review article | Q7318358 |
scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1047089157 |
P356 | DOI | 10.1038/NRMICRO.2016.107 |
P698 | PubMed publication ID | 27510862 |
P2093 | author name string | Dianne K Newman | |
Megan Bergkessel | |||
David W Basta | |||
P2860 | cites work | RsfA (YbeB) proteins are conserved ribosomal silencing factors | Q21092415 |
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Dps protects cells against multiple stresses during stationary phase | Q24564681 | ||
Energetics of syntrophic cooperation in methanogenic degradation | Q24643733 | ||
Pseudomonas aeruginosa mutants affected in anaerobic growth on arginine: evidence for a four-gene cluster encoding the arginine deiminase pathway | Q24683064 | ||
Life under extreme energy limitation: a synthesis of laboratory- and field-based investigations | Q26828792 | ||
Metabolic co-dependence gives rise to collective oscillations within biofilms. | Q27316145 | ||
Live-cell superresolution microscopy reveals the organization of RNA polymerase in the bacterial nucleoid | Q27322413 | ||
A NusE:NusG complex links transcription and translation | Q27660765 | ||
Structure and function of CarD, an essential mycobacterial transcription factor | Q27679098 | ||
The crystal structure of Dps, a ferritin homolog that binds and protects DNA | Q27749085 | ||
(p)ppGpp: still magical? | Q28278758 | ||
CarD is an essential regulator of rRNA transcription required for Mycobacterium tuberculosis persistence | Q28486907 | ||
The Mycobacterium tuberculosis DosR regulon assists in metabolic homeostasis and enables rapid recovery from nonrespiring dormancy | Q28487516 | ||
RpoS proteolysis is controlled directly by ATP levels in Escherichia coli | Q42053587 | ||
A genetically encoded fluorescent reporter of ATP:ADP ratio | Q43190761 | ||
Multidimensional optimality of microbial metabolism | Q43431493 | ||
Control of rRNA expression by small molecules is dynamic and nonredundant | Q44530417 | ||
How Geobacteraceae may dominate subsurface biodegradation: physiology of Geobacter metallireducens in slow-growth habitat-simulating retentostats. | Q45917566 | ||
Selective repression by Fis and H-NS at the Escherichia coli dps promoter. | Q46386594 | ||
Unveiling the Metabolic Pathways Associated with the Adaptive Reduction of Cell Size During Vibrio harveyi Persistence in Seawater Microcosms | Q46738728 | ||
Maintenance energy requirement: what is required for stasis survival of Escherichia coli? | Q47729504 | ||
BONCAT: metabolic labeling, click chemistry, and affinity purification of newly synthesized proteomes | Q48390741 | ||
Synthesis-mediated release of a small RNA inhibitor of RNA polymerase. | Q54450635 | ||
Bacterial nucleoid dynamics: oxidative stress response in Staphylococcus aureus. | Q54467053 | ||
Competition, Not Cooperation, Dominates Interactions among Culturable Microbial Species | Q57197359 | ||
Regulation through the Secondary Channel—Structural Framework for ppGpp-DksA Synergism during Transcription | Q57895265 | ||
Metabolite-based mutualism between Pseudomonas aeruginosa PA14 and Enterobacter aerogenes enhances current generation in bioelectrochemical systems | Q61942144 | ||
Nucleoid restructuring in stationary-state bacteria | Q63761948 | ||
Purification and properties of the Escherichia coli host factor required for inversion of the G segment in bacteriophage Mu | Q68917141 | ||
Gene expression profile of Vibrio cholerae in the cold stress-induced viable but non-culturable state | Q79946965 | ||
DksA: a critical component of the transcription initiation machinery that potentiates the regulation of rRNA promoters by ppGpp and the initiating NTP | Q80417641 | ||
Survival and viability of nonculturableEscherichia coli andVibrio cholerae in the estuarine and marine environment | Q86719054 | ||
Microbial persistence and the road to drug resistance | Q38114534 | ||
The phenomenon of microbial uncultivability | Q38134984 | ||
A paradigm for endosymbiotic life: cell differentiation of Rhizobium bacteria provoked by host plant factors. | Q38136269 | ||
Long-term anaerobic survival of the opportunistic pathogen Pseudomonas aeruginosa via pyruvate fermentation | Q38339381 | ||
Regulation of Transcript Elongation | Q38541517 | ||
Growth in studying the cessation of growth. | Q39493943 | ||
DksA guards elongating RNA polymerase against ribosome-stalling-induced arrest | Q39688530 | ||
