Cited by 676Bacterial Genetics and BiotechnologyMicrobial Metabolic Engineering and BioproductionBiochemical and Molecular Research

The DOI matches its Crossref record; 52 of the 52 references it cites were found in a registry or an index.

The mechanisms of carbon catabolite repression in bacteria

Deutscher, Josef·2008·Current Opinion in Microbiology

DOI 10.1016/j.mib.2008.02.007

Open this paper in CoChat — free account

Abstract

Carbon catabolite repression (CCR) is the paradigm of cellular regulation. CCR happens when bacteria are exposed to two or more carbon sources and one of them is preferentially utilised (frequently glucose). CCR is often mediated by several mechanisms, which can either affect the synthesis of catabolic enzymes via global or specific regulators or inhibit the uptake of a carbon source and thus the formation of the corresponding inducer. The major CCR mechanisms operative in Enterobacteriaceae and Firmicutes are quite different, but in both types of organisms components of the phosphoenolpyruvate:carbohydrate phosphotransferase system (PTS) and protein phosphorylation play a major role. PTS-independent CCR mechanisms are operative in several other bacteria.

Integrity signals

Registry

Crossref · 10.1016/j.mib.2008.02.007

Cites

52 of 52 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

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
Self-citation
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
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
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
Correlation between Growth Rates, EIIA Crr Phosphorylation, and Intracellular Cyclic AMP Levels in Escherichia coli 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
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
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
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
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
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

