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Control of key metabolic intersections in Bacillus subtilis

https://doi.org/10.1038/nrmicro1772
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1006/jmbi.1998.2492openalex-snapshot
Phosphorylation of either Crh or HPr mediates binding of CcpA to the Bacillus subtilis xyn cre and catabolite repression of the xyn operon 1 1Edited by I. B. Holland
inferredcites →https://doi.org/10.1006/jmbi.1999.3420openalex-snapshot
CcpC, a novel regulator of the LysR family required for glucose repression of the citB gene in Bacillus subtilis
inferredcites →https://doi.org/10.1007/s00203-005-0078-0openalex-snapshot
Regulation of citB expression in Bacillus subtilis: integration of multiple metabolic signals in the citrate pool and by the general nitrogen regulatory system
inferredcites →https://doi.org/10.1016/0022-2836(70)90144-0openalex-snapshot
lac repressor—Operator interaction
inferredcites →https://doi.org/10.1016/0022-2836(72)90253-7openalex-snapshot
lac repressor-operator interaction
inferredcites →https://doi.org/10.1016/0022-2836(87)90204-xopenalex-snapshot
Catabolite repression-resistant mutations of the Bacillus subtilis alpha-amylase promoter affect transcription levels and are in an operator-like sequence
inferredcites →https://doi.org/10.1016/0022-2836(89)90290-8openalex-snapshot
Regulation of Bacillus subtilis glutamine synthetase gene expression by the product of the glnR gene
inferredcites →https://doi.org/10.1016/0300-9084(88)90119-8openalex-snapshot
Escherichia coli and Salmonella typhimurium: Cellular and molecular biology
inferredcites →https://doi.org/10.1016/0378-1119(88)90042-xopenalex-snapshot
Sequence of the Bacillus subtilis glutamine synthetase gene region
inferredcites →https://doi.org/10.1016/j.femsre.2004.11.002openalex-snapshot
The PEP—pyruvate—oxaloacetate node as the switch point for carbon flux distribution in bacteria: We dedicate this paper to Rudolf K. Thauer, Director of the Max-Planck-Institute for Terrestrial Microbiology in Marburg, Germany, on the occasion of his 65th birthday
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Linking the nutritional status of Streptococcus pyogenes to alteration of transcriptional gene expression: The action of CodY and RelA
inferredcites →https://doi.org/10.1016/j.jmb.2006.10.100openalex-snapshot
Molecular Mechanism of the Regulation of Bacillus subtilis gltAB Expression by GltC
inferredcites →https://doi.org/10.1016/j.jmb.2007.02.054openalex-snapshot
Structural Mechanism for the Fine-tuning of CcpA Function by The Small Molecule Effectors Glucose 6-Phosphate and Fructose 1,6-Bisphosphate
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CodY, a global regulator of stationary phase and virulence in Gram-positive bacteria
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Exogenous and Endogenous Induction of the Histidine-degrading Enzymes in Aerobacter aerogenes
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Initiation of Bacillus subtilis sporulation by the stringent response to partial amino acid deprivation.
inferredcites →https://doi.org/10.1016/s0092-8674(01)00572-4openalex-snapshot
Bacillus subtilis Glutamine Synthetase Controls Gene Expression through a Protein-Protein Interaction with Transcription Factor TnrA
inferredcites →https://doi.org/10.1016/s1096-7176(03)00009-0openalex-snapshot
Transcriptional profiling of gene expression in response to glucose in Bacillus subtilis: regulation of the central metabolic pathways
inferredcites →https://doi.org/10.1021/pr034020mopenalex-snapshot
Quantitative Metabolome Analysis Using Capillary Electrophoresis Mass Spectrometry
inferredcites →https://doi.org/10.1038/sj.emboj.7600423openalex-snapshot
An alternative strategy for bacterial ribosome synthesis: Bacillus subtilis rRNA transcription regulation
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Expression of the Bacillus subtilis gabP gene is regulated independently in response to nitrogen and amino acid availability
inferredcites →https://doi.org/10.1046/j.1365-2958.1997.3881754.xopenalex-snapshot
Role of the transcriptional activator RocR in the arginine‐degradation pathway of Bacillus subtilis
inferredcites →https://doi.org/10.1046/j.1365-2958.1997.5511919.xopenalex-snapshot
Cloning and characterization of a relA/spoT homologue from Bacillus subtilis
inferredcites →https://doi.org/10.1046/j.1365-2958.1998.00663.xopenalex-snapshot
Regulated transcription of Clostridium difficile toxin genes
inferredcites →https://doi.org/10.1046/j.1365-2958.1998.01111.xopenalex-snapshot
Transcriptional activation of the glycolytic las operon and catabolite repression of the gal operon in Lactococcus lactis are mediated by the catabolite control protein CcpA
inferredcites →https://doi.org/10.1046/j.1365-2958.1999.01333.xopenalex-snapshot
Regulation of nitrogen metabolism in Bacillus subtilis: vive la différence!
inferredcites →https://doi.org/10.1046/j.1365-2958.1999.01519.xopenalex-snapshot
Co‐ordination of Legionella pneumophila virulence with entry into stationary phase by ppGpp
inferredcites →https://doi.org/10.1046/j.1365-2958.2001.02328.xopenalex-snapshot
Catabolite repression mediated by the CcpA protein in Bacillus subtilis: novel modes of regulation revealed by whole-genome analyses
inferredcites →https://doi.org/10.1046/j.1365-2958.2001.02470.xopenalex-snapshot
Pleiotropic transcriptional repressor CodY senses the intracellular pool of branched‐chain amino acids in Lactococcus lactis
inferredcites →https://doi.org/10.1046/j.1365-2958.2002.02751.xopenalex-snapshot
Regulation of the Bacillus subtilis ccpC gene by CcpA and CcpC
inferredcites →https://doi.org/10.1046/j.1365-2958.2002.03003.xopenalex-snapshot
Direct and indirect roles of CcpA in regulation of Bacillus subtilis Krebs cycle genes
inferredcites →https://doi.org/10.1046/j.1365-2958.2002.03034.xopenalex-snapshot
Control of the glycolytic gapA operon by the catabolite control protein A in Bacillus subtilis: a novel mechanism of CcpA‐mediated regulation
inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03567.xopenalex-snapshot
Identification of additional TnrA‐regulated genes of Bacillus subtilis associated with a TnrA box
inferredcites →https://doi.org/10.1073/pnas.101126598openalex-snapshot
Regulation of toxin synthesis in Clostridium difficile by an alternative RNA polymerase sigma factor
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.93.17.8841openalex-snapshot
TnrA, a transcription factor required for global nitrogen regulation in Bacillus subtilis.
