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Condition-Dependent Resource Allocation Strategy Governed by Cody Regulator In Bacillus subtilis

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INDUCED BIOCHEMICAL MUTATIONS IN BACILLUS SUBTILIS
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Fundamental limits on the rate of bacterial growth and their influence on proteomic composition
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CodY, a global regulator of stationary phase and virulence in Gram-positive bacteria
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Coupling of Ribosome Synthesis and Translational Capacity with Cell Growth
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Plasmids for ectopic integration in Bacillus subtilis
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Coordination of bacterial proteome with metabolism by cyclic AMP signalling
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Overflow metabolism in Escherichia coli results from efficient proteome allocation
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The MaxQuant computational platform for mass spectrometry-based shotgun proteomics
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Feast and famine — microbial life in the deep-sea bed
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Control of key metabolic intersections in Bacillus subtilis
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The protein translation machinery is expressed for maximal efficiency in Escherichia coli
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Stringent response ensures the timely adaptation of bacterial growth to nutrient downshift
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An integrative circuit–host modelling framework for predicting synthetic gene network behaviours
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General quantitative relations linking cell growth and the cell cycle in Escherichia coli
inferredcites →https://doi.org/10.1038/s41564-022-01310-wopenalex-extracted
Enzyme expression kinetics by Escherichia coli during transition from rich to minimal media depends on proteome reserves
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The gut microbiome in feast and famine
inferredcites →https://doi.org/10.1038/s41579-021-00626-4openalex-extracted
Bacterial motility: machinery and mechanisms
inferredcites →https://doi.org/10.1038/s41579-022-00818-6openalex-extracted
Shaping bacterial gene expression by physiological and proteome allocation constraints
inferredcites →https://doi.org/10.1038/s41586-020-2505-4openalex-extracted
A universal trade-off between growth and lag in fluctuating environments
inferredcites →https://doi.org/10.1038/s41586-020-2638-5openalex-extracted
Functionally uncoupled transcription–translation in Bacillus subtilis
inferredcites →https://doi.org/10.1038/s41588-017-0012-9openalex-extracted
Genomic features of bacterial adaptation to plants
inferredcites →https://doi.org/10.1038/s41589-023-01302-9openalex-extracted
Unbalanced response to growth variations reshapes the cell fate decision landscape
inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03818.xopenalex-extracted
The Spo0A regulon of Bacillus subtilis
inferredcites →https://doi.org/10.1073/pnas.1300428110openalex-extracted
Genome-wide identification of Bacillus subtilis CodY-binding sites at single-nucleotide resolution
inferredcites →https://doi.org/10.1073/pnas.1314810111openalex-extracted
Visual account of protein investment in cellular functions
inferredcites →https://doi.org/10.1073/pnas.1321308111openalex-extracted
Hierarchical expression of genes controlled by the Bacillus subtilis global regulatory protein CodY
inferredcites →https://doi.org/10.1073/pnas.2201585119openalex-extracted
Cellular perception of growth rate and the mechanistic origin of bacterial growth law
inferredcites →https://doi.org/10.1074/jbc.m116.754309openalex-extracted
Structure of the Branched-chain Amino Acid and GTP-sensing Global Regulator, CodY, from Bacillus subtilis
inferredcites →https://doi.org/10.1074/mcp.tir118.000900openalex-extracted
Online Parallel Accumulation–Serial Fragmentation (PASEF) with a Novel Trapped Ion Mobility Mass Spectrometer
inferredcites →https://doi.org/10.1093/femsre/fuab038openalex-extracted
Multiple functions of flagellar motility and chemotaxis in bacterial physiology
inferredcites →https://doi.org/10.1093/nar/gkab943openalex-extracted
The current state of Subti Wiki, the database for the model organism Bacillus subtilis
inferredcites →https://doi.org/10.1103/physrevlett.125.028103openalex-extracted
Ribosome Composition Maximizes Cellular Growth Rates in E. coli
inferredcites →https://doi.org/10.1111/febs.13258openalex-extracted
How fast‐growing bacteria robustly tune their ribosome concentration to approximate growth‐rate maximization
inferredcites →https://doi.org/10.1111/j.1574-6976.2011.00310.xopenalex-extracted
Recent progress in Bacillus subtilis sporulation
inferredcites →https://doi.org/10.1126/science.1192588openalex-extracted
Interdependence of Cell Growth and Gene Expression: Origins and Consequences
inferredcites →https://doi.org/10.1128/ecosal.8.3.1.2openalex-extracted
The Life of CommensalEscherichia coliin the Mammalian Intestine
inferredcites →https://doi.org/10.1128/ecosalplus.5.6.3openalex-extracted
Stationary-Phase Gene Regulation in Escherichia coli §
inferredcites →https://doi.org/10.1128/jb.00818-09openalex-extracted
Genetic and Biochemical Analysis of the Interaction ofBacillus subtilisCodY with Branched-Chain Amino Acids
inferredcites →https://doi.org/10.1128/jb.00937-10openalex-extracted
Regulation of CodY Activity through Modulation of Intracellular Branched-Chain Amino Acid Pools
inferredcites →https://doi.org/10.1128/jb.01115-07openalex-extracted
Interaction ofBacillus subtilisCodY with GTP
inferredcites →https://doi.org/10.1128/jb.183.14.4393-4393.2001openalex-extracted
Development of a New Integration Site within the Bacillus subtilis Chromosome and Construction of Compatible Expression Cassettes
inferredcites →https://doi.org/10.1128/mbio.02205-19openalex-extracted
Control of Bacillus subtilis Replication Initiation during Physiological Transitions and Perturbations
inferredcites →https://doi.org/10.1146/annurev-micro-090110-102946openalex-extracted
The RpoS-Mediated General Stress Response in Escherichia coli
inferredcites →https://doi.org/10.1146/annurev.arplant.57.032905.105159openalex-extracted
THE ROLE OF ROOT EXUDATES IN RHIZOSPHERE INTERACTIONS WITH PLANTS AND OTHER ORGANISMS
inferredcites →https://doi.org/10.1146/annurev.micro.61.080706.093445openalex-extracted
SigB-Dependent General Stress Response in Bacillus subtilis and Related Gram-Positive Bacteria
inferredcites →https://doi.org/10.15252/msb.20145379openalex-extracted
Emergence of robust growth laws from optimal regulation of ribosome synthesis
inferredcites →https://doi.org/10.15252/msb.20209478openalex-extracted
Slower growth of Escherichia coli leads to longer survival in carbon starvation due to a decrease in the maintenance rate
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