Flagged first, then by citations

Show all 52 references

Sorted by citations

Items 201–300 of 676

LacR Is a Repressor of lacABCD and LacT Is an Activator of lacTFEG , Constituting the lac Gene Cluster in Streptococcus pneumoniae
Afzal, M., Shafeeq, S., & Kuipers, O. P. (2014) · Applied and Environmental Microbiology · doi:10.1128/aem.01370-14 · Cited by 33
Metabolic engineering of Propionibacterium freudenreichii subsp. shermanii for xylose fermentation
Wei, P., Lin, M. S., Wang, Z., Fu, H., Yang, H. K., Jiang, W., & Yang, S. (2016) · Bioresource Technology · doi:10.1016/j.biortech.2016.07.056 · Cited by 33
Causal mutations from adaptive laboratory evolution are outlined by multiple scales of genome annotations and condition-specificity
Phaneuf, P. V., Yurkovich, J. T., Heckmann, D., Wu, M., Sandberg, T. E., King, Z. A., Tan, J., Palsson, B. Ø., & Feist, A. M. (2020) · BMC Genomics · doi:10.1186/s12864-020-06920-4 · Cited by 32
CcpA forms complexes with CodY and RpoA in Bacillus subtilis
Wünsche, A., Hammer, E., Bartholomae, M., Völker, U., Burkovski, A., Seidel, G., & Hillen, W. (2012) · FEBS Journal · doi:10.1111/j.1742-4658.2012.08604.x · Cited by 33
The Crystal Structures of Apo and cAMP-Bound GlxR from Corynebacterium glutamicum Reveal Structural and Dynamic Changes upon cAMP Binding in CRP/FNR Family Transcription Factors
Townsend, P. D., Jungwirth, B., Pojer, F., Bußmann, M., Money, V. A., Cole, S. T., Pühler, A., Tauch, A., Bott, M. H., Cann, M. J., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0113265 · Cited by 32
An RNA thermometer dictates production of a secreted bacterial toxin
Twittenhoff, C., Heroven, A. K., Mühlen, S., Dersch, P., & Narberhaus, F. (2020) · PLoS Pathogens · doi:10.1371/journal.ppat.1008184 · Cited by 32
Global transcriptomic response of Listeria monocytogenes exposed to Fingered Citron (Citrus medica L. var. sarcodactylis Swingle) essential oil
Guo, J., Hu, X., Gao, Z., Li, G., Fu, F., Shang, X., Liang, Z., & Shan, Y. (2021) · Food Research International · doi:10.1016/j.foodres.2021.110274 · Cited by 32
GAPDH, as a Virulence Factor
Seidler, N. W. (2012) · Advances in experimental medicine and biology · doi:10.1007/978-94-007-4716-6_5 · Cited by 32
l -(+)-Lactic acid production by co-fermentation of cellobiose and xylose without carbon catabolite repression using Enterococcus mundtii QU 25
Wang, Y., Abdel‐Rahman, M. A., Tashiro, Y., Xiao, Y., Zendo, T., Sakai, K., & Sonomoto, K. (2014) · RSC Advances · doi:10.1039/c4ra02764g · Cited by 32
Comparative Transcriptome Analysis of Bacillus subtilis Responding to Dissolved Oxygen in Adenosine Fermentation
Yu, W., Gao, S.-H., Yin, C.-Y., Zhou, Y. Q., & Ye, B. (2011) · PLoS ONE · doi:10.1371/journal.pone.0020092 · Cited by 33
Role of Catabolite Control Protein A in the Regulation of Intermedilysin Production byStreptococcus intermedius
Tomoyasu, T., Tabata, A., Hiroshima, R., Imaki, H., Masuda, S., Whiley, R. A., Aduse‐Opoku, J., Kikuchi, K., Hiramatsu, K., & Nagamune, H. (2010) · Infection and Immunity · doi:10.1128/iai.00113-10 · Cited by 32
A novel arabinose-inducible genetic operation system developed for Clostridium cellulolyticum
Zhang, J., Liu, Y., Cui, G., & Cui, Q. (2015) · Biotechnology for Biofuels · doi:10.1186/s13068-015-0214-2 · Cited by 36
Catabolic flexibility of mammalian-associated lactobacilli
Donnell, M. M. O., O’Toole, P. W., & Ross, R. P. (2013) · Microbial Cell Factories · doi:10.1186/1475-2859-12-48 · Cited by 31
Certain Tomato Root Exudates Induced by Pseudomonas stutzeri NRCB010 Enhance Its Rhizosphere Colonization Capability
Zhang, H., Zheng, D., Hu, C., Cheng, W., Lei, P., Xu, H., & Gao, N. (2023) · Metabolites · doi:10.3390/metabo13050664 · Cited by 31
Reduced trace gas oxidizers as a response to organic carbon availability linked to oligotrophs in desert fertile islands
Li, S., Yang, S., Wei, X., Jiao, S., Luo, W., Chen, W., & Wei, G. (2023) · The ISME Journal · doi:10.1038/s41396-023-01437-6 · Cited by 31
CcpA and CodY Coordinate Acetate Metabolism in Streptococcus mutans
Kim, J. N., & Burne, R. A. (2017) · Applied and Environmental Microbiology · doi:10.1128/aem.03274-16 · Cited by 31
Adaptive Evolution of Escherichia coli Inactivated in the Phosphotransferase System Operon Improves Co-utilization of Xylose and Glucose Under Anaerobic Conditions