inferredcites →https://doi.org/10.1073/pnas.96.18.10290openalex-snapshot
An enhancer element located downstream of the major glutamate dehydrogenase gene of Bacillus subtilis
inferredcites →https://doi.org/10.1074/jbc.275.3.1773openalex-snapshot
The HPr Kinase from Bacillus subtilis Is a Homo-oligomeric Enzyme Which Exhibits Strong Positive Cooperativity for Nucleotide and Fructose 1,6-Bisphosphate Binding
inferredcites →https://doi.org/10.1074/jbc.m208722200openalex-snapshot
Guanine Nucleotides Guanosine 5′-Diphosphate 3′-Diphosphate and GTP Co-operatively Regulate the Production of an Antibiotic Bacilysin in Bacillus subtilis
inferredcites →https://doi.org/10.1074/jbc.m502349200openalex-snapshot
The Lactococcus lactis CodY Regulon
inferredcites →https://doi.org/10.1074/jbc.m601661200openalex-snapshot
Regulation of Glutamine and Glutamate Metabolism by GlnR and GlnA in Streptococcus pneumoniae
inferredcites →https://doi.org/10.1078/1438-4221-00111openalex-snapshot
Regulation of virulence genes in Listeria
inferredcites →https://doi.org/10.1093/emboj/20.15.3928openalex-snapshot
Mutations lowering the phosphatase activity of HPr kinase/phosphatase switch off carbon metabolism
inferredcites →https://doi.org/10.1093/oxfordjournals.jbchem.a022454openalex-snapshot
Regulation of the Bacillus subtilis Phosphotransacetylase Gene
inferredcites →https://doi.org/10.1093/oxfordjournals.jbchem.a123365openalex-snapshot
Purification and Characterization of a Repressor for the Bacillus cereus glnRA Operon
inferredcites →https://doi.org/10.1099/00221287-148-6-1805openalex-snapshot
HPr kinase/phosphatase of Bacillus subtilis: expression of the gene and effects of mutations on enzyme activity, growth and carbon catabolite repression
inferredcites →https://doi.org/10.1099/jmm.0.46984-0openalex-snapshot
CodY-affected transcriptional gene expression of Streptococcus pyogenes during growth in human blood
inferredcites →https://doi.org/10.1099/mic.0.26013-0openalex-snapshot
Specificity of the interaction of RocR with the rocG–rocA intergenic region in Bacillus subtilis
inferredcites →https://doi.org/10.1099/mic.0.26479-0openalex-snapshot
The regulatory link between carbon and nitrogen metabolism in Bacillus subtilis: regulation of the gltAB operon by the catabolite control protein CcpA
inferredcites →https://doi.org/10.1099/mic.0.28186-0openalex-snapshot
Overall control of nitrogen metabolism in Lactococcus lactis by CodY, and possible models for CodY regulation in Firmicutes
inferredcites →https://doi.org/10.1101/gad.874201openalex-snapshot
Bacillus subtilis CodY represses early-stationary-phase genes by sensing GTP levels
inferredcites →https://doi.org/10.1111/j.1365-2958.1995.tb02280.xopenalex-snapshot
Protein kinase‐dependent HPr/CcpA interaction links glycolytic activity to carbon catabolite repression in Gram‐positive bacteria
inferredcites →https://doi.org/10.1111/j.1365-2958.1995.tb02378.xopenalex-snapshot
A gene required for nutritional repression of the Bacillus subtilis dipeptide permease operon
inferredcites →https://doi.org/10.1111/j.1365-2958.2004.04135.xopenalex-snapshot
Activation of the Bacillus subtilis global regulator CodY by direct interaction with branched‐chain amino acids
inferredcites →https://doi.org/10.1111/j.1365-2958.2004.04136.xopenalex-snapshot
Intracellular effectors regulating the activity of the Lactococcus lactis CodY pleiotropic transcription regulator
inferredcites →https://doi.org/10.1111/j.1365-2958.2005.04634.xopenalex-snapshot
Bacillus subtilis ilvB operon: an intersection of global regulons
inferredcites →https://doi.org/10.1111/j.1365-2958.2005.04635.xopenalex-snapshot
Elaborate transcription regulation of the Bacillus subtilis ilv‐leu operon involved in the biosynthesis of branched‐chain amino acids through global regulators of CcpA, CodY and TnrA
inferredcites →https://doi.org/10.1111/j.1365-2958.2006.05410.xopenalex-snapshot
Positive regulation of Bacillus subtilis ackA by CodY and CcpA: establishing a potential hierarchy in carbon flow
inferredcites →https://doi.org/10.1111/j.1365-2958.2007.05597.xopenalex-snapshot
Characterization of relA and codY mutants of Listeria monocytogenes: identification of the CodY regulon and its role in virulence
inferredcites →https://doi.org/10.1111/j.1365-2958.2007.05816.xopenalex-snapshot
A regulatory protein–protein interaction governs glutamate biosynthesis in Bacillus subtilis: the glutamate dehydrogenase RocG moonlights in controlling the transcription factor GltC
inferredcites →https://doi.org/10.1111/j.1365-2958.2007.05906.xopenalex-snapshot
Repression of Clostridium difficile toxin gene expression by CodY
inferredcites →https://doi.org/10.1111/j.1432-1033.1997.t01-1-00735.xopenalex-snapshot
Transcription Analysis of the Genes tcdA‐E of the Pathogenicity Locus of Clostridium Difficile
inferredcites →https://doi.org/10.1111/j.1742-4658.2005.04682.xopenalex-snapshot
Quantitative interdependence of coeffectors, CcpA and cre in carbon catabolite regulation of Bacillus subtilis
inferredcites →https://doi.org/10.1128/.180.23.6298-6305.1998openalex-snapshot
Role and Regulation of Bacillus subtilis Glutamate Dehydrogenase Genes
inferredcites →https://doi.org/10.1128/.180.23.6316-6324.1998openalex-snapshot
A Homolog of CcpA Mediates Catabolite Control in Listeria monocytogenes but Not Carbon Source Regulation of Virulence Genes
inferredcites →https://doi.org/10.1128/9781555817992openalex-snapshot
Bacillus subtilis and Its Closest Relatives
inferredcites →https://doi.org/10.1128/9781555817992.ch11openalex-snapshot
Carbohydrate Uptake and Metabolism
inferredcites →https://doi.org/10.1128/9781555817992.ch5openalex-snapshot
Biosynthesis and Function of Membrane Lipids
inferredcites →https://doi.org/10.1128/aac.50.4.1183-1194.2006openalex-snapshot
Staphylococcus aureus CcpA Affects Virulence Determinant Production and Antibiotic Resistance
inferredcites →https://doi.org/10.1128/aem.69.6.3061-3068.2003openalex-snapshot
CodY-Regulated Aminotransferases AraT and BcaT Play a Major Role in the Growth of Lactococcus lactis in Milk by Regulating the Intracellular Pool of Amino Acids
inferredcites →https://doi.org/10.1128/aem.70.9.5244-5251.2004openalex-snapshot
Molecular Characterization of CcpA and Involvement of This Protein in Transcriptional Regulation of Lactate Dehydrogenase and Pyruvate Formate-Lyase in the Ruminal Bacterium Streptococcus bovis
inferredcites →https://doi.org/10.1128/iai.01143-06openalex-snapshot
Isolation and Characterization of Biofilm Formation-Defective Mutants of Staphylococcus aureus
inferredcites →https://doi.org/10.1128/iai.70.10.5454-5461.2002openalex-snapshot
Role of RegM, a Homologue of the Catabolite Repressor Protein CcpA, in the Virulence of Streptococcus pneumoniae
inferredcites →https://doi.org/10.1128/jb.00544-06openalex-snapshot
Feedback-Resistant Mutations in Bacillus subtilis Glutamine Synthetase Are Clustered in the Active Site
inferredcites →https://doi.org/10.1128/jb.00972-06openalex-snapshot
Interference of Components of the Phosphoenolpyruvate Phosphotransferase System with the Central Virulence Gene Regulator PrfA ofListeria monocytogenes
inferredcites →https://doi.org/10.1128/jb.146.2.605-613.1981openalex-snapshot
Response of Guanosine 5′-Triphosphate Concentration to Nutritional Changes and Its Significance for Bacillus subtilis Sporulation
inferredcites →https://doi.org/10.1128/jb.158.1.379-382.1984openalex-snapshot
2-Ketoglutarate and the regulation of aconitase and histidase formation in Bacillus subtilis
inferredcites →https://doi.org/10.1128/jb.169.7.3062-3067.1987openalex-snapshot
