The mechanisms of carbon catabolite repression in bacteria

How Phosphotransferase System-Related Protein Phosphorylation Regulates Carbohydrate Metabolism in Bacteria

Deutscher, J., Francke, C., & Postma, P. W. (2006) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00024-06 · Cited by 1,411 · see citing works

Impact of Global Transcriptional Regulation by ArcA, ArcB, Cra, Crp, Cya, Fnr, and Mlc on Glucose Catabolism in Escherichia coli

Perrenoud, A., & Sauer, U. (2005) · Journal of Bacteriology · doi:10.1128/jb.187.9.3171-3179.2005 · Cited by 281 · see citing works

Mechanism responsible for glucose–lactose diauxie in Escherichia coli: challenge to the cAMP model

Inada, T., Kimata, K., & Aiba, H. (1996) · Genes to Cells · doi:10.1046/j.1365-2443.1996.24025.x · Cited by 203 · see citing works

The cyclic AMP receptor protein modulates quorum sensing, motility and multiple genes that affect intestinal colonization in Vibrio cholerae

Liang, W., Pascual-Montano, A., Silva, A. J., & Benítez, J. A. (2007) · Microbiology · doi:10.1099/mic.0.2007/006668-0 · Cited by 172 · see citing works

Correlation between Growth Rates, EIIA ^Crr Phosphorylation, and Intracellular Cyclic AMP Levels in <i>Escherichia coli</i> K-12

Bettenbrock, K., Sauter, T., Jahreis, K., Kremling, A., Lengeler, J. W., & Gilles, E.-D. (2007) · Journal of Bacteriology · doi:10.1128/jb.00819-07 · Cited by 171 · see citing works

Structural Basis for Allosteric Control of the Transcription Regulator CcpA by the Phosphoprotein HPr-Ser46-P

Schumacher, M. A., Allen, G. S., Diel, M., Seidel, G., Hillen, W., & Brennan, R. G. (2004) · Cell · doi:10.1016/j.cell.2004.08.027 · Cited by 170 · see citing works

Time-Resolved Determination of the CcpA Regulon of Lactococcus lactis subsp. cremoris MG1363

Zomer, A., Buist, G., Larsen, R., Kok, J., & Kuipers, O. P. (2007) · Journal of Bacteriology · doi:10.1128/jb.01013-06 · Cited by 156 · see citing works

The Pseudomonas putida Crc Global Regulator Controls the Expression of Genes from Several Chromosomal Catabolic Pathways for Aromatic Compounds

Morales, G., Linares, J. F., Beloso, A., Albar, J. P., Martínez, J. L., & Rojo, F. (2004) · Journal of Bacteriology · doi:10.1128/jb.186.5.1337-1344.2004 · Cited by 134 · see citing works

In Vitro Reconstitution of Catabolite Repression in Escherichia coli

Park, Y., Lee, B. R., Seok, Y., & Peterkofsky, A. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m512672200 · Cited by 125 · see citing works

The Pseudomonas putida Crc global regulator is an RNA binding protein that inhibits translation of the AlkS transcriptional regulator

Moreno, R., Manzano, A. R., Yuste, L., & Rojo, F. (2007) · Molecular Microbiology · doi:10.1111/j.1365-2958.2007.05685.x · Cited by 113 · see citing works

CcpC, a novel regulator of the LysR family required for glucose repression of the citB gene in Bacillus subtilis

Jourlin‐Castelli, C., Mani, N., NAKANO, M. M., & Sonenshein, A. L. (2000) · Journal of Molecular Biology · doi:10.1006/jmbi.1999.3420 · Cited by 108 · see citing works

Interference of Components of the Phosphoenolpyruvate Phosphotransferase System with the Central Virulence Gene Regulator PrfA ofListeria monocytogenes

Mertins, S., Joseph, B., Goetz, M., Ecke, R., Seidel, G., Sprehe, M., Hillen, W., Goebel, W., & Müller‐Altrock, S. (2006) · Journal of Bacteriology · doi:10.1128/jb.00972-06 · Cited by 105 · see citing works

Sugar Transport Systems of Bifidobacterium longum NCC2705

Parche, S., Amon, J., Janković, I., Rezzonico, E., Beleut, M., Barutçu, H., Schendel, I., Eddy, M. P., Burkovski, A., Arigoni, F., et al. (2006) · Microbial Physiology · doi:10.1159/000096455 · Cited by 103 · see citing works

Mutations lowering the phosphatase activity of HPr kinase/phosphatase switch off carbon metabolism

Monedero, V., Poncet, S., Mijakovic̀, I., Fieulaine, S., Dossonnet, V., Martin‐Verstraete, I., Nessler, S., & Deutscher, J. (2001) · The EMBO Journal · doi:10.1093/emboj/20.15.3928 · Cited by 103 · see citing works

The Target for the Pseudomonas putida Crc Global Regulator in the Benzoate Degradation Pathway Is the BenR Transcriptional Regulator

Moreno, R., & Rojo, F. (2007) · Journal of Bacteriology · doi:10.1128/jb.01604-07 · Cited by 92 · see citing works

The Novel Transcription Factor SgrR Coordinates the Response to Glucose-Phosphate Stress

Vanderpool, C. K., & Gottesman, S. (2007) · Journal of Bacteriology · doi:10.1128/jb.01689-06 · Cited by 90 · see citing works

The Phosphotransferase System Formed by PtsP, PtsO, and PtsN Proteins Controls Production of Polyhydroxyalkanoates in Pseudomonas putida

Velázquez, F., Pflüger, K., Cases, I., de Eugenio, L. I., & de Lorenzo, V. (2007) · Journal of Bacteriology · doi:10.1128/jb.00033-07 · Cited by 88 · see citing works

Identification and Characterization of a Fructose Phosphotransferase System in Bifidobacterium breve UCC2003

Mazé, A., Motherway, M. O., Fitzgerald, G. F., Deutscher, J., & van Sinderen, D. (2006) · Applied and Environmental Microbiology · doi:10.1128/aem.01496-06 · Cited by 86 · see citing works

