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

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

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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

Metabolic Regulation and Engineering Strategies of Carbon and Nitrogen Metabolism in Escherichia coli

Zhang, J., Fang, H., Du, G., & Zhang, D. (2025) · ACS Synthetic Biology · doi:10.1021/acssynbio.5c00039 · Cited by 19

Enhanced Production of Polymyxin E in Paenibacillus polymyxa by Replacement of Glucose by Starch

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Effect of Fructooligosaccharide Metabolism on Chicken Colonization by an Extra-Intestinal Pathogenic Escherichia coli Strain

Porcheron, G., Chanteloup, N., Trotereau, A., Brée, A., & Schouler, C. (2012) · PLoS ONE · doi:10.1371/journal.pone.0035475 · Cited by 19

Reconstruction of Transcription Control Networks in Mollicutes by High-Throughput Identification of Promoters

Fisunov, G. Y., Garanina, I. A., Evsyutina, D. V., Semashko, T. A., Nikitina, A. S., & Govorun, V. M. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.01977 · Cited by 22

Engineering of Klebsiella oxytoca for production of 2,3-butanediol via simultaneous utilization of sugars from a Golenkinia sp. hydrolysate

Park, J. H., Choi, M. A., Kim, Y. J., Kim, Y., Chang, Y. K., & Jeong, K. J. (2017) · Bioresource Technology · doi:10.1016/j.biortech.2017.05.111 · Cited by 19

Growth Rate-Dependent Control in Enterococcus faecalis: Effects on the Transcriptome and Proteome, and Strong Regulation of Lactate Dehydrogenase

Mehmeti, I., Færgestad, E. M., Bekker, M., Snipen, L. G., Nes, I. F., & Holo, H. (2011) · Applied and Environmental Microbiology · doi:10.1128/aem.06604-11 · Cited by 19

Biochemistry and regulatory functions of bacterial glucose kinases

Romero-Rodríguez, A., Ruiz‐Villafán, B., Rocha-Mendoza, D., Manzo‐Ruiz, M., & Sánchez, S. (2015) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2015.05.001 · Cited by 19

Regulation of Gene Expression

Kumar, A., Garg, S., & Garg, N. (2014) · Encyclopedia of Molecular Cell Biology and Molecular Medicine · doi:10.1002/3527600906.mcb.200400080.pub3 · Cited by 19

Advances in microbial nitrogen metabolism: synergizing technological innovations to drive systems biology and sustainable biotechnology

Du, Y., Wu, X., Gao, L., & Yang, F. (2025) · Bioresource Technology · doi:10.1016/j.biortech.2025.133153 · Cited by 19

Rhamnolipids Induced by Glycerol Enhance Dibenzothiophene Biodegradation in Burkholderia sp. C3

Ramírez, C. A. O., Kwan, A., & Li, Q. X. (2020) · Engineering · doi:10.1016/j.eng.2020.01.006 · Cited by 18

Escherichia coli Uses a Dedicated Importer and Desulfidase To Ferment Cysteine

Zhou, Y., & Imlay, J. A. (2022) · mBio · doi:10.1128/mbio.02965-21 · Cited by 18

New xylose transporters support the simultaneous consumption of glucose and xylose in Escherichia coli

Zhu, X., Fan, F., Qiu, H., Shao, M., Li, D., Yu, Y. H., Bi, C., & Zhang, X. (2022) · mLife · doi:10.1002/mlf2.12021 · Cited by 19

A sweet new set of inducible and constitutive promoters in Haloferax volcanii

Rados, T., Andre, K., Cerletti, M., & Filho, A. W. B. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1204876 · Cited by 18

Production of a bioflocculant fromKlebsiellasp. OS-1 using brewery wastewater as a source

Ma, L., Liang, J., Wang, S., Yang, B., Chen, M., & Liu, Y. (2017) · Environmental Technology · doi:10.1080/09593330.2017.1377770 · Cited by 18

A system-wide network reconstruction of gene regulation and metabolism in Escherichia coli

Grimbs, A., Klosik, D. F., Bornholdt, S., & Hütt, M. ‐. (2019) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1006962 · Cited by 18