Purification of aconitase from Bacillus subtilis and correlation of its N-terminal amino acid sequence with the sequence of the citB gene
inferredcites →https://doi.org/10.1128/jb.171.9.4718-4727.1989openalex-snapshot
Positive regulation of glutamate biosynthesis in Bacillus subtilis
inferredcites →https://doi.org/10.1128/jb.175.22.7348-7355.1993openalex-snapshot
Regulation of the Bacillus subtilis acetate kinase gene by CcpA
inferredcites →https://doi.org/10.1128/jb.176.15.4527-4533.1994openalex-snapshot
Catabolite regulation of Bacillus subtilis acetate and acetoin utilization genes by CcpA
inferredcites →https://doi.org/10.1128/jb.176.15.4669-4679.1994openalex-snapshot
Identification of two distinct Bacillus subtilis citrate synthase genes
inferredcites →https://doi.org/10.1128/jb.176.15.4680-4690.1994openalex-snapshot
Transcriptional regulation of Bacillus subtilis citrate synthase genes
inferredcites →https://doi.org/10.1128/jb.176.7.1894-1902.1994openalex-snapshot
Catabolite repression of the Bacillus subtilis hut operon requires a cis-acting site located downstream of the transcription initiation site
inferredcites →https://doi.org/10.1128/jb.177.19.5686-5695.1995openalex-snapshot
Sites required for GltC-dependent regulation of Bacillus subtilis glutamate synthase expression
inferredcites →https://doi.org/10.1128/jb.178.13.3779-3784.1996openalex-snapshot
Role of CodY in regulation of the Bacillus subtilis hut operon
inferredcites →https://doi.org/10.1128/jb.178.2.560-563.1996openalex-snapshot
A Bacillus subtilis malate dehydrogenase gene
inferredcites →https://doi.org/10.1128/jb.178.20.5910-5915.1996openalex-snapshot
CodY is required for nutritional repression of Bacillus subtilis genetic competence
inferredcites →https://doi.org/10.1128/jb.178.8.2450-2454.1996openalex-snapshot
Autogenous regulation of the Bacillus subtilis glnRA operon
inferredcites →https://doi.org/10.1128/jb.179.17.5494-5501.1997openalex-snapshot
Expression of the Bacillus subtilis ureABC operon is controlled by multiple regulatory factors including CodY, GlnR, TnrA, and Spo0H
inferredcites →https://doi.org/10.1128/jb.180.24.6649-6654.1998openalex-snapshot
Expression of the Bacillus subtilis acsA Gene: Position and Sequence Context Affect cre -Mediated Carbon Catabolite Repression
inferredcites →https://doi.org/10.1128/jb.181.22.6889-6897.1999openalex-snapshot
Catabolite Regulation of the pta Gene as Part of Carbon Flow Pathways in Bacillus subtilis
inferredcites →https://doi.org/10.1128/jb.181.7.2059-2066.1999openalex-snapshot
Role of BkdR, a Transcriptional Activator of the SigL-Dependent Isoleucine and Valine Degradation Pathway in Bacillus subtilis
inferredcites →https://doi.org/10.1128/jb.181.9.2883-2888.1999openalex-snapshot
trans -Acting Factors Affecting Carbon Catabolite Repression of the hut Operon in Bacillus subtilis
inferredcites →https://doi.org/10.1128/jb.183.8.2497-2504.2001openalex-snapshot
Regulation of the Acetoin Catabolic Pathway Is Controlled by Sigma L in Bacillus subtilis
inferredcites →https://doi.org/10.1128/jb.184.14.3923-3930.2002openalex-snapshot
RelA Protein Is Involved in Induction of Genetic Competence in Certain Bacillus subtilis Strains by Moderating the Level of Intracellular GTP
inferredcites →https://doi.org/10.1128/jb.184.17.4690-4698.2002openalex-snapshot
Genomic Variability of O Islands Encoding Tellurite Resistance in Enterohemorrhagic Escherichia coli O157:H7 Isolates
inferredcites →https://doi.org/10.1128/jb.184.18.5174-5178.2002openalex-snapshot
Insufficient Expression of theilv-leuOperon Encoding Enzymes of Branched-Chain Amino Acid Biosynthesis Limits Growth of aBacillus subtilis ccpAMutant
inferredcites →https://doi.org/10.1128/jb.184.21.5971-5978.2002openalex-snapshot
Environmental Response and Autoregulation of Clostridium difficile TxeR, a Sigma Factor for Toxin Gene Expression
inferredcites →https://doi.org/10.1128/jb.184.21.6060-6064.2002openalex-snapshot
Roles of PucR, GlnR, and TnrA in Regulating Expression of the Bacillus subtilis ure P3 Promoter
inferredcites →https://doi.org/10.1128/jb.184.3.621-628.2002openalex-snapshot
Listeria monocytogenes relAandhptMutants Are Impaired in Surface-Attached Growth and Virulence
inferredcites →https://doi.org/10.1128/jb.184.9.2500-2520.2002openalex-snapshot
Bacillus subtilisfunctional genomics: global characterization of the stringent response by proteome and transcriptome analysis
inferredcites →https://doi.org/10.1128/jb.185.10.3118-3126.2003openalex-snapshot
CodY Is a Nutritional Repressor of Flagellar Gene Expression inBacillus subtilis
inferredcites →https://doi.org/10.1128/jb.185.14.4003-4010.2003openalex-snapshot
HPr Kinase/Phosphorylase, the Sensor Enzyme of Catabolite Repression in Gram-Positive Bacteria: Structural Aspects of the Enzyme and the Complex with Its Protein Substrate
inferredcites →https://doi.org/10.1128/jb.185.5.1672-1680.2003openalex-snapshot
Complex Regulation of theBacillus subtilisAconitase Gene
inferredcites →https://doi.org/10.1128/jb.185.6.1911-1922.2003openalex-snapshot
Additional Targets of the Bacillus subtilis Global Regulator CodY Identified by Chromatin Immunoprecipitation and Genome-Wide Transcript Analysis
inferredcites →https://doi.org/10.1128/jb.186.11.3392-3398.2004openalex-snapshot
CcpA-Dependent Regulation of Bacillus subtilis Glutamate Dehydrogenase Gene Expression
inferredcites →https://doi.org/10.1128/jb.186.11.3399-3407.2004openalex-snapshot
Modulation of Activity of Bacillus subtilis Regulatory Proteins GltC and TnrA by Glutamate Dehydrogenase
inferredcites →https://doi.org/10.1128/jb.186.16.5221-5229.2004openalex-snapshot
The CcpA Protein Is Necessary for Efficient Sporulation and Enterotoxin Gene (cpe) Regulation inClostridium perfringens
inferredcites →https://doi.org/10.1128/jb.186.23.7971-7979.2004openalex-snapshot
Negative Transcriptional Regulation of the ilv-leu Operon for Biosynthesis of Branched-Chain Amino Acids through the Bacillus subtilis Global Regulator TnrA
inferredcites →https://doi.org/10.1128/jb.187.2.512-521.2005openalex-snapshot
Probing Direct Interactions between CodY and theoppDPromoter ofLactococcus lactis
inferredcites →https://doi.org/10.1128/jb.187.22.7826-7839.2005openalex-snapshot
Catabolite Repression and Activation in Bacillus subtilis : Dependency on CcpA, HPr, and HprK
inferredcites →https://doi.org/10.1128/jb.187.24.8340-8349.2005openalex-snapshot
Catabolite Control Protein A (CcpA) Contributes to Virulence and Regulation of Sugar Metabolism in Streptococcus pneumoniae
inferredcites →https://doi.org/10.1128/jb.188.1.179-190.2006openalex-snapshot
CcpC-Dependent Regulation of citB and lmo0847 in Listeria monocytogenes
inferredcites →https://doi.org/10.1128/jb.188.7.2578-2585.2006openalex-snapshot
Cross-Regulation of the Bacillus subtilis glnRA and tnrA Genes Provides Evidence for DNA Binding Site Discrimination by GlnR and TnrA
inferredcites →https://doi.org/10.1128/jb.188.9.3280-3289.2006openalex-snapshot
Identification and Functional Characterization of theLactococcus lactisCodY-Regulated Branched-Chain Amino Acid Permease BcaP (CtrA)
inferredcites →https://doi.org/10.1128/mmbr.00024-06openalex-snapshot
How Phosphotransferase System-Related Protein Phosphorylation Regulates Carbohydrate Metabolism in Bacteria
inferredcites →https://doi.org/10.1128/mmbr.58.3.466-490.1994openalex-snapshot
The leucine-responsive regulatory protein, a global regulator of metabolism in Escherichia coli
inferredcites →https://doi.org/10.1128/mmbr.67.4.475-490.2003openalex-snapshot
CcpA-Dependent Carbon Catabolite Repression in Bacteria
inferredcites →https://doi.org/10.1159/000089650openalex-snapshot