CcpN (YqzB), a novel regulator for CcpA‐independent catabolite repression of Bacillus subtilis gluconeogenic genes

Servant, P., Coq, D. L., & Aymerich, S. (2005) · Molecular Microbiology · doi:10.1111/j.1365-2958.2005.04473.x · Cited by 85 · see citing works

The Catabolite Control Protein CcpA Binds to P mga and Influences Expression of the Virulence Regulator Mga in the Group A Streptococcus

Almengor, A. C., Kinkel, T. L., Day, S. J., & McIver, K. S. (2007) · Journal of Bacteriology · doi:10.1128/jb.01038-07 · Cited by 85 · see citing works

Integration of Signals through Crc and PtsN in Catabolite Repression of Pseudomonas putida TOL Plasmid pWW0

Aranda‐Olmedo, I., Ramos, J. L., & Marqués, S. (2005) · Applied and Environmental Microbiology · doi:10.1128/aem.71.8.4191-4198.2005 · Cited by 85 · see citing works

Implication of CcpN in the regulation of a novel untranslated RNA (SR1) in Bacillus subtilis

Licht, A., Preis, S., & Brantl, S. (2005) · Molecular Microbiology · doi:10.1111/j.1365-2958.2005.04810.x · Cited by 82 · see citing works

Structural Mechanism for the Fine-tuning of CcpA Function by The Small Molecule Effectors Glucose 6-Phosphate and Fructose 1,6-Bisphosphate

Schumacher, M. A., Seidel, G., Hillen, W., & Brennan, R. G. (2007) · Journal of Molecular Biology · doi:10.1016/j.jmb.2007.02.054 · Cited by 76 · see citing works

Activation of the LicT Transcriptional Antiterminator Involves a Domain Swing/Lock Mechanism Provoking Massive Structural Changes

Graille, M., Zhou, C., Receveur‐Brechot, V., Collinet, B., Declerck, N., & TILBEURGH, H. V. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m414642200 · Cited by 74 · see citing works

The Phosphotransferase System of Lactobacillus casei: Regulation of Carbon Metabolism and Connection to Cold Shock Response

Monedero, V., Mazé, A., Boël, G., Zúñiga, M., Beaufils, S., Hartke, A., & Deutscher, J. (2006) · Microbial Physiology · doi:10.1159/000096456 · Cited by 69 · see citing works

How Seryl-Phosphorylated HPr Inhibits PrfA, a Transcription Activator of Listeria monocytogenes Virulence Genes

Herro, R., Poncet, S., Cossart, P., Buchrieser, C., Gouin, E., Glaser, P., & Deutscher, J. (2005) · Microbial Physiology · doi:10.1159/000089650 · Cited by 66 · see citing works

Maltose transport in Lactobacillus casei and its regulation by inducer exclusion

Monedero, V., Yebra, M. J., Poncet, S., & Deutscher, J. (2007) · Research in Microbiology · doi:10.1016/j.resmic.2007.10.002 · Cited by 62 · see citing works

A New Piece of an Old Jigsaw: Glucose Kinase Is Activated Posttranslationally in a Glucose Transport-Dependent Manner in Streptomyces coelicolor A3(2)

van Wezel, G. P., König, M., Mahr, K., Nothaft, H., Thomae, A. W., Bibb, M. J., & Titgemeyer, F. (2006) · Microbial Physiology · doi:10.1159/000096461 · Cited by 59 · see citing works

Identification of a response regulator gene for catabolite control from a PCB‐degrading β‐proteobacteria, Acidovorax sp. KKS102

Ohtsubo, Y., Goto, H., Nagata, Y., Kudo, T., & Tsuda, M. (2006) · Molecular Microbiology · doi:10.1111/j.1365-2958.2006.05197.x · Cited by 56 · see citing works

CcpB, a Novel Transcription Factor Implicated in Catabolite Repression in Bacillus subtilis

Chauvaux, S., Paulsen, I. T., & Saier, M. H. (1998) · Journal of Bacteriology · doi:10.1128/jb.180.3.491-497.1998 · Cited by 55 · see citing works

Carbon Catabolite Repression of Type IV Pilus-Dependent Gliding Motility in the Anaerobic Pathogen Clostridium perfringens

Méndez, M. B., Huang, I., Ohtani, K., Grau, R. R., Shimizu, T., & Sarker, M. R. (2007) · Journal of Bacteriology · doi:10.1128/jb.01407-07 · Cited by 48 · see citing works

Regulatory Protein Phosphorylation in Mycoplasma pneumoniae

Halbedel, S., Busse, J., Schmidl, S. R., & Stülke, J. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m605010200 · Cited by 46 · see citing works

Role of the ptsN Gene Product in Catabolite Repression of the Pseudomonas putida TOL Toluene Degradation Pathway in Chemostat Cultures ▿

Aranda‐Olmedo, I., Marín, P., Ramos, J. L., & Marqués, S. (2006) · Applied and Environmental Microbiology · doi:10.1128/aem.01067-06 · Cited by 45 · see citing works

Phosphoprotein Crh-Ser46-P Displays Altered Binding to CcpA to Effect Carbon Catabolite Regulation

Schumacher, M. A., Seidel, G., Hillen, W., & Brennan, R. G. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m509977200 · Cited by 45 · see citing works

Regulation of citB expression in Bacillus subtilis: integration of multiple metabolic signals in the citrate pool and by the general nitrogen regulatory system

Blencke, H., Reif, I., Commichau, F. M., Detsch, C., Wacker, I., Ludwig, H., & Stülke, J. (2006) · Archives of Microbiology · doi:10.1007/s00203-005-0078-0 · Cited by 41 · see citing works

Growth-dependent Phosphorylation of the PtsN (EIINtr) Protein of Pseudomonas putida

Pflüger, K., & de Lorenzo, V. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m611110200 · Cited by 32 · see citing works

A protein-dependent riboswitch controlling ptsGHI operon expression in Bacillus subtilis: RNA structure rather than sequence provides interaction specificity

Schilling, O. (2004) · Nucleic Acids Research · doi:10.1093/nar/gkh611 · Cited by 31 · see citing works