Balderas‐Hernández, V. E., Hernández‐Montalvo, V., Bolívar, F. G., Gosset, G., & Martı́nez, A. (2010) · Applied Biochemistry and Biotechnology · doi:10.1007/s12010-010-9056-3 · Cited by 30
Identification of catabolite control protein A from Staphylococcus aureus as a target of silver ions
Liao, X., Yang, F., Wang, R., He, X., Li, H., Kao, R. Y. T., Xia, W. T., & Sun, H. (2017) · Chemical Science · doi:10.1039/c7sc02251d · Cited by 30
An acetylatable lysine controls CRP function in E. coli
Davis, R., Conesa, A. É., Gallego‐Jara, J., Puente, T. D. D., Filippova, E. V., Kuffel, G. R., Anderson, W. F., Gibson, B. W., Schilling, B., Cánovas, M., et al. (2017) · Molecular Microbiology · doi:10.1111/mmi.13874 · Cited by 30
Fermentation of ginkgo biloba kernel juice using Lactobacillus plantarum Y2 from the ginkgo peel: Fermentation characteristics and evolution of phenolic profiles, antioxidant activities in vitro, and volatile flavor compounds
Yang, J., Sun, Y., Chen, J., Cheng, Y., Zhang, H., Gao, T., Xu, F., Pan, S., Tao, Y., & Lu, J. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.1025080 · Cited by 30
Small RNAs Involved in Regulation of Nitrogen Metabolism
Prasse, D., & Schmitz, R. A. (2018) · Microbiology Spectrum · doi:10.1128/microbiolspec.rwr-0018-2018 · Cited by 30
The GTPase BipA expressed at low temperature in Escherichia coli assists ribosome assembly and has chaperone-like activity
Choi, E., & Hwang, J. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.002295 · Cited by 29
How Bacterial Pathogens Coordinate Appetite with Virulence
Pokorzynski, N. D., & Groisman, E. A. (2023) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00198-22 · Cited by 31
Highly efficient production of rhamnolipid in P. putida using a novel sacB-based system and mixed carbon source
Pang, A., Wang, Y., Zhang, T., Gao, F., Shen, J., Huang, L., Zhou, J., Zhang, B., Liu, Z., & Zheng, Y. (2023) · Bioresource Technology · doi:10.1016/j.biortech.2023.130220 · Cited by 29
CcpA Coordinates Growth/Damage Balance for Streptococcus pyogenes Pathogenesis
Paluscio, E., Watson, M. E., & Caparon, M. G. (2018) · Scientific Reports · doi:10.1038/s41598-018-32558-0 · Cited by 28
Improved 2,3-butanediol yield and productivity from lignocellulose biomass hydrolysate in metabolically engineered Enterobacter aerogenes
Kim, D. G., Yoo, S. W., Kim, M., Ko, J. K., Um, Y., & Oh, M. (2020) · Bioresource Technology · doi:10.1016/j.biortech.2020.123386 · Cited by 29
Sustainable production and biomedical application of polymalic acid from renewable biomass and food processing wastes
Zou, X., Li, S., Wang, P., Li, B., Feng, Y., & Yang, S. (2020) · Critical Reviews in Biotechnology · doi:10.1080/07388551.2020.1844632 · Cited by 29
Controls on Bacterial Cell Envelope Sulfhydryl Site Concentrations: The Effect of Glucose Concentration During Growth
Yu, Q., & Fein, J. B. (2017) · Environmental Science & Technology · doi:10.1021/acs.est.7b01047 · Cited by 28
Optimizing a Fed-Batch High-Density Fermentation Process for Medium Chain-Length Poly(3-Hydroxyalkanoates) in Escherichia coli
Scheel, R. A., Ho, T., Kageyama, Y., Masisak, J., McKenney, S., Lundgren, B. R., & Nomura, C. T. (2021) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2021.618259 · Cited by 31
CcpA represses the expression of the divergent cit operons of Enterococcus faecalis through multiple cresites
Suárez, C. A., Blancato, V. S., Poncet, S., Deutscher, J., & Magni, C. (2011) · BMC Microbiology · doi:10.1186/1471-2180-11-227 · Cited by 28
Self-citation
Modulation of transcription antitermination in the bgl operon of Escherichia coli by the PTS
Raveh, H., Lopian, L., Nussbaum‐Shochat, A., Wright, A., & Amster‐Choder, O. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0902559106 · Cited by 28
Distinct Regulatory Role of Carbon Catabolite Protein A (CcpA) in Oral Streptococcal spxB Expression
Redanz, S., Masilamani, R., Cullin, N., Giacaman, R. A., Merritt, J. L., & Kreth, J. (2018) · Journal of Bacteriology · doi:10.1128/jb.00619-17 · Cited by 27
Fermentative Conversion of Two-Step Pre-Treated Lignocellulosic Biomass to Hydrogen
Kucharska, K., Cieśliński, H., Rybarczyk, P., Słupek, E., Łukajtis, R., Wychodnik, K., & Kamiński, M. (2019) · Catalysts · doi:10.3390/catal9100858 · Cited by 28