How Seryl-Phosphorylated HPr Inhibits PrfA, a Transcription Activator of Listeria monocytogenes Virulence Genes
inferredcites →https://doi.org/10.1159/000096463openalex-snapshot
Transcriptome Analysis of Temporal Regulation of Carbon Metabolism by CcpA in Bacillus subtilis Reveals Additional Target Genes
inferredcites →https://doi.org/10.1186/1471-2180-7-2openalex-snapshot
Integration of regulatory signals through involvement of multiple global regulators: control of the Escherichia coli gltBDF operon by Lrp, IHF, Crp, and ArgR

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Regulation of cid and lrg expression by CodY in Streptococcus mutans
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Condition‐dependent resource allocation strategy governed by CodY regulator in Bacillus subtilis
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Genome‐wide transcriptomic responses of a human isolate of L actobacillus plantarum exposed to p‐coumaric acid stress
inferred← citeshttps://doi.org/10.1007/978-3-642-30141-4_67openalex-snapshot
Lignocellulose-Decomposing Bacteria and Their Enzyme Systems
inferred← citeshttps://doi.org/10.1007/s00203-023-03652-3openalex-snapshot
A review on surfactin: molecular regulation of biosynthesis
inferred← citeshttps://doi.org/10.1007/s00253-017-8459-2openalex-snapshot
Improvement of glycerol catabolism in Bacillus licheniformis for production of poly-γ-glutamic acid
inferred← citeshttps://doi.org/10.1007/s00253-021-11594-3openalex-snapshot
Protein expression profiling of Staphylococcus aureus in response to the bacteriocin bovicin HC5
inferred← citeshttps://doi.org/10.1007/s00284-016-0998-8openalex-snapshot
Transcriptional Profiling Analysis of Bacillus subtilis in Response to High Levels of Fe3+
inferred← citeshttps://doi.org/10.1007/s00284-016-1120-yopenalex-snapshot
Late-Exponential Gene Expression in codY-Deficient Bacillus anthracis in a Host-Like Environment
inferred← citeshttps://doi.org/10.1007/s00284-020-02161-6openalex-snapshot
Complete Genome Sequence of Lactobacillus hilgardii LMG 7934, Carrying the Gene Encoding for the Novel PII-Like Protein PotN
inferred← citeshttps://doi.org/10.1007/s00285-017-1118-5openalex-snapshot
Optimal resource allocation enables mathematical exploration of microbial metabolic configurations
inferred← citeshttps://doi.org/10.1007/s00449-013-0959-6openalex-snapshot
Enhancement of adenosine production by Bacillus subtilis CGMCC 4484 through metabolic flux analysis and simplified feeding strategies
inferred← citeshttps://doi.org/10.1007/s10295-018-2024-6openalex-snapshot
Production of pikromycin using branched chain amino acid catabolism in Streptomyces venezuelae ATCC 15439
inferred← citeshttps://doi.org/10.1007/s10482-017-0911-xopenalex-snapshot
Nitrogen assimilation in denitrifier Bacillus azotoformans LMG 9581T
inferred← citeshttps://doi.org/10.1007/s10529-012-1038-9openalex-snapshot
Metabolic shifts: a fitness perspective for microbial cell factories
inferred← citeshttps://doi.org/10.1007/s11274-021-03028-zopenalex-snapshot
Lactic acid production using cheese whey based medium in a stirred tank reactor by a ccpA mutant of Lacticaseibacillus casei
inferred← citeshttps://doi.org/10.1007/s11274-022-03460-9openalex-snapshot
Engineering of global transcription factors in Bacillus, a genetic tool for increasing product yields: a bioprocess overview
inferred← citeshttps://doi.org/10.1007/s11306-018-1339-7openalex-snapshot
Metabolite secretion in microorganisms: the theory of metabolic overflow put to the test
inferred← citeshttps://doi.org/10.1007/s11427-010-4106-1openalex-snapshot
Comparative proteome analysis of alkaliphilic Bacillus sp. N16-5 grown on different carbon sources
inferred← citeshttps://doi.org/10.1007/s11694-025-03259-wopenalex-snapshot
Comparative investigation of Mycotoxin detoxification mechanisms by lactic acid bacteria (Lactobacillus species) and non-lactic acid bacteria
inferred← citeshttps://doi.org/10.1007/s12010-021-03619-4openalex-snapshot
Metabolic Engineering of Central Carbon Metabolism of Bacillus licheniformis for Enhanced Production of Poly-γ-glutamic Acid
inferred← citeshttps://doi.org/10.1007/s12161-014-9999-zopenalex-snapshot
Evaluating Potential Markers of Spoilage Foods Using a Metabolic Profiling Approach
inferred← citeshttps://doi.org/10.1007/s12257-020-0104-8openalex-snapshot
Engineering Bacillus subtilis Cells as Factories: Enzyme Secretion and Value-added Chemical Production
inferred← citeshttps://doi.org/10.1007/s12602-020-09707-xopenalex-snapshot
Impact of Supplements on Enhanced Activity of Bacillus amyloliquefaciens BmB1 Against Pythium aphanidermatum Through Lipopeptide Modulation
inferred← citeshttps://doi.org/10.1007/s43393-023-00229-5openalex-snapshot
Transcriptional modulation of the global regulator CodY using a conditional CRISPRi system in Bacillus licheniformis
inferred← citeshttps://doi.org/10.1007/springerreference_3662openalex-snapshot
Cellulose-decomposing Bacteria and Their Enzyme Systems
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.02454-5openalex-snapshot
Regulation of Carbon Assimilation in Bacteria
inferred← citeshttps://doi.org/10.1016/b978-0-12-812705-6.00006-xopenalex-snapshot
Lipopeptide Biosurfactants From Bacillus Species
inferred← citeshttps://doi.org/10.1016/b978-0-12-821477-0.00002-7openalex-snapshot
Bacillus subtilis-based microbial cell factories
inferred← citeshttps://doi.org/10.1016/b978-012373944-5.00067-5openalex-snapshot
Regulation of Carbon Assimilation in Bacteria
inferred← citeshttps://doi.org/10.1016/bs.abr.2018.11.004openalex-snapshot
Nitrogen storage and cycling in trees
inferred← citeshttps://doi.org/10.1016/j.aca.2023.340977openalex-snapshot
Facile synthesis of amino-functionalized magnetic materials for efficient enrichment of anionic metabolites from biological samples
inferred← citeshttps://doi.org/10.1016/j.arr.2014.05.004openalex-snapshot
Krebs cycle intermediates regulate DNA and histone methylation: Epigenetic impact on the aging process
inferred← citeshttps://doi.org/10.1016/j.bej.2013.01.008openalex-snapshot
Metabolic studies of γ-polyglutamic acid production in Bacillus licheniformis by small-scale continuous cultivations
inferred← citeshttps://doi.org/10.1016/j.bej.2022.108528openalex-snapshot
Metabolic engineering of Bacillus subtilis 168 for the utilization of arabinose to synthesize the antifungal lipopeptide fengycin
inferred← citeshttps://doi.org/10.1016/j.bej.2024.109375openalex-snapshot
Biokinetics modelling of lycopene-producing E. coli fermentation using PAT methodology
inferred← citeshttps://doi.org/10.1016/j.biortech.2025.132702openalex-snapshot
Enhancing alkaline protease production in Bacillus amyloliquefaciens via surfactin-mediated mechanisms and metabolic engineering
inferred← citeshttps://doi.org/10.1016/j.biortech.2026.134441openalex-snapshot
Directed evolution of a serine protease LsPLAase in Bacillus subtilis for high-yield secretory production and efficient depolymerization of polylactic acid
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2016.11.003openalex-snapshot
Metabolic engineering of Bacillus subtilis fueled by systems biology: Recent advances and future directions
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2018.12.007openalex-snapshot
Regulation of glycolytic flux and overflow metabolism depending on the source of energy generation for energy demand
inferred← citeshttps://doi.org/10.1016/j.bpj.2019.09.035openalex-snapshot
Model of a Kinetically Driven Crosstalk between Paralogous Protein Encounter Complexes
inferred← citeshttps://doi.org/10.1016/j.carbpol.2020.117115openalex-snapshot