A two-component phosphotransfer network involving ArcB, ArcA, and RssB coordinates synthesis and proteolysis of sigmaS (RpoS) in E. coli | Q39705576 | ||
Microbial physiology and ecology of slow growth. | Q40024277 | ||
The growth advantage in stationary-phase phenotype conferred by rpoS mutations is dependent on the pH and nutrient environment | Q40345503 | ||
Fundamental structural units of the Escherichia coli nucleoid revealed by atomic force microscopy | Q40773408 | ||
Dynamic exometabolome analysis reveals active metabolic pathways in non-replicating mycobacteria. | Q40997810 | ||
Bridging the gap between viable but non-culturable and antibiotic persistent bacteria | Q41634417 | ||
An integrated approach reveals regulatory controls on bacterial translation elongation | Q41900904 | ||
Transcription factor GreA contributes to resolving promoter-proximal pausing of RNA polymerase in Bacillus subtilis cells | Q41902114 | ||
DksA represses ribosomal gene transcription in Pseudomonas aeruginosa by interacting with RNA polymerase on ribosomal promoters | Q28493101 | ||
A moonlighting enzyme links Escherichia coli cell size with central metabolism | Q28534852 | ||
On the evolution of bacterial multicellularity | Q28650712 | ||
Nonreplicating persistence of mycobacterium tuberculosis | Q29615312 | ||
Bacterial persistence as a phenotypic switch | Q29618111 | ||
Regulation of phenotypic variability by a threshold-based mechanism underlies bacterial persistence | Q30495567 | ||
Fumarate reductase activity maintains an energized membrane in anaerobic Mycobacterium tuberculosis. | Q31036537 | ||
Organization of ribosomes and nucleoids in Escherichia coli cells during growth and in quiescence | Q31153623 | ||
Raman-FISH: combining stable-isotope Raman spectroscopy and fluorescence in situ hybridization for the single cell analysis of identity and function. | Q33291043 | ||
Heterogeneous rpoS and rhlR mRNA levels and 16S rRNA/rDNA (rRNA gene) ratios within Pseudomonas aeruginosa biofilms, sampled by laser capture microdissection | Q33546954 | ||
Control of rRNA synthesis in Escherichia coli: a systems biology approach | Q33559589 | ||
Prolonged stationary-phase incubation selects for lrp mutations in Escherichia coli K-12 | Q33603147 | ||
Phenazine redox cycling enhances anaerobic survival in Pseudomonas aeruginosa by facilitating generation of ATP and a proton-motive force | Q33716449 | ||
Genome-Wide Translational Profiling by Ribosome Footprinting | Q33718812 | ||
DNA protection by stress-induced biocrystallization | Q33867772 | ||
Metabolism, cell growth and the bacterial cell cycle. | Q33919683 | ||
A pause sequence enriched at translation start sites drives transcription dynamics in vivo | Q33939698 | ||
Current Perspectives on Viable but Non-Culturable (VBNC) Pathogenic Bacteria | Q33978716 | ||
Mutations enhancing amino acid catabolism confer a growth advantage in stationary phase | Q33992996 | ||
Capture of arginine at low concentrations by a marine psychrophilic bacterium | Q34029967 | ||
The RpoS-mediated general stress response in Escherichia coli | Q34189650 | ||
Methanobacillus omelianskii, a symbiotic association of two species of bacteria | Q34236398 | ||
Microbial Competition: Escherichia coli Mutants That Take Over Stationary Phase Cultures | Q34305902 | ||
Sulfonate-sulfur metabolism and its regulation in Escherichia coli | Q34323107 | ||
Transposon insertion sequencing: a new tool for systems-level analysis of microorganisms. | Q34347048 | ||
DNA condensation and self-aggregation of Escherichia coli Dps are coupled phenomena related to the properties of the N-terminus | Q34366346 | ||
rpoS mutations and loss of general stress resistance in Escherichia coli populations as a consequence of conflict between competing stress responses | Q34434398 | ||
The DNA-Binding Protein from Starved Cells (Dps) Utilizes Dual Functions To Defend Cells against Multiple Stresses. | Q34487183 | ||
The bacterial translation stress response. | Q34490409 | ||
Growth phase-dependent regulation and stringent control of fis are conserved processes in enteric bacteria and involve a single promoter (fis P) in Escherichia coli | Q34555728 | ||
The Listeria monocytogenes hibernation-promoting factor is required for the formation of 100S ribosomes, optimal fitness, and pathogenesis | Q34853421 | ||
HipA-mediated antibiotic persistence via phosphorylation of the glutamyl-tRNA-synthetase | Q35068644 | ||
