Literature DB >> 18359269

The mechanisms of carbon catabolite repression in bacteria.

Josef Deutscher1.   

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.

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Year:  2008        PMID: 18359269     DOI: 10.1016/j.mib.2008.02.007

Source DB:  PubMed          Journal:  Curr Opin Microbiol        ISSN: 1369-5274            Impact factor:   7.934


  215 in total

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Journal:  J Ind Microbiol Biotechnol       Date:  2017-08-03       Impact factor: 3.346

2.  Two gene clusters coordinate galactose and lactose metabolism in Streptococcus gordonii.

Authors:  Lin Zeng; Nicole C Martino; Robert A Burne
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3.  Spatial and temporal organization of the E. coli PTS components.

Authors:  Livnat Lopian; Yair Elisha; Anat Nussbaum-Shochat; Orna Amster-Choder
Journal:  EMBO J       Date:  2010-10-05       Impact factor: 11.598

4.  Growth rate-dependent control in Enterococcus faecalis: effects on the transcriptome and proteome, and strong regulation of lactate dehydrogenase.

Authors:  Ibrahim Mehmeti; Ellen M Faergestad; Martijn Bekker; Lars Snipen; Ingolf F Nes; Helge Holo
Journal:  Appl Environ Microbiol       Date:  2011-10-28       Impact factor: 4.792

5.  The Crc global regulator inhibits the Pseudomonas putida pWW0 toluene/xylene assimilation pathway by repressing the translation of regulatory and structural genes.

Authors:  Renata Moreno; Pilar Fonseca; Fernando Rojo
Journal:  J Biol Chem       Date:  2010-06-07       Impact factor: 5.157

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

Authors:  Clementina Dellomonaco; James M Clomburg; Elliot N Miller; Ramon Gonzalez
Journal:  Nature       Date:  2011-08-10       Impact factor: 49.962

Review 7.  Pseudomonad reverse carbon catabolite repression, interspecies metabolite exchange, and consortial division of labor.

Authors:  Heejoon Park; S Lee McGill; Adrienne D Arnold; Ross P Carlson
Journal:  Cell Mol Life Sci       Date:  2019-11-25       Impact factor: 9.261

8.  Dual substrate specificity of an N-acetylglucosamine phosphotransferase system in Clostridium beijerinckii.

Authors:  Naief H Al Makishah; Wilfrid J Mitchell
Journal:  Appl Environ Microbiol       Date:  2013-08-30       Impact factor: 4.792

9.  Malate-mediated carbon catabolite repression in Bacillus subtilis involves the HPrK/CcpA pathway.

Authors:  Frederik M Meyer; Matthieu Jules; Felix M P Mehne; Dominique Le Coq; Jens J Landmann; Boris Görke; Stéphane Aymerich; Jörg Stülke
Journal:  J Bacteriol       Date:  2011-10-14       Impact factor: 3.490

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

Authors:  Lin Zeng; Lulu Chen; Robert A Burne
Journal:  Appl Environ Microbiol       Date:  2018-07-02       Impact factor: 4.792

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