Strict and direct transcriptional repression of the pobA gene by benzoate avoids 4‐hydroxybenzoate degradation in the pollutant degrader bacterium Cupriavidus necator JMP134
Donoso, R. A., Pérez-Pantoja, D. R., & González, B. (2011) · Environmental Microbiology · doi:10.1111/j.1462-2920.2011.02470.x · Cited by 28
Metabolic engineering approaches for scale-up of fermentative biohydrogen production–A review
Akaniro, I. R., Oladipo, A. A., & Onwujekwe, E. C. (2023) · International Journal of Hydrogen Energy · doi:10.1016/j.ijhydene.2023.04.328 · Cited by 27
Production of polyhydroxyalkanoates by engineered Halomonas bluephagenesis using starch as a carbon source
Liu, Y., Song, X., Yang, W., Wang, M., Lian, G., & Li, Z. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.129838 · Cited by 27
Comparison and improvement of algorithms for computing minimal cut sets
Jungreuthmayer, C., Nair, G., Klamt, S., & Zanghellini, J. (2013) · BMC Bioinformatics · doi:10.1186/1471-2105-14-318 · Cited by 27
Regulation of fructooligosaccharide metabolism in an extra‐intestinal pathogenic Escherichia coli strain
Porcheron, G., Kut, E., Canépa, S., Maurel, M. C., & Schouler, C. (2011) · Molecular Microbiology · doi:10.1111/j.1365-2958.2011.07725.x · Cited by 27
Molecular mechanisms controlling fructose‐specific memory and catabolite repression in lactose metabolism by Streptococcus mutans
Zeng, L., & Burne, R. A. (2020) · Molecular Microbiology · doi:10.1111/mmi.14597 · Cited by 27
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) · ASM Press eBooks · doi:10.1128/9781683670131.ch27 · Cited by 31
Reprogramming T7RNA Polymerase in Escherichia coli Nissle 1917 under Specific Lac Operon for Efficient p -Coumaric Acid Production
Effendi, S. S. W., & Ng, I. (2022) · ACS Synthetic Biology · doi:10.1021/acssynbio.2c00363 · Cited by 27
The CRISPR technology: A promising strategy for improving dark fermentative biohydrogen production using Clostridium spp.
Husaini, C. U. N., Roslan, R., Ramzi, A. B., Luthfi, A. A. I., Tan, J. P., Lim, S. S., Ding, G., Jahim, J. M., & Abdul, P. M. (2023) · International Journal of Hydrogen Energy · doi:10.1016/j.ijhydene.2023.03.162 · Cited by 29
Exploration of bifurcated electron transfer mechanism in Bacillus cereus for enhanced power generation in double-chambered microbial fuel cells
Sreelekshmy, B. R., Basheer, R., & Shibli, S. M. A. (2022) · Journal of environmental chemical engineering · doi:10.1016/j.jece.2022.107601 · Cited by 26
Pseudomonas putida growing at low temperature shows increased levels of CrcZ and CrcY sRNAs, leading to reduced Crc‐dependent catabolite repression
Fonseca, P., Moreno, R., & Rojo, F. (2012) · Environmental Microbiology · doi:10.1111/j.1462-2920.2012.02708.x · Cited by 26
Catabolite control protein a of Streptococcus suis type 2 contributes to sugar metabolism and virulence
Tang, Y., Wu, W., Zhang, X., Lu, Z., Chen, J., & Fang, W. (2012) · The Journal of Microbiology · doi:10.1007/s12275-012-2035-3 · Cited by 26
Regulation of cid and lrg expression by CcpA in Streptococcus mutans
Kim, H., Waters, A., Turner, M. E., Rice, K. C., & Ahn, S. (2018) · Microbiology · doi:10.1099/mic.0.000744 · Cited by 25
Acetate overflow metabolism regulates a major metabolic shift after glucose depletion in Escherichia coli
Shimada, T., Nakazawa, K., Tachikawa, T., Saito, N., Niwa, T., Taguchi, H., & Tanaka, K. (2021) · FEBS Letters · doi:10.1002/1873-3468.14151 · Cited by 25
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. (2019) · ASM Press eBooks · doi:10.1128/9781683670131.ch26 · Cited by 28
Fungal lysis by a soil bacterium fermenting cellulose
Tolonen, A. C., Cerisy, T., Sayyed, H. E., Boutard, M., Salanoubat, M., & Church, G. M. (2014) · Environmental Microbiology · doi:10.1111/1462-2920.12495 · Cited by 25
Glucose 6P Binds and Activates HlyIIR to Repress Bacillus cereus Haemolysin hlyII Gene Expression
Guillemet, E., Tran, S., Cadot, C., Rognan, D., Lereclus, D., & Ramarao, N. (2013) · PLoS ONE · doi:10.1371/journal.pone.0055085 · Cited by 25
Real-Time Monitoring of Chemical Changes in Three Kinds of Fermented Milk Products during Fermentation Using Quantitative Difference Nuclear Magnetic Resonance Spectroscopy
Lü, Y., Ishikawa, H., Kwon, Y., Hu, F., Miyakawa, T., & Tanokura, M. (2018) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.7b05279 · Cited by 26