The phosphate starvation stimulon of Corynebacterium glutamicum determined by DNA microarray analyses | Q35162224 | ||
Stable-isotope probing of nucleic acids: a window to the function of uncultured microorganisms | Q35172620 | ||
Degradation of stable RNA in bacteria | Q35207031 | ||
Stress sigma factor RpoS degradation and translation are sensitive to the state of central metabolism | Q35549117 | ||
Role of the Escherichia coli FadR regulator in stasis survival and growth phase-dependent expression of the uspA, fad, and fab genes | Q35616465 | ||
Effects of nutrition and growth rate on Lrp levels in Escherichia coli | Q35617590 | ||
Nitrogen regulatory protein C-controlled genes of Escherichia coli: scavenging as a defense against nitrogen limitation | Q35852947 | ||
Heterogeneity in Pseudomonas aeruginosa biofilms includes expression of ribosome hibernation factors in the antibiotic-tolerant subpopulation and hypoxia-induced stress response in the metabolically active population | Q35867693 | ||
Stationary-phase physiology | Q35919834 | ||
Pediatric Cystic Fibrosis Sputum Can Be Chemically Dynamic, Anoxic, and Extremely Reduced Due to Hydrogen Sulfide Formation | Q36002677 | ||
Defining bacterial regulons using ChIP-seq | Q36079824 | ||
Regional Isolation Drives Bacterial Diversification within Cystic Fibrosis Lungs | Q36109214 | ||
Linking microbial community structure with function: fluorescence in situ hybridization-microautoradiography and isotope arrays | Q36353132 | ||
Roles of Nucleoid-Associated Proteins in Stress-Induced Mutagenic Break Repair in Starving Escherichia coli | Q36365259 | ||
Regulation of Bacterial DNA Packaging in Early Stationary Phase by Competitive DNA Binding of Dps and IHF | Q36367267 | ||
Long-term survival during stationary phase: evolution and the GASP phenotype | Q36369839 | ||
Evolution of microbial diversity during prolonged starvation | Q36456226 | ||
Trace incorporation of heavy water reveals slow and heterogeneous pathogen growth rates in cystic fibrosis sputum | Q36483152 | ||
SutA is a bacterial transcription factor expressed during slow growth in Pseudomonas aeruginosa | Q36563139 | ||
Effect of nutrient deprivation on lipid, carbohydrate, DNA, RNA, and protein levels in Vibrio cholerae | Q36667590 | ||
Starvation-survival patterns of sixteen freshly isolated open-ocean bacteria. | Q36713457 | ||
High-Throughput Single-Cell Cultivation on Microfluidic Streak Plates | Q36728085 | ||
The molecular basis of selective promoter activation by the sigmaS subunit of RNA polymerase. | Q36736448 | ||
Adenylate energy charge in Escherichia coli during growth and starvation | Q36774259 | ||
Multifunctional essentiality of succinate metabolism in adaptation to hypoxia in Mycobacterium tuberculosis | Q36782015 | ||
Divergent protein motifs direct elongation factor P-mediated translational regulation in Salmonella enterica and Escherichia coli | Q36800967 | ||
Competitive fitness during feast and famine: how SOS DNA polymerases influence physiology and evolution in Escherichia coli | Q36878608 | ||
The protonmotive force is required for maintaining ATP homeostasis and viability of hypoxic, nonreplicating Mycobacterium tuberculosis | Q36954404 | ||
Initiation of ribosome degradation during starvation in Escherichia coli | Q37168958 | ||
Redox-sensitive green fluorescent protein: probes for dynamic intracellular redox responses. A review | Q37373607 | ||
Direct observation of single stationary-phase bacteria reveals a surprisingly long period of constant protein production activity | Q37474918 | ||
RIPiT-Seq: a high-throughput approach for footprinting RNA:protein complexes. | Q37619861 | ||
Bacterial nucleoid-associated proteins, nucleoid structure and gene expression | Q37688895 | ||
Studying bacterial transcriptomes using RNA-seq | Q37796158 | ||
Recent progress in Bacillus subtilis sporulation | Q37957161 | ||
Regulating DNA replication in bacteria | Q38087526 | ||
P433 | issue | 9 | |
P407 | language of work or name | English | Q1860 |
P1104 | number of pages | 14 | |
P304 | page(s) | 549-562 | |
P577 | publication date | 2016-08-01 | |
P1433 | published in | Nature Reviews Microbiology | Q1071797 |
P1476 | title | The physiology of growth arrest: uniting molecular and environmental microbiology | |
P478 | volume | 14 |
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