Membrane localization itself but not binding to IICB Glc is directly responsible for the inactivation of the global repressor Mlc in Escherichia coli

Tanaka, Y., Itoh, F., Kimata, K., & Aiba, H. (2004) · Molecular Microbiology · doi:10.1111/j.1365-2958.2004.04179.x · Cited by 29 · see citing works

Keeping signals straight in transcription regulation: specificity determinants for the interaction of a family of conserved bacterial RNA–protein couples

Schilling, O., Herzberg, C., Hertrich, T., Vörsmann, H., Jessen, D., Hübner, S., Titgemeyer, F., & Stülke, J. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkl733 · Cited by 28 · see citing works

CcpC-Dependent Regulation of citB and lmo0847 in Listeria monocytogenes

Kim, H., Mittal, M., & Sonenshein, A. L. (2005) · Journal of Bacteriology · doi:10.1128/jb.188.1.179-190.2006 · Cited by 25 · see citing works

YeeI, a Novel Protein Involved in Modulation of the Activity of the Glucose-Phosphotransferase System in Escherichia coli K-12

Becker, A.-K., Zeppenfeld, T., Staab, A., Seitz, S., Boos, W., Morita, T., Aiba, H., Mahr, K., Titgemeyer, F., & Jahreis, K. (2006) · Journal of Bacteriology · doi:10.1128/jb.00219-06 · Cited by 25 · see citing works

Regulation of the mpt Operon in Listeria innocua by the ManR Protein

Xue, J., & Miller, K. W. (2007) · Applied and Environmental Microbiology · doi:10.1128/aem.00052-07 · Cited by 24 · see citing works

The Activity of the Lactose Transporter from Streptococcus thermophilus Is Increased by Phosphorylated IIA and the Action of β-Galactosidase

Geertsma, E. R., Duurkens, R. H., & Poolman, B. (2005) · Biochemistry · doi:10.1021/bi051638w · Cited by 23 · see citing works

Topography of the Surface of the Signal-transducing Protein EIIAGlc That Interacts with the MalK Subunits of the Maltose ATP-binding Cassette Transporter (MalFGK2) of Salmonella typhimurium

Blüschke, B., Volkmer, R., & Schneider, E. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m512646200 · Cited by 23 · see citing works

Carbon Catabolite Repression of Sucrose Utilization in Staphylococcus xylosus: Catabolite Control Protein CcpA Ensures Glucose Preference and Autoregulatory Limitation of Sucrose Utilization

Janković, I., & Brückner, R. (2006) · Microbial Physiology · doi:10.1159/000096466 · Cited by 22 · see citing works

Deduction of consensus binding sequences on proteins that bind IIA Glc of the phospho enol pyruvate:sugar phosphotransferase system by cysteine scanning mutagenesis of Escherichia coli lactose permease

Sondej, M. A., Sun, J., Seok, Y., Kaback, H. R., & Peterkofsky, A. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.7.3525 · Cited by 22 · see citing works

Control of the Phosphorylation State of the HPr Protein of the Phosphotransferase System in Bacillus subtilis: Implication of the Protein Phosphatase PrpC

Singh, K. D., Halbedel, S., Görke, B., & Stülke, J. (2007) · Microbial Physiology · doi:10.1159/000103608 · Cited by 20 · see citing works

CcpA Mutants with Differential Activities in Bacillus subtilis

Sprehe, M., Seidel, G., Diel, M., & Hillen, W. (2006) · Microbial Physiology · doi:10.1159/000096464 · Cited by 20 · see citing works

Structural Analysis of the Bacterial HPr Kinase/Phosphorylase V267F Mutant Gives Insights into the Allosteric Regulation Mechanism of This Bifunctional Enzyme

Chaptal, V., Vincent, F., Gueguen‐Chaignon, V., Monedero, V., Poncet, S., Deutscher, J., Nessler, S., & Moréra, S. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m705979200 · Cited by 17 · see citing works

Mlc of Thermus thermophilus : a Glucose-Specific Regulator for a Glucose/Mannose ABC Transporter in the Absence of the Phosphotransferase System

Chevance, F. F. V., Erhardt, M., Lengsfeld, C., Lee, S.-J., & Boos, W. (2006) · Journal of Bacteriology · doi:10.1128/jb.00715-06 · Cited by 14 · see citing works

Structural analysis of B. subtilis CcpA effector binding site

Chaptal, V., Gueguen‐Chaignon, V., Poncet, S., Lecampion, C., Meyer, P., Deutscher, J., Galinier, A., Nessler, S., & Moréra, S. (2006) · Proteins Structure Function and Bioinformatics · doi:10.1002/prot.21001 · Cited by 11 · see citing works

Structure of full-length transcription regulator CcpA in the apo form

Loll, B., Saenger, W., & Biesiadka, J. (2007) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2007.03.020 · Cited by 8 · see citing works

Carbon catabolite repression in bacteria: many ways to make the most out of nutrients

Görke, B., & Stülke, J. (2008) · Nature Reviews Microbiology · doi:10.1038/nrmicro1932 · Cited by 1,701 · see citing works

The Biology of Streptococcus mutans

Lemos, J. A. C., Palmer, S. R., Zeng, L., Wen, Z. T., Kajfasz, J. K., Freires, I. A., Abranches, J., & Brady, L. J. (2019) · Microbiology Spectrum · doi:10.1128/microbiolspec.gpp3-0051-2018 · Cited by 933 · see citing works

Degradation of alkanes by bacteria

Rojo, F. (2009) · Environmental Microbiology · doi:10.1111/j.1462-2920.2009.01948.x · Cited by 824 · see citing works

The oral microbiome: Role of key organisms and complex networks in oral health and disease

Sedghi, L., DiMassa, V., Harrington, A., Lynch, S. V., & Kapila, Y. L. (2021) · Periodontology 2000 · doi:10.1111/prd.12393 · Cited by 755 · see citing works

Engineered reversal of the β-oxidation cycle for the synthesis of fuels and chemicals