Diauxic growth of Clostridium acetobutylicum ATCC 824 when grown on mixtures of glucose and cellobiose
Buendia-Kandia, F., Rondags, E., Framboisier, X., Mauviel, G., Dufour, A., & Guédon, E. (2018) · AMB Express · doi:10.1186/s13568-018-0615-2 · Cited by 25
Newly Identified Nucleoid-Associated-Like Protein YlxR Regulates Metabolic Gene Expression in Bacillus subtilis
Ogura, M., & Kanesaki, Y. (2018) · mSphere · doi:10.1128/msphere.00501-18 · Cited by 25
Health improvement of human hair and their reshaping using recombinant keratin K31
Basit, A., Asghar, F., Sadaf, S., & Akhtar, M. (2018) · Biotechnology Reports · doi:10.1016/j.btre.2018.e00288 · Cited by 25
Regulation of microbial gene expression: the key to understanding our gut microbiome
Sinha, A. K., Laursen, M. F., & Licht, T. R. (2024) · Trends in Microbiology · doi:10.1016/j.tim.2024.07.005 · Cited by 27
Design of the lac gene circuit revisited
Savageau, M. A. (2011) · Mathematical Biosciences · doi:10.1016/j.mbs.2011.03.008 · Cited by 24
Changes of DNA topology affect the global transcription landscape and allow rapid growth of a Bacillus subtilis mutant lacking carbon catabolite repression
Reuß, D. R., Rath, H., Thürmer, A., Benda, M., Daniel, R., Völker, U., Mäder, U., Commichau, F. M., & Stülke, J. (2017) · Metabolic Engineering · doi:10.1016/j.ymben.2017.12.004 · Cited by 21
Type and capacity of glucose transport influences succinate yield in two-stage cultivations
Kyselova, L., Kreitmayer, D., Kremling, A., & Bettenbrock, K. (2018) · Microbial Cell Factories · doi:10.1186/s12934-018-0980-1 · Cited by 24
Enhancement of ascomycin production via a combination of atmospheric and room temperature plasma mutagenesis in Streptomyces hygroscopicus and medium optimization
Yu, Z., Shen, X., Wu, Y., Yang, S., Ju, D., & Chen, S. (2019) · AMB Express · doi:10.1186/s13568-019-0749-x · Cited by 24
Investigations on the influence of energy source on time-dependent hormesis: A case study of sulfadoxine to Aliivibrio fischeri in different cultivation systems
Gao, Q., Wang, J., Ren, L., Cheng, Y., Lin, Z., Li, X., & Sun, H. (2021) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2021.145877 · Cited by 24
Insight into Bacterial Phosphotransferase System-Mediated Signaling by Interspecies Transplantation of a Transcriptional Regulator
Bahr, T., Lüttmann, D., März, W., Rak, B., & Görke, B. (2011) · Journal of Bacteriology · doi:10.1128/jb.01459-10 · Cited by 24
Functional Roles of arcA , etrA , Cyclic AMP (cAMP)-cAMP Receptor Protein, and cya in the Arsenate Respiration Pathway in Shewanella sp. Strain ANA-3
Murphy, J. N., Durbin, K. J., & Saltikov, C. W. (2008) · Journal of Bacteriology · doi:10.1128/jb.01293-08 · Cited by 24
Efficient poly(3-hydroxybutyrate-co-lactate) production from corn stover hydrolysate by metabolically engineered Escherichia coli
Wu, J. Y., Wei, X., Guo, P., He, A., Xu, J., Jin, M., Zhang, Y., & Wu, H. C. (2021) · Bioresource Technology · doi:10.1016/j.biortech.2021.125873 · Cited by 23
AhrC Negatively Regulates Streptococcus mutans Arginine Biosynthesis
Jing, M., Zheng, T., Gong, T., Yan, J., Chen, J., Lin, Y., Tang, B., Ma, Q., Zhou, X., & Li, Y. (2022) · Microbiology Spectrum · doi:10.1128/spectrum.00721-22 · Cited by 22
Third-generation D-lactic acid production using red macroalgae Gelidium amansii by co-fermentation of galactose, glucose and xylose
Qiu, Z., Wang, G., Shao, W., Cao, L., Tan, H., Shao, S., Jin, C., Xia, J., He, J., Liu, X., et al. (2024) · Bioresource Technology · doi:10.1016/j.biortech.2024.130631 · Cited by 23
Thermoanaerobacterthermohydrosulfuricus WC1 Shows Protein Complement Stability during Fermentation of Key Lignocellulose-Derived Substrates
Verbeke, T. J., Spicer, V., Krokhin, O. V., Zhang, X., Schellenberg, J. J., Fristensky, B. W., Wilkins, J. A., Levin, D. B., & Sparling, R. (2013) · Applied and Environmental Microbiology · doi:10.1128/aem.03555-13 · Cited by 23
Optimization of β-galactosidase Production by Batch Cultures of Lactobacillus leichmannii 313 (ATCC 7830™)
Deng, Y., Xu, M., Ji, D., & Agyei, D. (2020) · Fermentation · doi:10.3390/fermentation6010027 · Cited by 23
Updates on Metabolism in Lactic Acid Bacteria in Light of “Omic” Technologies
Kowalczyk, M., Mayo, B., Fernández, M., & Aleksandrzak‐Piekarczyk, T. (2015) · Wiley eBooks · doi:10.1002/9781118868386.ch1 · Cited by 25