Biosynthesis of low-molecular-weight mannan using metabolically engineered Bacillus subtilis 168
inferred← citeshttps://doi.org/10.1016/j.carbpol.2025.123829openalex-snapshot
Promoting proliferation of Lactobacillus plantarum FN107 by Dendrobium oligosaccharide-mediated elimination of carbon catabolite repression
inferred← citeshttps://doi.org/10.1016/j.cell.2021.12.001openalex-snapshot
A segmentation clock patterns cellular differentiation in a bacterial biofilm
inferred← citeshttps://doi.org/10.1016/j.chom.2015.05.006openalex-snapshot
The PAMP c-di-AMP Is Essential for Listeria monocytogenes Growth in Rich but Not Minimal Media due to a Toxic Increase in (p)ppGpp
inferred← citeshttps://doi.org/10.1016/j.chroma.2021.462531openalex-snapshot
Optimization and validation of capillary electrophoresis- and gas chromatography-tandem mass spectrometry methods for the analysis of intermediate metabolites in glycolysis and pentose phosphate pathways within biological samples
inferred← citeshttps://doi.org/10.1016/j.coisb.2018.10.001openalex-snapshot
Interrogating metabolism as an electron flow system
inferred← citeshttps://doi.org/10.1016/j.envint.2025.109844openalex-snapshot
Recombinant glutamine synthetase originating from high ammonium-assimilating Bacillus subtilis effectively reduces NH3 emissions and enhances the conversion into amino acids in liquid manure
inferred← citeshttps://doi.org/10.1016/j.fbio.2023.103056openalex-snapshot
Biotransformation of okara (soybean residue) through solid-state fermentation using probiotic Bacillus subtilis and Bacillus coagulans
inferred← citeshttps://doi.org/10.1016/j.fm.2018.01.007openalex-snapshot
Staphylococcus aureus undergoes major transcriptional reorganization during growth with Enterococcus faecalis in milk
inferred← citeshttps://doi.org/10.1016/j.fm.2021.103905openalex-snapshot
Integrative multiomics analysis of the acid stress response of Oenococcus oeni mutants at different growth stages
inferred← citeshttps://doi.org/10.1016/j.fm.2024.104599openalex-snapshot
Soy protein hydrolysates induce menaquinone-7 biosynthesis by enhancing the biofilm formation of Bacillus subtilis natto
inferred← citeshttps://doi.org/10.1016/j.fm.2026.105066openalex-snapshot
Matrix matters: Context-driven metabolic shifts in Bacillus cereus and Bacillus subtilis
inferred← citeshttps://doi.org/10.1016/j.foodres.2022.111332openalex-snapshot
Characterization of the nitrite production of mesophilic spore-forming bacteria during the handling of reconstituted infant formula
inferred← citeshttps://doi.org/10.1016/j.foodres.2025.115851openalex-snapshot
Unraveling the microbial community and succession during the maturation of Chinese cereal vinegar Daqu and their relationships with flavor formation
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2023.126407openalex-snapshot
Sequence composition and location of CRE motifs affect the binding ability of CcpA protein
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2017.10.029openalex-snapshot
The genetic basis underlying variation in production of the flavour compound diacetyl by Lactobacillus rhamnosus strains in milk
inferred← citeshttps://doi.org/10.1016/j.ijfoodmicro.2019.108419openalex-snapshot
Sucrose enhances colour formation in dry sausages by up-regulating gene expression of nitric oxide synthase in Staphylococcus vitulinus
inferred← citeshttps://doi.org/10.1016/j.isci.2019.10.009openalex-snapshot
Glucose-Induced Cyclic Lipopeptides Resistance in Bacteria via ATP Maintenance through Enhanced Glycolysis
inferred← citeshttps://doi.org/10.1016/j.isci.2021.102400openalex-snapshot
A new CcpA binding site plays a bidirectional role in carbon catabolism in Bacillus licheniformis
inferred← citeshttps://doi.org/10.1016/j.isci.2022.105242openalex-snapshot
Glutamate catabolism during sporulation determines the success of the future spore germination
inferred← citeshttps://doi.org/10.1016/j.isci.2024.111386openalex-snapshot
Intrinsically robust and scalable biofilm segmentation under diverse physical growth conditions
inferred← citeshttps://doi.org/10.1016/j.jare.2022.09.003openalex-snapshot
Understanding and application of Bacillus nitrogen regulation: A synthetic biology perspective
inferred← citeshttps://doi.org/10.1016/j.jbiosc.2015.08.012openalex-snapshot
Metabolome analysis reveals the effect of carbon catabolite control on the poly(γ-glutamic acid) biosynthesis of Bacillus licheniformis ATCC 9945
inferred← citeshttps://doi.org/10.1016/j.jbiosc.2020.04.011openalex-snapshot
Poly-γ-glutamic acid production by Bacillus subtilis 168 using glucose as the sole carbon source: A metabolomic analysis
inferred← citeshttps://doi.org/10.1016/j.jbiotec.2014.03.025openalex-snapshot
13C-metabolic flux analysis in heterologous cellulase production by Bacillus subtilis genome-reduced strain
inferred← citeshttps://doi.org/10.1016/j.jbiotec.2016.05.026openalex-snapshot
Impacts of proline on the central metabolism of an industrial erythromycin-producing strain Saccharopolyspora erythraea via 13 C labeling experiments
inferred← citeshttps://doi.org/10.1016/j.jbiotec.2019.04.027openalex-snapshot
Glucose limitation and glucose uptake rate determines metabolite production and sporulation in high cell density continuous cultures of Bacillus amyloliquefaciens 83
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2025.138867openalex-snapshot
Multi-omics analysis of Stenotrophomonas maltophilia S-11 reveals its potential for Pb2+ bioremediation in contaminated soil
inferred← citeshttps://doi.org/10.1016/j.jmb.2011.06.012openalex-snapshot
Roadblock Repression of Transcription by Bacillus subtilis CodY
inferred← citeshttps://doi.org/10.1016/j.jmb.2011.08.003openalex-snapshot
Indirect Repression by Bacillus subtilis CodY via Displacement of the Activator of the Proline Utilization Operon
inferred← citeshttps://doi.org/10.1016/j.jmb.2025.169123openalex-snapshot
The SinR·SlrR Heteromer Attenuates Transcription of a Long Operon of Flagellar Genes in Bacillus subtilis
inferred← citeshttps://doi.org/10.1016/j.jprot.2012.06.002openalex-snapshot
Proteomic analysis of Bacillus thuringiensis ΔphaC mutant BMB171/PHB−1 reveals that the PHB synthetic pathway warrants normal carbon metabolism
inferred← citeshttps://doi.org/10.1016/j.jprot.2023.105007openalex-snapshot
S-layer is a key element in metabolic response and entry into the stationary phase in Bacillus cereus AH187
inferred← citeshttps://doi.org/10.1016/j.lwt.2024.116880openalex-snapshot
Co-fermentation of hot-pressed rapeseed meal with multiple strains and cellulase: Evaluating changes in protein quality and metabolite profiles
inferred← citeshttps://doi.org/10.1016/j.lwt.2025.118630openalex-snapshot
Aroma-producing profiles, degradation mechanism of a β-carotene-degrading Bacillus thuringiensis strain
inferred← citeshttps://doi.org/10.1016/j.mec.2023.e00223openalex-snapshot
Adaptive laboratory evolution of Bacillus subtilis to overcome toxicity of lignocellulosic hydrolysate derived from Distiller's dried grains with solubles (DDGS)
inferred← citeshttps://doi.org/10.1016/j.mib.2009.01.009openalex-snapshot
Allostery in the LacI/GalR family: variations on a theme
inferred← citeshttps://doi.org/10.1016/j.mib.2026.102757openalex-snapshot
Carbon catabolite repression in Gram-positive bacteria, including the recently developed insights
inferred← citeshttps://doi.org/10.1016/j.mib.2026.102765openalex-snapshot
Discovery of new mechanisms to control metabolism and homeostasis in Bacillus subtilis
inferred← citeshttps://doi.org/10.1016/j.micres.2014.12.002openalex-snapshot