Dellomonaco, C., Clomburg, J. M., Miller, E. N., & González, R. (2011) · Nature · doi:10.1038/nature10333 · Cited by 597 · see citing works

Biology of Oral Streptococci

Abranches, J., Zeng, L., Kajfasz, J. K., Palmer, S. R., Chakraborty, B., Wen, Z. T., Richards, V. P., Brady, L. J., & Lemos, J. A. C. (2018) · Microbiology Spectrum · doi:10.1128/microbiolspec.gpp3-0042-2018 · Cited by 558 · see citing works

Carbon catabolite repression in Pseudomonas : optimizing metabolic versatility and interactions with the environment

Rojo, F. (2010) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2010.00218.x · Cited by 545 · see citing works

The Bacterial Phosphoenolpyruvate:Carbohydrate Phosphotransferase System: Regulation by Protein Phosphorylation and Phosphorylation-Dependent Protein-Protein Interactions

Deutscher, J., Aké, F. M., Derkaoui, M., Zébré, A. C., Cao, T. N., Bouraoui, H., Kentache, T., Mokhtari, A., Milohanic, E., & Joyet, P. (2014) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00001-14 · Cited by 432 · see citing works

Production of microbial secondary metabolites: Regulation by the carbon source

Ruiz‐Villafán, B., Chávez, A., Forero, A. V. F., García-Huante, Y., Romero, A., Sánchez, M., Rocha-Mendoza, D., Sánchez, B., Rodrı́guez-Sanoja, R., Sánchez, S., et al. (2010) · Critical Reviews in Microbiology · doi:10.3109/10408410903489576 · Cited by 384 · see citing works

Signal beyond nutrient, fructose, exuded by an arbuscular mycorrhizal fungus triggers phytate mineralization by a phosphate solubilizing bacterium

Zhang, L., Feng, G., & Declerck, S. (2018) · The ISME Journal · doi:10.1038/s41396-018-0171-4 · Cited by 311 · see citing works

Regulation of Listeria virulence: PrfA master and commander

Heras, A. D. L., Cain, R. J., Bielecka, M. K., & Vázquez‐Boland, J. A. (2011) · Current Opinion in Microbiology · doi:10.1016/j.mib.2011.01.005 · Cited by 299 · see citing works

Carbon source regulation of antibiotic production

Sánchez, S., Chávez, A., Forero, A. V. F., García-Huante, Y., Romero, A., Sánchez, M., Rocha-Mendoza, D., Sánchez, B., Ávalos, M., Guzmán‐Trampe, S., et al. (2010) · The Journal of Antibiotics · doi:10.1038/ja.2010.78 · Cited by 297 · see citing works

Biodegradable and conventional microplastics exhibit distinct microbiome, functionality, and metabolome changes in soil

Sun, Y., Duan, C., Cao, N., Ding, C., Huang, Y., & Wang, J. (2021) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2021.127282 · Cited by 280 · see citing works

Novel Roles of cAMP Receptor Protein (CRP) in Regulation of Transport and Metabolism of Carbon Sources

Shimada, T., Fujita, N., Yamamoto, K., & Ishihama, A. (2011) · PLoS ONE · doi:10.1371/journal.pone.0020081 · Cited by 265 · see citing works

Growth strategy of microbes on mixed carbon sources

Wang, X., Xia, K., Yang, X., & Tang, C. (2019) · Nature Communications · doi:10.1038/s41467-019-09261-3 · Cited by 242 · see citing works

The CRE1 carbon catabolite repressor of the fungus Trichoderma reesei: a master regulator of carbon assimilation

Portnoy, T., Margeot, A., Linke, R. B., Atanasova, L., Fekete, E., Sándor, E., Hartl, L., Karaffa, L., Druzhinina, I. S., Seiboth, B., et al. (2011) · BMC Genomics · doi:10.1186/1471-2164-12-269 · Cited by 233 · see citing works

Metabolic crosstalk between host and pathogen: sensing, adapting and competing

Olive, A. J., & Sassetti, C. M. (2016) · Nature Reviews Microbiology · doi:10.1038/nrmicro.2016.12 · Cited by 228 · see citing works

Hydrogen from food processing wastes via photofermentation using Purple Non-sulfur Bacteria (PNSB)—A review

Ghosh, S., Dairkee, U. K., Chowdhury, R., & Bhattacharya, P. (2017) · Energy Conversion and Management · doi:10.1016/j.enconman.2016.09.001 · Cited by 189 · see citing works

Starter Cultures: General Aspects

Parente, E., Cogan, T. M., & Powell, I. B. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-417012-4.00008-9 · Cited by 186 · see citing works

Consolidated bio-saccharification: Leading lignocellulose bioconversion into the real world

Liu, Y., Li, B., Feng, Y., & Cui, Q. (2020) · Biotechnology Advances · doi:10.1016/j.biotechadv.2020.107535 · Cited by 183 · see citing works

Genetic Architecture of Intrinsic Antibiotic Susceptibility

Girgis, H. S., Hottes, A. K., & Tavazoie, S. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005629 · Cited by 178 · see citing works

A Functional Genomics Approach to Establish the Complement of Carbohydrate Transporters in Streptococcus pneumoniae

Bidossi, A., Mulas, L., Decorosi, F., Colomba, L., Ricci, S., Pozzi, G., Deutscher, J., Viti, C., & Oggioni, M. (2012) · PLoS ONE · doi:10.1371/journal.pone.0033320 · Cited by 179 · see citing works

The Pore-Forming Haemolysins of Bacillus Cereus: A Review

Ramarao, N., & Sanchis, V. (2013) · Toxins · doi:10.3390/toxins5061119 · Cited by 171 · see citing works

Genomic and functional analysis of Romboutsia ilealis CRIB T reveals adaptation to the small intestine

Gerritsen, J., Hornung, B., Renckens, B. A. M., van Hijum, S. A. F. T., dos Santos, V. A. P. M., Rijkers, G. T., Schaap, P. J., de Vos, W. M., & Smidt, H. (2017) · PeerJ · doi:10.7717/peerj.3698 · Cited by 171 · see citing works