Bacillus subtilis YlxR, Which Is Involved in Glucose-Responsive Metabolic Changes, Regulates Expression of tsaD for Protein Quality Control of Pyruvate Dehydrogenase

Ogura, M., Sato, T., & Abe, K. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.00923 · Cited by 17

Impact of the Histidine-Containing Phosphocarrier Protein HPr on Carbon Metabolism and Virulence in Staphylococcus aureus

Pätzold, L., Brausch, A.-C., Bielefeld, E.-L., Zimmer, L., Somerville, G. A., Bischoff, M., & Gaupp, R. (2021) · Microorganisms · doi:10.3390/microorganisms9030466 · Cited by 18

Phosphoproteome Study of Escherichia coli Devoid of Ser/Thr Kinase YeaG During the Metabolic Shift From Glucose to Malate

Sultan, A., Jers, C., Ganief, T. A., Shi, L., Senissar, M., Køhler, J. B., Maček, B., & Mijakovic̀, I. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.657562 · Cited by 19

Omics Approaches for Designing Biofuel Producing Cocultures for Enhanced Microbial Conversion of Lignocellulosic Substrates

Levin, D. B., Verbeke, T. J., Munir, R. I., Islam, R., Ramachandran, U., Lal, S., Schellenberg, J. J., & Sparling, R. (2015) · Elsevier eBooks · doi:10.1016/b978-0-444-59592-8.00017-8 · Cited by 18

Reverse diauxie phenotype in Pseudomonas aeruginosa biofilm revealed by exometabolomics and label-free proteomics

Yung, Y. P., McGill, S. L., Chen, H., Park, H., Carlson, R. P., & Hanley, L. (2019) · npj Biofilms and Microbiomes · doi:10.1038/s41522-019-0104-7 · Cited by 20

Microbial Interactions on Coral Surfaces and Within the Coral Holobiont

Teplitski, M., Krediet, C. J., Meyer, J. L., & Ritchie, K. B. (2016) · Springer eBooks · doi:10.1007/978-3-319-31305-4_21 · Cited by 16

Transcriptional Modulation of Transport- and Metabolism-Associated Gene Clusters Leading to Utilization of Benzoate in Preference to Glucose in Pseudomonas putida CSV86

Choudhary, A., Modak, A., Apte, S. K., & Phale, P. S. (2017) · Applied and Environmental Microbiology · doi:10.1128/aem.01280-17 · Cited by 17

Metabolic engineering of glycosylated polyketide biosynthesis

Pandey, R. P., Parajuli, P., & Sohng, J. K. (2018) · Emerging Topics in Life Sciences · doi:10.1042/etls20180011 · Cited by 17

PRD-Containing Virulence Regulators (PCVRs) in Pathogenic Bacteria

Rom, J. S., Hart, M. T., & McIver, K. S. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.772874 · Cited by 17

The Crp regulator of Pseudomonas putida : evidence of an unusually high affinity for its physiological effector, cAMP

Arce‐Rodríguez, A., Durante‐Rodríguez, G., Platero, R., Krell, T., Calles, B., & de Lorenzo, V. (2011) · Environmental Microbiology · doi:10.1111/j.1462-2920.2011.02622.x · Cited by 17

Genetic Analysis of the Functions and Interactions of Components of the LevQRST Signal Transduction Complex of Streptococcus mutans

Zeng, L., Das, S., & Burne, R. A. (2011) · PLoS ONE · doi:10.1371/journal.pone.0017335 · Cited by 17

Identification of trans - and cis -Control Elements Involved in Regulation of the Carbon Monoxide Dehydrogenase Genes in Mycobacterium sp. Strain JC1 DSM 3803

Oh, J., Park, S., Shin, S.-J., Ko, I.-J., Han, S. J., Park, S. W., Song, T., & Kim, Y. M. (2010) · Journal of Bacteriology · doi:10.1128/jb.00286-10 · Cited by 17

Biologically synthesized crude calcium lactate as a substrate for propylene glycol production