Polyphosphate kinase of Lysinibacillus sphaericus and its effects on accumulation of polyphosphate and bacterial growth
inferred← citeshttps://doi.org/10.1016/j.micres.2017.12.014openalex-snapshot
Volatiles produced by Bacillus mojavensis RRC101 act as plant growth modulators and are strongly culture-dependent
inferred← citeshttps://doi.org/10.1016/j.plantsci.2018.02.021openalex-snapshot
Seasonal nitrogen cycling in temperate trees: Transport and regulatory mechanisms are key missing links
inferred← citeshttps://doi.org/10.1016/j.preteyeres.2012.03.004openalex-snapshot
Bacterial endophthalmitis in the age of outpatient intravitreal therapies and cataract surgeries: Host–microbe interactions in intraocular infection
inferred← citeshttps://doi.org/10.1016/j.procbio.2017.02.016openalex-snapshot
Improved cultivation of gdhA derivative Pasteurella multocida B:2 for high density of viable cells through in situ ammonium removal using cation-exchange resin for use as animal vaccine
inferred← citeshttps://doi.org/10.1016/j.resmic.2014.09.010openalex-snapshot
Regulation of toxin gene expression in Clostridium perfringens
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2022.153169openalex-snapshot
Transcriptomics and proteomics revealed the psychrotolerant and antibiotic-resistant mechanisms of strain Pseudomonas psychrophila RNC-1 capable of assimilatory nitrate reduction and aerobic denitrification
inferred← citeshttps://doi.org/10.1016/j.synbio.2023.03.009openalex-snapshot
Microbial synthesis of bacitracin: Recent progress, challenges, and prospects
inferred← citeshttps://doi.org/10.1016/j.tim.2008.04.002openalex-snapshot
The role of complex carbohydrate catabolism in the pathogenesis of invasive streptococci
inferred← citeshttps://doi.org/10.1016/j.watres.2025.124099openalex-snapshot
Responses of viral communities in aerobic biofilms under antibiotic stress
inferred← citeshttps://doi.org/10.1016/j.ymben.2010.10.001openalex-snapshot
Physical interactions between tricarboxylic acid cycle enzymes in Bacillus subtilis: Evidence for a metabolon
inferred← citeshttps://doi.org/10.1016/j.ymben.2014.02.007openalex-snapshot
Consolidated conversion of protein waste into biofuels and ammonia using Bacillus subtilis
inferred← citeshttps://doi.org/10.1016/j.ymben.2016.01.008openalex-snapshot
Production of specific-molecular-weight hyaluronan by metabolically engineered Bacillus subtilis 168
inferred← citeshttps://doi.org/10.1016/j.ymben.2017.12.004openalex-snapshot
Changes of DNA topology affect the global transcription landscape and allow rapid growth of a Bacillus subtilis mutant lacking carbon catabolite repression
inferred← citeshttps://doi.org/10.1016/j.ymben.2018.05.006openalex-snapshot
Advances and prospects of Bacillus subtilis cellular factories: From rational design to industrial applications
inferred← citeshttps://doi.org/10.1016/j.ymben.2018.08.001openalex-snapshot
Boosting heterologous protein production yield by adjusting global nitrogen and carbon metabolic regulatory networks in Bacillus subtilis
inferred← citeshttps://doi.org/10.1016/j.ymben.2018.11.004openalex-snapshot
Systematically engineering the biosynthesis of a green biosurfactant surfactin by Bacillus subtilis 168
inferred← citeshttps://doi.org/10.1016/j.ymben.2025.06.003openalex-snapshot
High glutamate demand enables simultaneous consumption of glycerol and citrate despite carbon catabolite repression in engineered Bacillus subtilis strains
inferred← citeshttps://doi.org/10.1021/ac900675kopenalex-snapshot
Metabolomic Profiling of Anionic Metabolites by Capillary Electrophoresis Mass Spectrometry
inferred← citeshttps://doi.org/10.1021/acs.jproteome.5b01089openalex-snapshot
Redox Imbalance Underlies the Fitness Defect Associated with Inactivation of the Pta-AckA Pathway inStaphylococcus aureus
inferred← citeshttps://doi.org/10.1021/acs.jproteome.9b00413openalex-snapshot
Vegetative Cell and Spore Proteomes of Clostridioides difficile Show Finite Differences and Reveal Potential Protein Markers
inferred← citeshttps://doi.org/10.1021/acs.nanolett.9b00996openalex-snapshot
Bacteria-Derived Biological Carbon Building Robust Li–S Batteries
inferred← citeshttps://doi.org/10.1021/acssynbio.7b00069openalex-snapshot
Developing a Genetically Encoded, Cross-Species Biosensor for Detecting Ammonium and Regulating Biosynthesis of Cyanophycin
inferred← citeshttps://doi.org/10.1021/acssynbio.9b00005openalex-snapshot
Metabolic Engineering of Main Transcription Factors in Carbon, Nitrogen, and Phosphorus Metabolisms for Enhanced Production of Bacitracin in Bacillus licheniformis
inferred← citeshttps://doi.org/10.1038/ja.2010.78openalex-snapshot
Carbon source regulation of antibiotic production
inferred← citeshttps://doi.org/10.1038/msb.2009.40openalex-snapshot
A single transcription factor regulates evolutionarily diverse but functionally linked metabolic pathways in response to nutrient availability
inferred← citeshttps://doi.org/10.1038/msb.2009.82openalex-snapshot
Shifts in growth strategies reflect tradeoffs in cellular economics
inferred← citeshttps://doi.org/10.1038/msb.2011.34openalex-snapshot
Economics of membrane occupancy and respiro‐fermentation
inferred← citeshttps://doi.org/10.1038/ncomms1137openalex-snapshot
Systems-wide temporal proteomic profiling in glucose-starved Bacillus subtilis
inferred← citeshttps://doi.org/10.1038/nrmicro2351openalex-snapshot
Carbon metabolism of intracellular bacterial pathogens and possible links to virulence
inferred← citeshttps://doi.org/10.1038/s41396-021-01042-5openalex-snapshot
Metabolic adaption to extracellular pyruvate triggers biofilm formation in Clostridioides difficile
inferred← citeshttps://doi.org/10.1038/s41522-019-0087-4openalex-snapshot
A microbiota-generated bile salt induces biofilm formation in Clostridium difficile
inferred← citeshttps://doi.org/10.1038/s41564-024-01850-3openalex-snapshot
A framework for understanding collective microbiome metabolism
inferred← citeshttps://doi.org/10.1038/s41598-017-05628-yopenalex-snapshot
Small RNA mediated repression of subtilisin production in Bacillus licheniformis
inferred← citeshttps://doi.org/10.1038/s41598-018-36439-4openalex-snapshot
Stimulatory effects of amino acids on γ-polyglutamic acid production by Bacillus subtilis
inferred← citeshttps://doi.org/10.1038/s41598-021-99552-xopenalex-snapshot
Functional and structural analysis of catabolite control protein C that responds to citrate
inferred← citeshttps://doi.org/10.1038/s41598-023-33918-1openalex-snapshot
Functional characterization of the phosphotransferase system in Parageobacillus thermoglucosidasius
inferred← citeshttps://doi.org/10.1038/s44259-025-00147-7openalex-snapshot
Proteomic and metabolomic responses of priority bacterial pathogens to subinhibitory concentration of antibiotics
inferred← citeshttps://doi.org/10.1038/srep19486openalex-snapshot
Prediction and characterization of protein-protein interaction network in Bacillus licheniformis WX-02
inferred← citeshttps://doi.org/10.1038/srep32442openalex-snapshot
A Multi-Serotype Approach Clarifies the Catabolite Control Protein A Regulon in the Major Human Pathogen Group A Streptococcus
inferred← citeshttps://doi.org/10.1039/c0mb00315hopenalex-snapshot
A metabolomics and proteomics study of the adaptation of Staphylococcus aureus to glucose starvation
inferred← citeshttps://doi.org/10.1039/c6ra06468jopenalex-snapshot
Ratiometric fluorescent pH-sensitive polymers for high-throughput monitoring of extracellular pH
inferred← citeshttps://doi.org/10.1042/etls20220092openalex-snapshot
Bacterial acetate metabolism and its influence on human epithelia.