Regulation of Arabinose and Xylose Metabolism in Escherichia coli

Desai, T. A., & Rao, C. V. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.01970-09 · Cited by 170 · see citing works

Effect of a glucose impulse on the CcpA regulon in Staphylococcus aureus

Seidl, K., Müller, S., François, P., Kriebitzsch, C., Schrenzel, J., Engelmann, S., Bischoff, M., & Berger‐Bächi, B. (2009) · BMC Microbiology · doi:10.1186/1471-2180-9-95 · Cited by 165 · see citing works

Fueling the caries process: carbohydrate metabolism and gene regulation by<i>Streptococcus mutans</i>

Moye, Z. D., Zeng, L., & Burne, R. A. (2014) · Journal of Oral Microbiology · doi:10.3402/jom.v6.24878 · Cited by 164 · see citing works

Adaptive Evolution of<i>Escherichia coli</i>K-12 MG1655 during Growth on a Nonnative Carbon Source,<scp>l</scp>-1,2-Propanediol

Lee, D.-H., & Palsson, B. Ø. (2010) · Applied and Environmental Microbiology · doi:10.1128/aem.00373-10 · Cited by 160 · see citing works

Biogenic ammonia modifies antibiotic resistance at a distance in physically separated bacteria

Bernier, S. P., Létoffé, S., Delepierre, M., & Ghigo, J. (2011) · Molecular Microbiology · doi:10.1111/j.1365-2958.2011.07724.x · Cited by 159 · see citing works

Regulatory roles of the bacterial nitrogen-related phosphotransferase system

Pflüger‐Grau, K., & Görke, B. (2010) · Trends in Microbiology · doi:10.1016/j.tim.2010.02.003 · Cited by 158 · see citing works

Carbon Catabolite Repression in Bacillus subtilis : Quantitative Analysis of Repression Exerted by Different Carbon Sources

Singh, K. D., Schmalisch, M. H., Stülke, J., & Görke, B. (2008) · Journal of Bacteriology · doi:10.1128/jb.00848-08 · Cited by 145 · see citing works

Sugar transporters in efficient utilization of mixed sugar substrates: current knowledge and outlook

Jojima, T., Omumasaba, C. A., Inui, M., & Yukawa, H. (2009) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-009-2292-1 · Cited by 144 · see citing works

Current knowledge of the Escherichia coli phosphoenolpyruvate–carbohydrate phosphotransferase system: peculiarities of regulation and impact on growth and product formation

Escalante, A., Cervantes, A. S., Gosset, G., & Bolívar, F. G. (2012) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-012-4101-5 · Cited by 142 · see citing works

Cultivation media for lactic acid bacteria used in dairy products

Hayek, S. A., Gyawali, R., Aljaloud, S. O., Krastanov, A. I., & Ibrahim, S. A. (2019) · Journal of Dairy Research · doi:10.1017/s002202991900075x · Cited by 141 · see citing works

Glycerol Metabolism Is Important for Cytotoxicity of Mycoplasma pneumoniae

Hames, C., Halbedel, S., Hoppert, M., Joachim Frey, A., & Stülke, J. (2008) · Journal of Bacteriology · doi:10.1128/jb.01103-08 · Cited by 138 · see citing works

The impact of carbon and nitrogen catabolite repression in microorganisms

Nair, A., & Sarma, S. J. (2021) · Microbiological Research · doi:10.1016/j.micres.2021.126831 · Cited by 134 · see citing works

Degradation and assimilation of aromatic compounds by Corynebacterium glutamicum: another potential for applications for this bacterium?

Shen, X., Zhou, N., & Liu, S. (2012) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-012-4139-4 · Cited by 133 · see citing works

Fermentation Inhibitors in Ethanol Processes and Different Strategies to Reduce Their Effects

Taherzadeh, M. J., & Karimi, K. (2011) · Elsevier eBooks · doi:10.1016/b978-0-12-385099-7.00012-7 · Cited by 131 · see citing works

Shaping bacterial gene expression by physiological and proteome allocation constraints

Scott, M., & Terence Hwa, B. (2022) · Nature Reviews Microbiology · doi:10.1038/s41579-022-00818-6 · Cited by 128 · see citing works

Isolation and screening of bacterial isolates from wastewater treatment plants to decolorize azo dyes

Meerbergen, K., Willems, K., Dewil, R., van Impe, J. F. M., Appels, L., & Lievens, B. (2017) · Journal of Bioscience and Bioengineering · doi:10.1016/j.jbiosc.2017.11.008 · Cited by 130 · see citing works

Biodegradation of Volatile Organic Compounds and Their Effects on Biodegradability under Co-Existing Conditions

Yoshikawa, M., Zhang, M., & Toyota, K. (2017) · Microbes and Environments · doi:10.1264/jsme2.me16188 · Cited by 123 · see citing works

Two small RNAs, CrcY and CrcZ, act in concert to sequester the Crc global regulator in Pseudomonas putida , modulating catabolite repression

Moreno, R., Fonseca, P., & Rojo, F. (2011) · Molecular Microbiology · doi:10.1111/j.1365-2958.2011.07912.x · Cited by 120 · see citing works

The transport and mediation mechanisms of the common sugars in Escherichia coli

Luo, Y., Zhang, T., & Wu, H. C. (2014) · Biotechnology Advances · doi:10.1016/j.biotechadv.2014.04.009 · Cited by 117 · see citing works

Relaxed control of sugar utilization in Lactobacillus brevis

Kim, J.-H., Shoemaker, S. P., & Mills, D. A. (2009) · Microbiology · doi:10.1099/mic.0.024653-0 · Cited by 114 · see citing works

Simultaneous utilization of glucose and xylose via novel mechanisms in engineered Escherichia coli

Kim, S. M., Choi, B. Y., Ryu, Y. S., Jung, S. H., Park, J. M., Kim, G.-H., & Lee, S. K. (2015) · Metabolic Engineering · doi:10.1016/j.ymben.2015.05.002 · Cited by 114 · see citing works