Binczarski, M. J., Berłowska, J., Stanishevsky, A. V., & Witońska, I. (2016) · RSC Advances · doi:10.1039/c6ra20722g · Cited by 17

Characterization of the Sorbitol Utilization Cluster of the Probiotic Pediococcus parvulus 2.6: Genetic, Functional and Complementation Studies in Heterologous Hosts

Pérez-Ramos, A., Werning, M. L., Prieto, A., Russo, P., Spano, G., Mohedano, M. L., & López, P. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.02393 · Cited by 17

La répression catabolique ou comment les bactéries choisissent leurs sucres préférés

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

Methyl Ketones from Municipal Solid Waste Blends by One‐Pot Ionic‐Liquid Pretreatment, Saccharification, and Fermentation

Yan, J., Liang, L., He, Q., Li, C., Xu, F., Sun, J., Goh, E.-B., Konda, N. V. S. N. M., Beller, H. R., Simmons, B. A., et al. (2019) · ChemSusChem · doi:10.1002/cssc.201901084 · Cited by 17

An enhancement strategy for the biodegradation of high-concentration aliphatic nitriles: Utilizing the glucose-mediated carbon catabolite repression mechanism

Li, C., Chen, X., Wen, L., Cheng, Y., An, X., Li, T., Zang, H., Zhao, X., Li, D., & Hou, N. (2020) · Environmental Pollution · doi:10.1016/j.envpol.2020.114302 · Cited by 17

Promoting cytidine biosynthesis by modulating pyrimidine metabolism and carbon metabolic regulatory networks in Bacillus subtilis

Zhang, X., Liu, L., Niu, P., Ye, T., Ding, W., Wei, X., Xu, J., Fang, H., & Liu, H. (2025) · Microbial Cell Factories · doi:10.1186/s12934-025-02731-y · Cited by 16

Single‐cell characterization of metabolic switching in the sugar phosphotransferase system ofEscherichia coli

Westermayer, S. A., Fritz, G., Gutiérrez, J., Megerle, J. A., Weißl, M. P. S., Schnetz, K., Gerland, U., & Rädler, J. O. (2016) · Molecular Microbiology · doi:10.1111/mmi.13329 · Cited by 16

Stoichiometric modelling of assimilatory and dissimilatory biomass utilisation in a microbial community

Hunt, K. A., Jennings, R. D., Inskeep, W. P., & Carlson, R. P. (2016) · Environmental Microbiology · doi:10.1111/1462-2920.13444 · Cited by 16

Pathway Engineering for Phenethylamine Production in Escherichia coli

Xu, D., & Zhang, L. (2020) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.0c01706 · Cited by 16

Metabolic engineering of Paenibacillus polymyxa for effective production of 2,3-butanediol from poplar hydrolysate

Zhang, J., Zhao, J., Fu, Q., Liu, H., Li, M., Wang, Z., Gu, W., Zhu, X., Lin, R., Dai, L., et al. (2023) · Bioresource Technology · doi:10.1016/j.biortech.2023.130002 · Cited by 16

Genomic and metabolomic analysis of Latilactobacillus sakei DCF0720 for black soybean yogurt fermentation

Lee, D. H., Lee, W., Shin, D., Im, H. C., Jung, G., Lee, Y.-B., & Choi, J. (2024) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2024.110897 · Cited by 16

GlaR (YugA)—a novel RpiR‐family transcription activator of the Leloir pathway of galactose utilization in Lactococcus lactis IL 1403

Aleksandrzak‐Piekarczyk, T., Szatraj, K., & Kosiorek, K. (2018) · MicrobiologyOpen · doi:10.1002/mbo3.714 · Cited by 16

New bacteriocin-like substances produced by Streptomyces species with activity against pathogens

Hernández-Saldaña, O. F., Barboza-Corona, J. E., Bideshi, D. K., & Vázquez, L. E. C. (2020) · Folia Microbiologica · doi:10.1007/s12223-020-00770-z · Cited by 16

Enzyme-mediated nutrient release: glucose-precursor activation by β-galactosidase to induce bacterial growth