Identification and expression analysis of a gene encoding a shikimate transporter of Corynebacterium glutamicum
Kubota, T., Tanaka, Y., Takemoto, N., Hiraga, K., Yukawa, H., & Inui, M. (2014) · Microbiology · doi:10.1099/mic.0.083733-0 · Cited by 22
A non-linear model of hydrogen production by Caldicellulosiruptor saccharolyticus for diauxic-like consumption of lignocellulosic sugar mixtures
Björkmalm, J., Byrne, E., van Niel, E. W. J., & Willquist, K. (2018) · Biotechnology for Biofuels · doi:10.1186/s13068-018-1171-3 · Cited by 22
High efficiency biosynthesis of O-polysaccharide-based vaccines against extraintestinal pathogenic Escherichia coli
Jiang, X., Bai, J., Yuan, J., Zhang, H., Lu, G., Wang, Y., Jiang, L., Liu, B., Wang, L., Huang, D., et al. (2020) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2020.117475 · Cited by 22
Molecular mechanisms regulating the catabolic and electrochemical activities of Shewanella oneidensis MR-1
Kouzuma, A. (2021) · Bioscience Biotechnology and Biochemistry · doi:10.1093/bbb/zbab088 · Cited by 21
Deciphering the transcriptional regulation of the catabolism of lignin-derived aromatics in Rhodococcus opacus PD630
Diao, J.-J., Carr, R., & Moon, T. (2022) · Communications Biology · doi:10.1038/s42003-022-04069-2 · Cited by 18
Regulation of hierarchical carbon substrate utilization, nitrogen fixation, and root colonization by the Hfq/Crc/CrcZY genes in Pseudomonas stutzeri
Lv, F., Zhan, Y., Lü, W., Ke, X., Shao, Y., Ma, Y., Zheng, J., Yang, Z., Jiang, S., Shang, L., et al. (2022) · iScience · doi:10.1016/j.isci.2022.105663 · Cited by 22
Functional and structural diversification of incomplete phosphotransferase system in cellulose-degrading clostridia
Xu, T., Tao, X., He, H., Kempher, M. L., Zhang, S., Liu, X., Wang, J., Wang, D., Ning, D., Pan, C., et al. (2023) · The ISME Journal · doi:10.1038/s41396-023-01392-2 · Cited by 22
The Lcn972 Bacteriocin-Encoding Plasmid pBL1 Impairs Cellobiose Metabolism in Lactococcus lactis
Campelo, A. B., Gaspar, P., Roces, C., Rodrı́guez, A., Kok, J., Kuipers, O. P., Neves, A. R., & Martı́nez, B. (2011) · Applied and Environmental Microbiology · doi:10.1128/aem.06107-11 · Cited by 22
Catabolite regulation of enzymatic activities in a white pox pathogen and commensal bacteria during growth on mucus polymers from the coral Acropora palmata
Krediet, C. J., Ritchie, K., & Teplitski, M. (2009) · Diseases of Aquatic Organisms · doi:10.3354/dao02084 · Cited by 22
Streptococcus pyogenes Malate Degradation Pathway Links pH Regulation and Virulence
Paluscio, E., & Caparon, M. G. (2015) · Infection and Immunity · doi:10.1128/iai.02814-14 · Cited by 22
Contributions of SpoT Hydrolase, SpoT Synthetase, and RelA Synthetase to Carbon Source Diauxic Growth Transitions in Escherichia coli
Fernández‐Coll, L., & Cashel, M. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.01802 · Cited by 22
Carbohydrate-controlled serine protease inhibitor (serpin) production in Bifidobacterium longum subsp. longum
Duboux, S., Golliard, M., Muller, J. A., Bergonzelli, G. E., Bolten, C. J., Mercenier, A., & Kleerebezem, M. (2021) · Scientific Reports · doi:10.1038/s41598-021-86740-y · Cited by 23
The mRNA derived MalH sRNA contributes to alternative carbon source utilization by tuning maltoporin expression in E. coli
Iosub, I. A., Marchioretto, M., van Nues, R. W., McKellar, S. W., Viero, G., & Granneman, S. (2020) · RNA Biology · doi:10.1080/15476286.2020.1827784 · Cited by 21
Engineered l -Lactate Responding Promoter System Operating in Glucose-Rich and Anoxic Environments
Zúñiga, A., Rufino, M. C., Chang, H., Fristot, E., Mayonove, P., Hani, E.-H., & Bonnet, J. (2021) · ACS Synthetic Biology · doi:10.1021/acssynbio.1c00456 · Cited by 22
Avilamycin production enhancement by mutagenesis and fermentation optimization in Streptomyces viridochromogenes
Yu, G., Peng, H., Cao, J. J., Liao, A., Long, P., Huang, J., & Hui, M. (2022) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-021-03191-3 · Cited by 21
Carbon catabolite repression by seryl phosphorylated HPr is essential to S treptococcus pneumoniae in carbohydrate‐rich environments
FLEMING, E. M., Lazinski, D. W., & Camilli, A. (2015) · Molecular Microbiology · doi:10.1111/mmi.13033 · Cited by 21
Three dimensional optimisation for the enhancement of astaxanthin recovery from shrimp shell wastes by Aeromonas hydrophila