The Crc and Hfq proteins of P seudomonas putida cooperate in catabolite repression and formation of ribonucleic acid complexes with specific target motifs

Moreno, R., Hernández‐Arranz, S., Rosa, R. L., Yuste, L., Madhushani, A., Shingler, V., & Rojo, F. (2014) · Environmental Microbiology · doi:10.1111/1462-2920.12499 · Cited by 113 · see citing works

Carbon Catabolite Repression and Impranil Polyurethane Degradation in Pseudomonas protegens Strain Pf-5

Hung, C., Zingarelli, S., Nadeau, L. J., Biffinger, J. C., Drake, C. A., Crouch, A. L., Barlow, D. E., Russell, J. N., & Crookes‐Goodson, W. J. (2016) · Applied and Environmental Microbiology · doi:10.1128/aem.01448-16 · Cited by 112 · see citing works

Live and let die: Hydrogen peroxide production by the commensal flora and its role in maintaining a symbiotic microbiome

Redanz, S., Cheng, X., Giacaman, R. A., Pfeifer, C. S., Merritt, J. L., & Kreth, J. (2018) · Molecular Oral Microbiology · doi:10.1111/omi.12231 · Cited by 111 · see citing works

Utilization of Lactose and Galactose by Streptococcus mutans : Transport, Toxicity, and Carbon Catabolite Repression

Zeng, L., Das, S., & Burne, R. A. (2010) · Journal of Bacteriology · doi:10.1128/jb.01624-09 · Cited by 110 · see citing works

The lag-phase during diauxic growth is a trade-off between fast adaptation and high growth rate

Chu, D., & Barnes, D. J. (2016) · Scientific Reports · doi:10.1038/srep25191 · Cited by 109 · see citing works

Sophisticated Regulation of Transcriptional Factors by the Bacterial Phosphoenolpyruvate: Sugar Phosphotransferase System

Galinier, A., & Deutscher, J. (2017) · Journal of Molecular Biology · doi:10.1016/j.jmb.2017.02.006 · Cited by 109 · see citing works

Stimulation of the potassium sensor KdpD kinase activity by interaction with the phosphotransferase protein IIANtr in Escherichia coli

Lüttmann, D., Heermann, R., Zimmer, B., Hillmann, A., Rampp, I. S., Jung, K., & Görke, B. (2009) · Molecular Microbiology · doi:10.1111/j.1365-2958.2009.06704.x · Cited by 105 · see citing works

The major PEP-phosphotransferase systems (PTSs) for glucose, mannose and cellobiose of Listeria monocytogenes, and their significance for extra- and intracellular growth

Stoll, R., & Goebel, W. (2010) · Microbiology · doi:10.1099/mic.0.034934-0 · Cited by 105 · see citing works

Chitin colonization, chitin degradation and chitin‐induced natural competence of Vibrio cholerae are subject to catabolite repression

Blokesch, M. (2012) · Environmental Microbiology · doi:10.1111/j.1462-2920.2011.02689.x · Cited by 103 · see citing works

Glycerol metabolism and its implication in virulence in Mycoplasma

Blötz, C., & Stülke, J. (2017) · FEMS Microbiology Reviews · doi:10.1093/femsre/fux033 · Cited by 99 · see citing works

Noncoding RNA control of the making and breaking of sugarsPreprint

Görke, B., & Vogel, J. (2008) · Genes & Development · doi:10.1101/gad.1717808 · Cited by 103 · see citing works

Regulation of metabolism in Escherichia coli during growth on mixtures of the non-glucose sugars: arabinose, lactose, and xylose

Ammar, E. M., Wang, X., & Rao, C. V. (2018) · Scientific Reports · doi:10.1038/s41598-017-18704-0 · Cited by 101 · see citing works

The Crc global regulator binds to an unpaired A-rich motif at the Pseudomonas putida alkS mRNA coding sequence and inhibits translation initiation

Moreno, R., Marzi, S., Romby, P., & Rojo, F. (2009) · Nucleic Acids Research · doi:10.1093/nar/gkp825 · Cited by 100 · see citing works

Mucus Sugar Content Shapes the Bacterial Community Structure in Thermally Stressed Acropora muricata

Lee, S. T. M., Davy, S., Tang, S.-L., & Kench, P. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.00371 · Cited by 92 · see citing works

Rewiring carbon catabolite repression for microbial cell factory

Parisutham, V., Kim, M. K., Lee, S.-K., & Ghim, C.-M. (2012) · BMB Reports · doi:10.5483/bmbrep.2012.45.2.59 · Cited by 100 · see citing works

Self-Inducible Bacillus subtilis Expression System for Reliable and Inexpensive Protein Production by High-Cell-Density Fermentation

Wenzel, M., Müller, A., Siemann-Herzberg, M., & Altenbuchner, J. (2011) · Applied and Environmental Microbiology · doi:10.1128/aem.05219-11 · Cited by 100 · see citing works

Role of glucose and CcpA in capsule expression and virulence of Streptococcus suis

Willenborg, J., Fulde, M., de Greeff, A., Rohde, M., Smith, H. E., Valentin‐Weigand, P., & Goethe, R. (2011) · Microbiology · doi:10.1099/mic.0.046417-0 · Cited by 99 · see citing works

Dynamic metabolic adaptation can promote species coexistence in competitive microbial communities

Pacciani-Mori, L., Giometto, A., Suweis, S. S., & Maritan, A. (2020) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1007896 · Cited by 101 · see citing works

Physiological and biochemical characterization of the two α-l-rhamnosidases of Lactobacillus plantarum NCC245

Ávila, M., Jaquet, M., Moine, D., Requena, T., Peláez, C., Arigoni, F., & Janković, I. (2009) · Microbiology · doi:10.1099/mic.0.027789-0 · Cited by 98 · see citing works

Bacterial Responses to Glyoxal and Methylglyoxal: Reactive Electrophilic Species

Lee, C. D., & Park, C. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18010169 · Cited by 97 · see citing works

Recent advances of biofuels and biochemicals production from sustainable resources using co-cultivation systems

