Literature DB >> 35065916

Inducer exclusion, by itself, cannot account for the glucose-mediated lac repression of Escherichia coli.

Ritesh Kumar Aggarwal1, Atul Narang2.   

Abstract

The lac operon of Escherichia coli is repressed several 100-fold in the presence of glucose. This repression has been attributed to cAMP receptor protein-mediated inhibition of lac transcription and EIIAGlc-mediated inhibition of lactose transport (inducer exclusion). The growing evidence against the first mechanism has led to the postulate that the repression is driven by inducer exclusion. Although inducer exclusion reduces the permease activity only 2-fold in fully induced cells, it could be more potent in partially induced cells. Here, we show that even in partially induced cells, inducer exclusion reduces the permease activity no more than 6-fold. Moreover, the repression is so small because these experiments are performed in the presence of chloramphenicol. Indeed, when glucose is added to a culture growing on glycerol and TMG, but no chloramphenicol, lac expression is repressed 900-fold. This repression is primarily due to reversal of the positive feedback loop, i.e., the decline of the intracellular TMG level leads to a lower permease level, which reduces the intracellular TMG level even further. The repression in the absence of chloramphenicol is therefore primarily due to positive feedback, which does not exist during measurements of inducer exclusion.
Copyright © 2022 Biophysical Society. Published by Elsevier Inc. All rights reserved.

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Year:  2022        PMID: 35065916      PMCID: PMC8943701          DOI: 10.1016/j.bpj.2022.01.016

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  35 in total

1.  Cyclic AMP as an antagonist of catabolite repression in Escherichia coli.

Authors:  A Ullmann; J Monod
Journal:  FEBS Lett       Date:  1968-11       Impact factor: 4.124

2.  lac operon induction in Escherichia coli: Systematic comparison of IPTG and TMG induction and influence of the transacetylase LacA.

Authors:  Anja Marbach; Katja Bettenbrock
Journal:  J Biotechnol       Date:  2011-11-03       Impact factor: 3.307

3.  Mechanism responsible for glucose-lactose diauxie in Escherichia coli: challenge to the cAMP model.

Authors:  T Inada; K Kimata; H Aiba
Journal:  Genes Cells       Date:  1996-03       Impact factor: 1.891

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Authors:  A L KOCH
Journal:  Ann N Y Acad Sci       Date:  1963-01-21       Impact factor: 5.691

5.  Bacterial gene regulation in diauxic and non-diauxic growth.

Authors:  Atul Narang; Sergei S Pilyugin
Journal:  J Theor Biol       Date:  2006-08-12       Impact factor: 2.691

6.  Combinatorial transcriptional control of the lactose operon of Escherichia coli.

Authors:  Thomas Kuhlman; Zhongge Zhang; Milton H Saier; Terence Hwa
Journal:  Proc Natl Acad Sci U S A       Date:  2007-03-21       Impact factor: 11.205

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Authors:  B L Wanner; R Kodaira; F C Neidhardt
Journal:  J Bacteriol       Date:  1978-12       Impact factor: 3.490

Review 8.  Carbon catabolite repression in bacteria: many ways to make the most out of nutrients.

Authors:  Boris Görke; Jörg Stülke
Journal:  Nat Rev Microbiol       Date:  2008-08       Impact factor: 60.633

9.  Phosphoenolpyruvate:sugar phosphotransferase system-mediated regulation of carbohydrate metabolism in Salmonella typhimurium.

Authors:  S O Nelson; B J Scholte; P W Postma
Journal:  J Bacteriol       Date:  1982-05       Impact factor: 3.490

10.  Positive feedback exists and drives the glucose-mediated repression in Escherichia coli.

Authors:  Ritesh Kumar Aggarwal; Atul Narang
Journal:  Biophys J       Date:  2022-01-20       Impact factor: 4.033

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  1 in total

1.  Positive feedback exists and drives the glucose-mediated repression in Escherichia coli.

Authors:  Ritesh Kumar Aggarwal; Atul Narang
Journal:  Biophys J       Date:  2022-01-20       Impact factor: 4.033

  1 in total

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