation of channel expression by RpoS

inferredcites →https://doi.org/10.1073/pnas.86.9.3271openalex-snapshot

Exonuclease III and the catalase hydroperoxidase II in Escherichia coli are both regulated by the katF gene product.

inferredcites →https://doi.org/10.1073/pnas.89.24.11978openalex-snapshot

The alternative sigma factor katF (rpoS) regulates Salmonella virulence.

showing the first 200 of 541 · page through all 541

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