Jiang, Y., Wu, R., Zhou, J., He, A., Xu, J., Xin, F., Zhang, W., Ma, J., Jiang, M., & Dong, W. (2019) · Biotechnology for Biofuels · doi:10.1186/s13068-019-1495-7 · Cited by 93 · see citing works

The Maltose ABC Transporter in Lactococcus lactis Facilitates High-Level Sensitivity to the Circular Bacteriocin Garvicin ML

Gabrielsen, C., Brede, D. A., Hernández, P. E., Nes, I. F., & Diep, D. B. (2012) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00314-12 · Cited by 92 · see citing works

Fermentation and proteome profiles of Lactobacillus plantarum strains during growth under food-like conditions

Siragusa, S., Angelis, M. D., Calasso, M. P., Campanella, D., Minervini, F., Cagno, R. D., & Gobbetti, M. (2013) · Journal of Proteomics · doi:10.1016/j.jprot.2013.11.003 · Cited by 91 · see citing works

Multiple stable states in microbial communities explained by the stable marriage problem

Goyal, A., Dubinkina, V. B., & Maslov, S. (2018) · The ISME Journal · doi:10.1038/s41396-018-0222-x · Cited by 88 · see citing works

Fed-batch fermentation for enhanced lactic acid production from glucose/xylose mixture without carbon catabolite repression

Abdel‐Rahman, M. A., Yaotian, X., Tashiro, Y., Wang, Y., Zendo, T., Sakai, K., & Sonomoto, K. (2014) · Journal of Bioscience and Bioengineering · doi:10.1016/j.jbiosc.2014.07.007 · Cited by 88 · see citing works

Persister Cells Resuscitate Using Membrane Sensors that Activate Chemotaxis, Lower cAMP Levels, and Revive Ribosomes

Yamasaki, R., Song, S., Benedik, M. J., & Wood, T. K. (2019) · iScience · doi:10.1016/j.isci.2019.100792 · Cited by 86 · see citing works

Connecting Environment and Genome Plasticity in the Characterization of Transformation-Induced SOS Regulation and Carbon Catabolite Control of the Vibrio cholerae Integron Integrase

Baharoglu, Z., Krin, E., & Mazel, D. (2012) · Journal of Bacteriology · doi:10.1128/jb.05982-11 · Cited by 86 · see citing works

What bacteria want

Galperin, M. Y. (2018) · Environmental Microbiology · doi:10.1111/1462-2920.14398 · Cited by 84 · see citing works

Phosphoenolpyruvate phosphotransferase system regulates detection and processing of the quorum sensing signal autoinducer‐2

Pereira, C. S., Santos, A. J. M., Bejerano‐Sagie, M., Correia, P. B., Marques, J. C., & Xavier, K. B. (2012) · Molecular Microbiology · doi:10.1111/j.1365-2958.2012.08010.x · Cited by 82 · see citing works

The Variable Regions of Lactobacillus rhamnosus Genomes Reveal the Dynamic Evolution of Metabolic and Host-Adaptation Repertoires

Ceapă, C. D., Davids, M., Ritari, J., Lambert, J. M., Wels, M., Douillard, F. P., Smokvina, T., de Vos, W. M., Knol, J., & Kleerebezem, M. (2016) · Genome Biology and Evolution · doi:10.1093/gbe/evw123 · Cited by 77 · see citing works

Regulation of the Type I-F CRISPR-Cas system by CRP-cAMP and GalM controls spacer acquisition and interference

Patterson, A. G., Chang, J. T., Taylor, C., & Fineran, P. C. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv517 · Cited by 76 · see citing works

Class IIa bacteriocin resistance in Enterococcus faecalis V583: The mannose PTS operon mediates global transcriptional responses

Opsata, M., Nes, I. F., & Holo, H. (2010) · BMC Microbiology · doi:10.1186/1471-2180-10-224 · Cited by 76 · see citing works

Metabolic profile of ginkgo kernel juice fermented with lactic aicd bacteria: A potential way to degrade ginkgolic acids and enrich terpene lactones and phenolics

Wang, Y., Tao, Y., Zhang, X., Shao, S., Han, Y., Chu, D., Xie, G., & Ye, X. (2018) · Process Biochemistry · doi:10.1016/j.procbio.2018.11.006 · Cited by 74 · see citing works

Role of the cAMP-Dependent Carbon Catabolite Repression in Capsular Polysaccharide Biosynthesis in Klebsiella pneumoniae

Lin, C., Chen, Y., Jinn, T., Wu, C.-C., Hong, Y.-M., & Wu, W. (2013) · PLoS ONE · doi:10.1371/journal.pone.0054430 · Cited by 75 · see citing works

Surface Export of GAPDH/SDH, a Glycolytic Enzyme, Is Essential for Streptococcus pyogenes Virulence

Jin, H., Agarwal, S., Agarwal, S., & Pancholi, V. (2011) · mBio · doi:10.1128/mbio.00068-11 · Cited by 73 · see citing works

The CRISPR/Cas9-facilitated multiplex pathway optimization (CFPO) technique and its application to improve the Escherichia coli xylose utilization pathway

Zhu, X., Zhao, D., Qiu, H., Fan, F., Man, S., Bi, C., & Zhang, X. (2017) · Metabolic Engineering · doi:10.1016/j.ymben.2017.08.003 · Cited by 73 · see citing works

Microbial Utilization of Next-Generation Feedstocks for the Biomanufacturing of Value-Added Chemicals and Food Ingredients

Zhang, C., Ottenheim, C., Weingarten, M., & Ji, L. (2022) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2022.874612 · Cited by 72 · see citing works

Transcriptional Regulation of the Cellobiose Operon of Streptococcus mutans

Zeng, L., & Burne, R. A. (2009) · Journal of Bacteriology · doi:10.1128/jb.01641-08 · Cited by 72 · see citing works

GAPDH: Biological Properties and Diversity

Seidler, N. W. (2012) · Advances in experimental medicine and biology · doi:10.1007/978-94-007-4716-6 · Cited by 71 · see citing works