Karton-Lifshin, N., Vogel, U., Sella, E., Seeberger, P. H., Shabat, D., & Lepenies, B. (2013) · Organic & Biomolecular Chemistry · doi:10.1039/c3ob27385g · Cited by 16

Engineering transport systems for microbial production

Onyeabor, M., Martinez, R., Kurgan, G., & Wang, X. (2020) · Advances in applied microbiology · doi:10.1016/bs.aambs.2020.01.002 · Cited by 17

Limited by sensing - A minimal stochastic model of the lag-phase during diauxic growth

Chu, D. (2016) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2016.10.019 · Cited by 15

Directed evolution of Zymomonas mobilis sugar facilitator Glf to overcome glucose inhibition

Kurgan, G., Onyeabor, M., Holland, S. C., Taylor, E., Schneider, A., Kurgan, L., Billings, T., & Wang, X. (2021) · Journal of Industrial Microbiology & Biotechnology · doi:10.1093/jimb/kuab066 · Cited by 15

Removing carbon catabolite repression in Parageobacillus thermoglucosidasius DSM 2542

Liang, J., van Kranenburg, R., Bolhuis, A., & Leak, D. J. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.985465 · Cited by 15

Effect of Funneliformis mosseae and Thiobacillus thioparus on sulfur utilization in soybean sterilized soil under continuous cropping

Liu, R., Chang, D., Sun, Z., Wu, Y., Zhang, X., Lu, C., Mao, Y., Chen, J., & Cai, B. (2023) · Plant and Soil · doi:10.1007/s11104-023-06081-9 · Cited by 15

Carbon source control of the phosphorylation state of the Bacillus subtilis carbon-flux regulator Crh in vivo

Landmann, J. J., Werner, S., Hillen, W., Stülke, J., & Görke, B. (2011) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2011.02456.x · Cited by 15

The three-legged stool of understanding metabolism: integrating metabolomics with biochemical genetics and computational modeling

Downs, D. M., Bazurto, J. V., Gupta, A. K., Fonseca, L. L., & Voit, E. O. (2018) · AIMS Microbiology · doi:10.3934/microbiol.2018.2.289 · Cited by 15

Tripartite Regulation of the glpFKD Operon Involved in Glycerol Catabolism by GylR, Crp, and SigF in Mycobacterium smegmatis

Bong, H.-J., Ko, E.-M., Song, S.-Y., Ko, I.-J., & Oh, J. (2019) · Journal of Bacteriology · doi:10.1128/jb.00511-19 · Cited by 15

Glucose-Mediated Protein Arginine Phosphorylation/Dephosphorylation Regulates ylxR Encoding Nucleoid-Associated Protein and Cell Growth in Bacillus subtilis

Ogura, M. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.590828 · Cited by 15

The secondary messenger ppGpp interferes with cAMP-CRP regulon by promoting CRP acetylation in Escherichia coli

Ro, C., Cashel, M., & Fernández‐Coll, L. (2021) · PLoS ONE · doi:10.1371/journal.pone.0259067 · Cited by 15

Interactions Between Streptococcus gordonii and Fusobacterium nucleatum Altered Bacterial Transcriptional Profiling and Attenuated the Immune Responses of Macrophages

Liu, T., Yang, R., Zhou, J., Lu, X., Yuan, Z., Wei, X., & Guo, L. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.783323 · Cited by 16

Dual Substrate Specificity of an N -Acetylglucosamine Phosphotransferase System in Clostridium beijerinckii

Makishah, N. H. A., & Mitchell, W. J. (2013) · Applied and Environmental Microbiology · doi:10.1128/aem.01866-13 · Cited by 15

Transcription of Sialic Acid Catabolism Genes in Corynebacterium glutamicum Is Subject to Catabolite Repression and Control by the Transcriptional Repressor NanR

Uhde, A., Brühl, N., Goldbeck, O., Matano, C., Gurow, O., Rückert, C., Marin, K., Wendisch, V. F., Krämer, R., & Seibold, G. M. (2016) · Journal of Bacteriology · doi:10.1128/jb.00820-15 · Cited by 14