Cheong, J. Y., Muskhazli, M., Azwady, A. A. N., Ahmad, S. A., & Adli, A. A. (2020) · Biocatalysis and Agricultural Biotechnology · doi:10.1016/j.bcab.2020.101649 · Cited by 22
Genome‐wide analysis of in vivo CcpA binding with and without its key co‐factor HPr in the major human pathogen group A Streptococcus
DebRoy, S., Aliaga-Tobar, V., Galvez, G., Arora, S., Liang, X., Horstmann, N., Maracaja‐Coutinho, V., Latorre, M., Höök, M., Flores, A. R., et al. (2020) · Molecular Microbiology · doi:10.1111/mmi.14667 · Cited by 20
Lactic acid production using cheese whey based medium in a stirred tank reactor by a ccpA mutant of Lacticaseibacillus casei
Catone, M. V., Palomino, M. M., Legisa, D., Martin, J. F., Monedero, V., Ruzal, S. M., & Allievi, M. C. (2021) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-021-03028-z · Cited by 21
Fine-Tuned Transcriptional Regulation of Malate Operons in Enterococcus faecalis
Mortera, P., Espariz, M., Suárez, C. A., Repizo, G. D., Deutscher, J., Alarcón, S. H., Blancato, V. S., & Magni, C. (2012) · Applied and Environmental Microbiology · doi:10.1128/aem.07280-11 · Cited by 21
Self-citation
β-Glucoside metabolism in Oenococcus oeni: Cloning and characterisation of the phospho-β-glucosidase bglD
Capaldo, A., Walker, M. E., Ford, C. M., & Jiranek, V. (2010) · Food Chemistry · doi:10.1016/j.foodchem.2010.09.036 · Cited by 21
NagR Differentially Regulates the Expression of the glmS and nagAB Genes Required for Amino Sugar Metabolism by Streptococcus mutans
Zeng, L., & Burne, R. A. (2015) · Journal of Bacteriology · doi:10.1128/jb.00606-15 · Cited by 20
A galactose‐specific sugar: phosphotransferase permease is prevalent in the non‐core genome of S treptococcus mutans
Zeng, L., Xue, P., Stanhope, M. J., & Burne, R. A. (2013) · Molecular Oral Microbiology · doi:10.1111/omi.12025 · Cited by 20
Escherichia coli expressing endoglucanase gene from Thai higher termite bacteria for enzymatic and microbial hydrolysis of cellulosic materials
Seneesrisakul, K., Guralp, S. A., Gülari, E., & Chavadej, S. (2017) · Electronic Journal of Biotechnology · doi:10.1016/j.ejbt.2017.03.009 · Cited by 20
Unravelling the complexity and redundancy of carbon catabolic repression in Pseudomonas fluorescens SBW25
Liu, Y., Gokhale, C. S., Rainey, P. B., & Zhang, X. (2017) · Molecular Microbiology · doi:10.1111/mmi.13720 · Cited by 20
Enzymatic production of clickable and PEGylated recombinant polyhydroxyalkanoates
Vastano, M., Pellis, A., Immirzi, B., Poggetto, G. D., Malinconico, M., Sannia, G., Guebitz, G. M., & Pezzella, C. (2017) · Green Chemistry · doi:10.1039/c7gc01872j · Cited by 20
Deciphering global gene expression and regulation strategy in Escherichia coli during carbon limitation
Li, Z., Pan, Q., Xiao, Y., Fang, X., Shi, R., Fu, C., Danchin, A., & You, C. (2018) · Microbial Biotechnology · doi:10.1111/1751-7915.13343 · Cited by 18
Insights into the role of energy source in hormesis through diauxic growth of bacteria in mixed cultivation systems
Sun, H., Zhang, X., Wang, D., & Lin, Z. (2020) · Chemosphere · doi:10.1016/j.chemosphere.2020.127669 · Cited by 20
The maltose transporter subunit IICB of the phosphotransferase system: An important factor for biofilm formation of Cronobacter
Kong, X., Li, C., Sun, X., Niu, B., Guo, D., Jiang, Y., Yang, L., & Chen, Q. (2021) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2021.109517 · Cited by 20
Nitrogen starvation-induced transcriptome alterations and influence of transcription regulator mutants in Mycobacterium smegmatis
Jeßberger, N., Lü, Y., Amon, J., Titgemeyer, F., Sonnewald, S., Reid, S., & Burkovski, A. (2013) · BMC Research Notes · doi:10.1186/1756-0500-6-482 · Cited by 20
Carbon catabolite repression correlates with the maintenance of near invariant molecular crowding in proliferating E. coli cells
Zhou, Y., Vázquez, A., Wise, A. S., Warita, T., Warita, K., Bar‐Joseph, Z., & Oltvai, Z. N. (2013) · BMC Systems Biology · doi:10.1186/1752-0509-7-138 · Cited by 20
LMOf2365_0442 Encoding for a Fructose Specific PTS Permease IIA May Be Required for Virulence in L. monocytogenes Strain F2365
Liu, Y., Yoo, B. K., Hwang, C., Suo, Y., Sheen, S., Khosravi, P., & Huang, L. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.01611 · Cited by 20