Maltose and Maltodextrin Utilization by Listeria monocytogenes Depend on an Inducible ABC Transporter which Is Repressed by Glucose

Gopal, S., Berg, D., Hagen, N., Schriefer, E.-M., Stoll, R., Goebel, W., & Kreft, J. (2010) · PLoS ONE · doi:10.1371/journal.pone.0010349 · Cited by 70 · see citing works

Gene Regulation by CcpA and Catabolite Repression Explored by RNA-Seq in Streptococcus mutans

Zeng, L., Choi, S. C., Danko, C. G., Siepel, A. C., Stanhope, M. J., & Burne, R. A. (2013) · PLoS ONE · doi:10.1371/journal.pone.0060465 · Cited by 69 · see citing works

Comparison of different Bacillus subtilis expression systems

Vavrová, Ľ., Muchová, K., & Barák, I. (2010) · Research in Microbiology · doi:10.1016/j.resmic.2010.09.004 · Cited by 67 · see citing works

Seryl‐phosphorylated HPr regulates CcpA‐independent carbon catabolite repression in conjunction with PTS permeases in Streptococcus mutans

Zeng, L., & Burne, R. A. (2010) · Molecular Microbiology · doi:10.1111/j.1365-2958.2009.07029.x · Cited by 67 · see citing works

The Crc Global Regulator Inhibits the Pseudomonas putida pWW0 Toluene/Xylene Assimilation Pathway by Repressing the Translation of Regulatory and Structural Genes

Moreno, R., Fonseca, P., & Rojo, F. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.126615 · Cited by 67 · see citing works

Post-translational modifications as key regulators of bacterial metabolic fluxes

Pisithkul, T., Patel, N. M., & Amador‐Noguez, D. (2015) · Current Opinion in Microbiology · doi:10.1016/j.mib.2014.12.006 · Cited by 66 · see citing works

Biohydrogen and poly-β-hydroxybutyrate production by winery wastewater photofermentation: Effect of substrate concentration and nitrogen source

Policastro, G., Luongo, V., & Fabbricino, M. (2020) · Journal of Environmental Management · doi:10.1016/j.jenvman.2020.111006 · Cited by 66 · see citing works

Bacterial cell envelope and extracellular sulfhydryl binding sites: Their roles in metal binding and bioavailability

Fein, J. B., Yu, Q., Nam, J., & Yee, N. (2019) · Chemical Geology · doi:10.1016/j.chemgeo.2019.04.026 · Cited by 65 · see citing works

The GlxR regulon of the amino acid producer Corynebacterium glutamicum: Detection of the corynebacterial core regulon and integration into the transcriptional regulatory network model

Kohl, T. A., & Tauch, A. (2009) · Journal of Biotechnology · doi:10.1016/j.jbiotec.2009.08.005 · Cited by 64 · see citing works

Effects of bioreactor hydrodynamics on the physiology of Streptomyces

Olmos, É., Mehmood, N., Husein, L. H., Goergen, J. L., Fick, M., & Delaunay, S. (2012) · Bioprocess and Biosystems Engineering · doi:10.1007/s00449-012-0794-1 · Cited by 64 · see citing works

Structures of carbon catabolite protein A–(HPr-Ser46-P) bound to diverse catabolite response element sites reveal the basis for high-affinity binding to degenerate DNA operators

Schumacher, M. A., Sprehe, M., Bartholomae, M., Hillen, W., & Brennan, R. G. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq1177 · Cited by 64 · see citing works

Microbial plastic degradation: enzymes, pathways, challenges, and perspectives

Pérez-García, P., Saß, K., Wongwattanarat, S., Amann, J., Feuerriegel, G., Neumann, T., Bäse, N., Schmitz, L. S., Dierkes, R. F., Gurschke, M., et al. (2025) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00087-24 · Cited by 69 · see citing works

Klebsiella pneumoniae l- Fucose Metabolism Promotes Gastrointestinal Colonization and Modulates Its Virulence Determinants

Hudson, A. W., Barnes, A. J., Bray, A. S., Ornelles, D. A., & Zafar, M. A. (2022) · Infection and Immunity · doi:10.1128/iai.00206-22 · Cited by 62 · see citing works

Borrelia burgdorferi : Carbon Metabolism and the Tick-Mammal Enzootic Cycle

Corona, A., & Schwartz, I. S. (2015) · Microbiology Spectrum · doi:10.1128/microbiolspec.mbp-0011-2014 · Cited by 62 · see citing works

Overlapping Repressor Binding Sites Result in Additive Regulation ofEscherichia coliFadH by FadR and ArcA

Feng, Y., & Cronan, J. E. (2010) · Journal of Bacteriology · doi:10.1128/jb.00516-10 · Cited by 62 · see citing works

Sugar Allocation to Metabolic Pathways is Tightly Regulated and Affects the Virulence of Streptococcus mutans

Kawada‐Matsuo, M., Oogai, Y., & Komatsuzawa, H. (2016) · Genes · doi:10.3390/genes8010011 · Cited by 62 · see citing works

A Comparative Analysis: Molecular Mechanisms of Carbon Catabolite Repression in Bacteria

Sonnleitner, E. (2025) · Annual Review of Microbiology · doi:10.1146/annurev-micro-050624-031622 · Cited by 23 · see citing works

La répression catabolique ou comment les bactéries choisissent leurs sucres préférés

Galinier, A. (2018) · médecine/sciences · doi:10.1051/medsci/20183406012 · Cited by 17 · see citing works

Advances in mechanism of Escherichia coli carbon catabo-literepression

Ma, W.-Q., Zhang, Z., Liu, Y., & Wang, H. (2010) · Hereditas (Beijing) · doi:10.3724/sp.j.1005.2010.00571 · Cited by 3 · see citing works

The Regulation Mechanism of Three Pathways on Carborn Catabolite Repression in Pseudomonas

We, G. (2014) · Current Biotechnology

Carbon catabolite repression in bacteria

Stülke, J., & Hillen, W. (1999) · Current Opinion in Microbiology · doi:10.1016/s1369-5274(99)80034-4 · Cited by 468 · see citing works