Route of Glucose Uptake in the Group a Streptococcus Impacts SLS-Mediated Hemolysis and Survival in Human Blood

Sundar, G. S., Islam, E., Braza, R. E. D., Silver, A. B., Breton, Y. S. L., & McIver, K. S. (2018) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2018.00071 · Cited by 15

Transcriptional regulation of fatty acid cis – trans isomerization in the solvent‐tolerant soil bacterium, Pseudomonas putida F1

Kondakova, T., & Cronan, J. E. (2019) · Environmental Microbiology · doi:10.1111/1462-2920.14546 · Cited by 15

Comparative analysis of the gene expression profile of probiotic Lactobacillus casei Zhang with and without fermented milk as a vehicle during transit in a simulated gastrointestinal tract

Wang, J., Zhong, Z., Zhang, W., Bao, Q., Wei, A., Meng, H., & Zhang, H. (2012) · Research in Microbiology · doi:10.1016/j.resmic.2012.04.002 · Cited by 15

Interaction with Enzyme IIBMpo(EIIBMpo) and Phosphorylation by Phosphorylated EIIBMpoExert Antagonistic Effects on the Transcriptional Activator ManR of Listeria monocytogenes

Zébré, A. C., Aké, F. M., Ventroux, M., Koffi-Nevry, R., Noirot‐Gros, M., Deutscher, J., & Milohanic, E. (2015) · Journal of Bacteriology · doi:10.1128/jb.02522-14 · Cited by 17

Unifying themes and distinct features of carbon and nitrogen assimilation by polysaccharide-degrading bacteria: a summary of four model systems

Gardner, J. G., & Schreier, H. J. (2021) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-021-11614-2 · Cited by 14

Effects of carbon and nitrogen sources on the induction and repression of chitinase enzyme from Beauveria bassiana isolates

Priyanka, D., & Kaur, G. (2010) · AFRICAN JOURNAL OF BIOTECHNOLOGY · doi:10.5897/ajb09.1161 · Cited by 14

Effects of Different Carbon Sources on Enzyme Production and Ultrastructure of Cellulosimicrobium cellulans

Dou, T., Chen, J., Hao, Y.-F., & Qi, X. (2019) · Current Microbiology · doi:10.1007/s00284-019-01633-8 · Cited by 14

Preferred Hexoses Influence Long-Term Memory in and Induction of Lactose Catabolism by Streptococcus mutans

Zeng, L., Chen, L., & Burne, R. A. (2018) · Applied and Environmental Microbiology · doi:10.1128/aem.00864-18 · Cited by 14

Phage-mediated transfer of a dextranase gene in Lactobacillus sanfranciscensis and characterization of the enzyme

Picozzi, C., Meißner, D., Chierici, M., Ehrmann, M. A., Vigentini, I., Foschino, R. C., & Vogel, R. F. (2015) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2015.02.018 · Cited by 14

Transport and Catabolism of Pentitols by Listeria monocytogenes

Kentache, T., Milohanic, E., Cao, T. N., Mokhtari, A., Aké, F. M., Pham, Q. M. M., Joyet, P., & Deutscher, J. (2016) · Microbial Physiology · doi:10.1159/000447774 · Cited by 14

Understanding LrgAB Regulation of Streptococcus mutans Metabolism

Ahn, S., Hull, W., Desai, S., Rice, K. C., & Culp, D. J. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.02119 · Cited by 14

Benzoate mediates the simultaneous repression of anaerobic 4-methylbenzoate and succinate utilization in Magnetospirillum sp. strain pMbN1

Lahme, S., Trautwein, K., Strijkstra, A., Dörries, M., Wöhlbrand, L., & Rabus, R. (2014) · BMC Microbiology · doi:10.1186/preaccept-6383322813809955 · Cited by 14

Cyclic AMP-receptor protein activates aerobactin receptor IutA expression in Vibrio vulnificus

Kim, C., Kim, S., & Shin, S. (2012) · The Journal of Microbiology · doi:10.1007/s12275-012-2056-y · Cited by 14