inferred← citeshttps://doi.org/10.1053/j.gastro.2009.02.073openalex-snapshot
Clostridium difficile Infection Caused by the Epidemic BI/NAP1/027 Strain
inferred← citeshttps://doi.org/10.1055/s-0043-119076openalex-snapshot
Effect of Diabetes on the Assessment Role of 2-Oxoglutarate to the Severity of Chronic Heart Failure
inferred← citeshttps://doi.org/10.1073/pnas.0711767105openalex-snapshot
A direct link between carbohydrate utilization and virulence in the major human pathogen group A Streptococcus
inferred← citeshttps://doi.org/10.1073/pnas.1300428110openalex-snapshot
Genome-wide identification of Bacillus subtilis CodY-binding sites at single-nucleotide resolution
inferred← citeshttps://doi.org/10.1073/pnas.1321308111openalex-snapshot
Hierarchical expression of genes controlled by the Bacillus subtilis global regulatory protein CodY
inferred← citeshttps://doi.org/10.1073/pnas.2025854118openalex-snapshot
An alternative resource allocation strategy in the chemolithoautotrophic archaeon Methanococcus maripaludis
inferred← citeshttps://doi.org/10.1074/jbc.m110.152843openalex-snapshot
Using NMR Metabolomics to Investigate Tricarboxylic Acid Cycle-dependent Signal Transduction in Staphylococcus epidermidis
inferred← citeshttps://doi.org/10.1074/jbc.m112.366492openalex-snapshot
13C-flux Analysis Reveals NADPH-balancing Transhydrogenation Cycles in Stationary Phase of Nitrogen-starving Bacillus subtilis
inferred← citeshttps://doi.org/10.1074/jbc.m112.418913openalex-snapshot
A Novel Mode of Regulation of the Staphylococcus aureus Catabolite Control Protein A (CcpA) Mediated by Stk1 Protein Phosphorylation
inferred← citeshttps://doi.org/10.1074/jbc.m114.562066openalex-snapshot
Control of the Diadenylate Cyclase CdaS in Bacillus subtilis
inferred← citeshttps://doi.org/10.1074/jbc.m114.592873openalex-snapshot
Multiple Regulatory Mechanisms Control the Expression of the Geobacillus stearothermophilus Gene for Extracellular Xylanase
inferred← citeshttps://doi.org/10.1074/jbc.m805951200openalex-snapshot
The CymR Regulator in Complex with the Enzyme CysK Controls Cysteine Metabolism in Bacillus subtilis
inferred← citeshttps://doi.org/10.1080/09712119.2015.1091346openalex-snapshot
Correlation between genomic analyses with metatranscriptomic study reveals various functional pathways ofClostridium sartagoformeAAU1, a buffalo rumen isolate
inferred← citeshttps://doi.org/10.1089/ars.2017.7335openalex-snapshot
Role of Proline in Pathogen and Host Interactions
inferred← citeshttps://doi.org/10.1093/femsle/fny248openalex-snapshot
Expression dynamics of the poly-γ-glutamic acid biosynthesis genes of Bacillus subtilis in response to glucose and glutamic acid-A pilot study
inferred← citeshttps://doi.org/10.1093/femspd/ftx005openalex-snapshot
Staphylococcus aureus pathogenesis in diverse host environments
inferred← citeshttps://doi.org/10.1093/femsre/fuag029openalex-snapshot
Feeding the invaders: how metabolic imbalance shapes infection and biofilm development
inferred← citeshttps://doi.org/10.1093/femsre/fuw013openalex-snapshot
Cyclic diguanylate signaling in Gram-positive bacteria
inferred← citeshttps://doi.org/10.1093/femsre/fux033openalex-snapshot
Glycerol metabolism and its implication in virulence in Mycoplasma
inferred← citeshttps://doi.org/10.1093/intbio/zyac010openalex-snapshot
Comparative biological network analysis for differentially expressed proteins as a function of bacilysin biosynthesis in Bacillus subtilis
inferred← citeshttps://doi.org/10.1093/jambio/lxad077openalex-snapshot
Non-redundant functionality of Lactiplantibacillus plantarum phospho-β-glucosidases revealed by carbohydrate utilization signatures associated to pbg2 and pbg4 gene mutants
inferred← citeshttps://doi.org/10.1093/jambio/lxad319openalex-snapshot
Transcriptome analysis reveals the underlying mechanism for over-accumulation of alkaline protease in Bacillus licheniformis
inferred← citeshttps://doi.org/10.1093/nar/gkad859openalex-snapshot
Design of a sorbitol-activated nitrogen metabolism-dependent regulatory system for redirection of carbon metabolism flow in Bacillus licheniformis
inferred← citeshttps://doi.org/10.1093/nar/gkn015openalex-snapshot
From one amino acid to another: tRNA-dependent amino acid biosynthesis
inferred← citeshttps://doi.org/10.1093/nar/gkp1085openalex-snapshot
Genome-wide gene regulation of biosynthesis and energy generation by a novel transcriptional repressor in Geobacter species
inferred← citeshttps://doi.org/10.1093/nar/gkp162openalex-snapshot
Phosphate control over nitrogen metabolism in Streptomyces coelicolor: direct and indirect negative control of glnR, glnA, glnII and amtB expression by the response regulator PhoP
inferred← citeshttps://doi.org/10.1093/nar/gkw775openalex-snapshot
The structure of the pleiotropic transcription regulator CodY provides insight into its GTP-sensing mechanism
inferred← citeshttps://doi.org/10.1099/mic.0.000744openalex-snapshot
Regulation of cid and lrg expression by CcpA in Streptococcus mutans
inferred← citeshttps://doi.org/10.1099/mic.0.001455openalex-snapshot
A historical sequence deletion in a commonly used Bacillus subtilis chromosome integration vector generates undetected loss-of-function mutations
inferred← citeshttps://doi.org/10.1099/mic.0.027839-0openalex-snapshot
From a consortium sequence to a unified sequence: the Bacillus subtilis 168 reference genome a decade later
inferred← citeshttps://doi.org/10.1099/mic.0.040667-0openalex-snapshot
l-Glutamine as a nitrogen source for Corynebacterium glutamicum: derepression of the AmtR regulon and implications for nitrogen sensing
inferred← citeshttps://doi.org/10.1099/mic.0.046417-0openalex-snapshot
Role of glucose and CcpA in capsule expression and virulence of Streptococcus suis
inferred← citeshttps://doi.org/10.1099/mic.0.051243-0openalex-snapshot
CcpA coordinates central metabolism and biofilm formation in Staphylococcus epidermidis
inferred← citeshttps://doi.org/10.1099/mic.0.060236-0openalex-snapshot
Global transcriptional analysis of the stringent response in Enterococcus faecalis
inferred← citeshttps://doi.org/10.1099/mic.0.063388-0openalex-snapshot
Dual role of CcpC protein in regulation of aconitase gene expression in Listeria monocytogenes and Bacillus subtilis
inferred← citeshttps://doi.org/10.1099/mic.0.071233-0openalex-snapshot
