Literature DB >> 1645125

A dominant mutation in the gene for the Nag repressor of Escherichia coli that renders the nag regulon uninducible.

J A Plumbridge1.   

Abstract

The gene nagC encodes the repressor for the nag regulon. A point mutation within the gene, which confers a super-repressor phenotype and makes the repressor insensitive to the inducer, N-acetylglucosamine 6-phosphate, has been characterized. The mutation is semi-dominant since heterozygous diploids have reduced growth rates on glucosamine and N-acetylglucosamine compared to the wild-type strain.

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Year:  1992        PMID: 1645125     DOI: 10.1099/00221287-138-5-1011

Source DB:  PubMed          Journal:  J Gen Microbiol        ISSN: 0022-1287


  10 in total

1.  GlcNAc-6P levels modulate the expression of Curli fibers by Escherichia coli.

Authors:  Michelle M Barnhart; Jaclyn Lynem; Matthew R Chapman
Journal:  J Bacteriol       Date:  2006-07       Impact factor: 3.490

Review 2.  Linkage map of Escherichia coli K-12, edition 10: the traditional map.

Authors:  M K Berlyn
Journal:  Microbiol Mol Biol Rev       Date:  1998-09       Impact factor: 11.056

3.  How to achieve constitutive expression of a gene within an inducible operon: the example of the nagC gene of Escherichia coli.

Authors:  J Plumbridge
Journal:  J Bacteriol       Date:  1996-05       Impact factor: 3.490

4.  Why does Escherichia coli grow more slowly on glucosamine than on N-acetylglucosamine? Effects of enzyme levels and allosteric activation of GlcN6P deaminase (NagB) on growth rates.

Authors:  Laura I Alvarez-Añorve; Mario L Calcagno; Jacqueline Plumbridge
Journal:  J Bacteriol       Date:  2005-05       Impact factor: 3.490

5.  Identification of a dedicated recycling pathway for anhydro-N-acetylmuramic acid and N-acetylglucosamine derived from Escherichia coli cell wall murein.

Authors:  J T Park
Journal:  J Bacteriol       Date:  2001-07       Impact factor: 3.490

6.  An alternative route for recycling of N-acetylglucosamine from peptidoglycan involves the N-acetylglucosamine phosphotransferase system in Escherichia coli.

Authors:  Jacqueline Plumbridge
Journal:  J Bacteriol       Date:  2009-07-17       Impact factor: 3.490

7.  Allosteric regulation of glucosamine-6-phosphate deaminase (NagB) and growth of Escherichia coli on glucosamine.

Authors:  Laura I Alvarez-Añorve; Ismael Bustos-Jaimes; Mario L Calcagno; Jacqueline Plumbridge
Journal:  J Bacteriol       Date:  2009-08-21       Impact factor: 3.490

8.  Physiological studies of Escherichia coli strain MG1655: growth defects and apparent cross-regulation of gene expression.

Authors:  Eric Soupene; Wally C van Heeswijk; Jacqueline Plumbridge; Valley Stewart; Daniel Bertenthal; Haidy Lee; Gyaneshwar Prasad; Oleg Paliy; Parinya Charernnoppakul; Sydney Kustu
Journal:  J Bacteriol       Date:  2003-09       Impact factor: 3.490

9.  Coordinated regulation of amino sugar-synthesizing and -degrading enzymes in Escherichia coli K-12.

Authors:  J A Plumbridge; O Cochet; J M Souza; M M Altamirano; M L Calcagno; B Badet
Journal:  J Bacteriol       Date:  1993-08       Impact factor: 3.490

10.  NagC represses N-acetyl-glucosamine utilization genes in Vibrio fischeri within the light organ of Euprymna scolopes.

Authors:  Yan Sun; Subhash C Verma; Haikel Bogale; Tim Miyashiro
Journal:  Front Microbiol       Date:  2015-07-17       Impact factor: 5.640

  10 in total

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