The Structure of Mlc Titration Factor A (MtfA/YeeI) Reveals a Prototypical Zinc Metallopeptidase Related to Anthrax Lethal Factor

Xu, Q., Göhler, A.-K., Kosfeld, A., Carlton, D. D., Chiu, H., Klock, H. E., Knuth, M. W., Miller, M. D., Elsliger, M., Deacon, A. M., et al. (2012) · Journal of Bacteriology · doi:10.1128/jb.00038-12 · Cited by 14

Investigation into the treatment and resource recovery of rifamycin mycelial dreg with thermal alkaline pretreatment-anaerobic digestion

Zhang, Q., Gong, X., Zhang, Y., Wang, X., Pan, X., Zhou, Y., Xu, X., Zhang, Q., Ji, X.-M., Wang, W., et al. (2023) · Journal of Cleaner Production · doi:10.1016/j.jclepro.2023.139169 · Cited by 13

Label‐free quantification reveals major proteomic changes in Pseudomonas putida F1 during the exponential growth phase

Herbst, F., Danielsen, H. N., Wimmer, R., Nielsen, P. H., & Dueholm, M. S. (2015) · PROTEOMICS · doi:10.1002/pmic.201400482 · Cited by 13

The phosphocarrier protein HPr of N eisseria meningitidis interacts with the transcription regulator CrgA and its deletion affects capsule production, cell adhesion, and virulence

Derkaoui, M., Antunes, A. P. D. O. L., Poncet, S., Abdallah, J. N., Joyet, P., Mazé, A., Henry, C., Taha, M., Deutscher, J., & Deghmane, A. (2016) · Molecular Microbiology · doi:10.1111/mmi.13349 · Cited by 13

The Bacillus cereus Group

Ramarao, N., Lereclus, D., & Sorokin, A. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-397169-2.00059-7 · Cited by 14

Multi-wavelength analytical ultracentrifugation as a tool to characterise protein–DNA interactions in solution

Horne, C. R., Henrickson, A., Demeler, B., & Dobson, R. C. J. (2020) · European Biophysics Journal · doi:10.1007/s00249-020-01481-6 · Cited by 13

Availability of the Molecular Switch XylR Controls Phenotypic Heterogeneity and Lag Duration during Escherichia coli Adaptation from Glucose to Xylose

Barthe, M., Tchouanti, J., Gomes, P., Bideaux, C., Lestrade, D., Graham, C., Steyer, J., Méléard, S., Harmand, J., Gorret, N., et al. (2020) · mBio · doi:10.1128/mbio.02938-20 · Cited by 15

Phenotypic differences between Edwardsiella piscicida and Edwardsiella anguillarum isolates in Japan

Sugiura, H., Fukunishi, K., Kawakami, H., & Imajoh, M. (2022) · Journal of Aquatic Animal Health · doi:10.1002/aah.10169 · Cited by 13

Optimization of gelatinolytic enzyme production by B. amyloliquefaciens sp. H11 through Plackett–Burman design and response surface methodology

Sai‐Ut, S., Benjakul, S., Sumpavapol, P., & Kishimura, H. (2014) · International aquatic research. · doi:10.1007/s40071-014-0059-5 · Cited by 13

Alkaline conditions stimulate the production of 1,3-propanediol in Lactobacillus panis PM1 through shifting metabolic pathways

Grahame, D. A. S., Kang, T. S., Khan, N. H., & Tanaka, T. (2013) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-013-1283-7 · Cited by 13

GxySBA ABC Transporter of Agrobacterium tumefaciens and Its Role in Sugar Utilization and vir Gene Expression

Zhao, J., & Binns, A. N. (2014) · Journal of Bacteriology · doi:10.1128/jb.01648-14 · Cited by 13

Probing the regulatory effects of specific mutations in three major binding domains of the pleiotropic regulator CcpA of Bacillus subtilis

Weme, R. D. O., Seidel, G., & Kuipers, O. P. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.01051 · Cited by 13

The impact of mixtures of xylose and glucose on the microbial diversity and fermentative metabolism of sequencing-batch or continuous enrichment cultures

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