Regulation of the Bacillus subtilis mannitol utilization genes: promoter structure and transcriptional activation by the wild-type regulator (MtlR) and its mutants
inferred← citeshttps://doi.org/10.1099/mic.0.2008/019778-0openalex-snapshot
Induction of toxins in Clostridium difficile is associated with dramatic changes of its metabolism
inferred← citeshttps://doi.org/10.1101/2020.03.22.002139openalex-snapshot
A shared alarmone-GTP switch underlies triggered and spontaneous persistence
inferred← citeshttps://doi.org/10.1101/2023.04.14.536918openalex-snapshot
Differentiating Bacillus subtilis incorporates valine and methionine carbon into the backbone of specific fatty acids
inferred← citeshttps://doi.org/10.1101/2023.11.10.566560openalex-snapshot
Metabolic rewiring compensates for the loss of glutamate and aspartate biosynthesis in Bacillus subtilis
inferred← citeshttps://doi.org/10.1101/2024.03.20.585991openalex-snapshot
MOB rules: Antibiotic Exposure Reprograms Metabolism to Mobilize Bacillus subtilis in Competitive Interactions
inferred← citeshttps://doi.org/10.1101/2024.05.01.592088openalex-snapshot
KipOTIA detoxifies 5-oxoproline and promotes the growth of Clostridioides difficile
inferred← citeshttps://doi.org/10.1101/2025.06.29.661413openalex-snapshot
Non-cognate Phosphorylation of PhoP by YycG Links Carbon Catabolite Repression to Phosphate Starvation Response
inferred← citeshttps://doi.org/10.1101/2025.11.06.687015openalex-snapshot
Naturally occurring CodY variants alter ligand binding, DNA target affinity, and virulence in Clostridioides difficile
inferred← citeshttps://doi.org/10.1101/598045openalex-snapshot
Vegetative Cell and Spore Proteomes of Clostridioides difficile show finite differences and reveal potential biomarkers.
inferred← citeshttps://doi.org/10.1111/1462-2920.12676openalex-snapshot
Physiological and cell morphology adaptation of B acillus subtilis at near‐zero specific growth rates: a transcriptome analysis
inferred← citeshttps://doi.org/10.1111/1462-2920.12813openalex-snapshot
Evidence for synergistic control of glutamate biosynthesis by glutamate dehydrogenases and glutamate in B acillus subtilis
inferred← citeshttps://doi.org/10.1111/1462-2920.13454openalex-snapshot
YsbA and LytST are essential for pyruvate utilization in Bacillus subtilis
inferred← citeshttps://doi.org/10.1111/1541-4337.12565openalex-snapshot
Effectiveness of probiotics, prebiotics, and prebiotic‐like components in common functional foods
inferred← citeshttps://doi.org/10.1111/1541-4337.12785openalex-snapshot
Bacillus cereus food intoxication and toxicoinfection
inferred← citeshttps://doi.org/10.1111/1574-6968.12499openalex-snapshot
Initiation of sporulation inClostridium difficile: a twist on the classic model
inferred← citeshttps://doi.org/10.1111/1751-7915.14429openalex-snapshot
Metabolic rewiring enables ammonium assimilation via a non‐canonical fumarate‐based pathway
inferred← citeshttps://doi.org/10.1111/1751-7915.70026openalex-snapshot
Production‐optimized fermentation of antifungal compounds by Bacillus velezensis LZN01 and transcriptome analysis
inferred← citeshttps://doi.org/10.1111/1758-2229.12531openalex-snapshot
Hierarchical mutational events compensate for glutamate auxotrophy of a B acillus subtilis gltC mutant
inferred← citeshttps://doi.org/10.1111/j.1365-2958.2008.06290.xopenalex-snapshot
Molecular characterization of group A Streptococcus maltodextrin catabolism and its role in pharyngitis
inferred← citeshttps://doi.org/10.1111/j.1365-2958.2008.06369.xopenalex-snapshot
SlrR/SlrA controls the initiation of biofilm formation in Bacillus subtilis
inferred← citeshttps://doi.org/10.1111/j.1365-2958.2008.06568.xopenalex-snapshot
Genome‐wide responses to carbonyl electrophiles in Bacillus subtilis: control of the thiol‐dependent formaldehyde dehydrogenase AdhA and cysteine proteinase YraA by the MerR‐family regulator YraB (AdhR)
inferred← citeshttps://doi.org/10.1111/j.1365-2958.2009.06669.xopenalex-snapshot
Roles of relSpn in stringent response, global regulation and virulence of serotype 2 Streptococcus pneumoniae D39
inferred← citeshttps://doi.org/10.1111/j.1365-2958.2010.07339.xopenalex-snapshot
The global nutritional regulator CodY is an essential protein in the human pathogen Streptococcus pneumoniae
inferred← citeshttps://doi.org/10.1111/j.1365-2958.2010.07495.xopenalex-snapshot
CcpA‐mediated repression of Clostridium difficile toxin gene expression
inferred← citeshttps://doi.org/10.1111/j.1365-2958.2011.07692.xopenalex-snapshot
Mutational analysis of glucose transport regulation and glucose‐mediated virulence gene repression in Listeria monocytogenes
inferred← citeshttps://doi.org/10.1111/j.1365-2958.2011.07708.xopenalex-snapshot
Niche‐specific contribution to streptococcal virulence of a MalR‐regulated carbohydrate binding protein
inferred← citeshttps://doi.org/10.1111/j.1365-2958.2012.08090.xopenalex-snapshot
CodY orchestrates the expression of virulence determinants in emetic Bacillus cereus by impacting key regulatory circuits
inferred← citeshttps://doi.org/10.1111/j.1365-2958.2012.08105.xopenalex-snapshot
Control of glutamate homeostasis in Bacillus subtilis: a complex interplay between ammonium assimilation, glutamate biosynthesis and degradation
inferred← citeshttps://doi.org/10.1111/j.1420-9101.2007.01480.xopenalex-snapshot
Mechanisms of pathogenesis and the evolution of parasite virulence
inferred← citeshttps://doi.org/10.1111/j.1462-2920.2012.02766.xopenalex-snapshot
CodY, a pleiotropic regulator, influences multicellular behaviour and efficient production of virulence factors in Bacillus cereus
inferred← citeshttps://doi.org/10.1111/j.1574-6968.2009.01754.xopenalex-snapshot
Search for additional targets of the transcriptional regulator CcpN fromBacillus subtilis
inferred← citeshttps://doi.org/10.1111/j.1574-6976.2009.00199.xopenalex-snapshot
Extracellular signals that define distinct and coexisting cell fates inBacillus subtilis
inferred← citeshttps://doi.org/10.1111/j.1574-6976.2010.00216.xopenalex-snapshot
Common patterns – unique features: nitrogen metabolism and regulation in Gram-positive bacteria
inferred← citeshttps://doi.org/10.1111/j.1574-6976.2012.00351.xopenalex-snapshot
PIIsignal transduction proteins: nitrogen regulation and beyond
inferred← citeshttps://doi.org/10.1111/j.1742-4658.2012.08604.xopenalex-snapshot
CcpA forms complexes with CodY and RpoA in Bacillus subtilis
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