Authors: Deutscher, J.
Affiliations: Centre National de la Recherche Scientifique (FR)
Corresponding author: Deutscher, Josef
ORCID: Deutscher, Josef
Venue: Current Opinion in Microbiology
Publisher: Elsevier BV
Published: 2008-04
Volume: 11
Issue: 2
Pages: 87-93
ISSN: 1369-5274 (ISSN-L)
DOI: 10.1016/j.mib.2008.02.007
OpenAlex: W2038683612
Cited by: 676
References: 52
Citations by year: 2026: 30 · 2025: 32 · 2024: 28 · 2023: 32 · 2022: 37 · 2021: 48 · 2020: 45 · 2019: 38 · 2018: 47 · 2017: 46 · 2016: 28 · 2015: 40 · 2014: 33 · 2013: 43 · 2012: 48
FWCI: 3.16
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Current Opinion in Microbiology (publishedVersion)
PubMed (publishedVersion)
HAL (submittedVersion)
Funders: Fonds De La Recherche Scientifique - FNRS
Topics: Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Microbial Metabolic Engineering and Bioproduction
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Biochemical and Molecular Research
Keywords: catabolite repression, glucose repression, phosphoenolpyruvate:carbohydrate phosphotransferase system, protein phosphorylation, Enterobacteriaceae, Firmicutes
MeSH terms: Bacteria, Bacterial Proteins, Carbon, Enterobacteriaceae, Phosphoenolpyruvate Sugar Phosphotransferase System, Transcription, Genetic, Signal Transduction, Gene Expression Regulation, Bacterial

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

The mechanisms of carbon catabolite repression in bacteria

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks