Literature DB >> 15748982

The role of isocitrate lyase and the glyoxylate cycle in Escherichia coli growing under glucose limitation.

Ram Prasad Maharjan1, Pak-Lam Yu, Shona Seeto, Thomas Ferenci.   

Abstract

Escherichia coli changes its metabolism in response to environmental circumstances, and metabolic adaptations are evident in hungry bacteria growing slowly in glucose-limited chemostats. The role of isocitrate lyase (AceA) was examined in E. coli growing under glucose limitation. AceA activity was elevated in a strain-dependent manner in the commonly used E. coli K-12 laboratory strains MG1655 and MC4100, but an aceA disruption surprisingly increased fitness under glucose limitation in both strains. However, in bacteria adapted to limiting glucose in long-term chemostats, mutations outside aceA changed its role from a negative to a positive influence. These results suggest that a recently proposed pathway of central metabolism involving the glyoxylate cycle enzymes is redundant in wild-type bacteria, but may take on a beneficial role after context adaptation. Interestingly, the aceA gene sequence did not alter during prolonged selection, so mutations in unidentified genes changed the metabolic context of unaltered AceA from a negative to a positive influence in bacteria highly adapted to limiting glucose.

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Year:  2004        PMID: 15748982     DOI: 10.1016/j.resmic.2004.09.004

Source DB:  PubMed          Journal:  Res Microbiol        ISSN: 0923-2508            Impact factor:   3.992


  16 in total

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Authors:  Pablo I Nikel; Jiangfeng Zhu; Ka-Yiu San; Beatriz S Méndez; George N Bennett
Journal:  J Bacteriol       Date:  2009-06-26       Impact factor: 3.490

3.  Mycobacterium smegmatis MSMEG_3705 encodes a selective major facilitator superfamily efflux pump with multiple roles.

Authors:  Zhen Zhang; Rui Wang; Jianping Xie
Journal:  Curr Microbiol       Date:  2015-02-20       Impact factor: 2.188

4.  Acetate Exposure Determines the Diauxic Behavior of Escherichia coli during the Glucose-Acetate Transition.

Authors:  Brice Enjalbert; Muriel Cocaign-Bousquet; Jean-Charles Portais; Fabien Letisse
Journal:  J Bacteriol       Date:  2015-07-27       Impact factor: 3.490

5.  Nonlinear dependency of intracellular fluxes on growth rate in miniaturized continuous cultures of Escherichia coli.

Authors:  Annik Nanchen; Alexander Schicker; Uwe Sauer
Journal:  Appl Environ Microbiol       Date:  2006-02       Impact factor: 4.792

6.  Cyclic AMP-dependent catabolite repression is the dominant control mechanism of metabolic fluxes under glucose limitation in Escherichia coli.

Authors:  Annik Nanchen; Alexander Schicker; Olga Revelles; Uwe Sauer
Journal:  J Bacteriol       Date:  2008-01-25       Impact factor: 3.490

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Journal:  Indian J Microbiol       Date:  2011-08-13       Impact factor: 2.461

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Authors:  Hendrik Waegeman; Joeri Beauprez; Helena Moens; Jo Maertens; Marjan De Mey; Maria R Foulquié-Moreno; Joseph J Heijnen; Daniel Charlier; Wim Soetaert
Journal:  BMC Microbiol       Date:  2011-04-11       Impact factor: 3.605

9.  ¹³C metabolic flux analysis identifies an unusual route for pyruvate dissimilation in mycobacteria which requires isocitrate lyase and carbon dioxide fixation.

Authors:  Dany J V Beste; Bhushan Bonde; Nathaniel Hawkins; Jane L Ward; Michael H Beale; Stephan Noack; Katharina Nöh; Nicholas J Kruger; R George Ratcliffe; Johnjoe McFadden
Journal:  PLoS Pathog       Date:  2011-07-21       Impact factor: 6.823

10.  Simple phenotypic sweeps hide complex genetic changes in populations.

Authors:  Ram P Maharjan; Bin Liu; Lu Feng; Thomas Ferenci; Lei Wang
Journal:  Genome Biol Evol       Date:  2015-01-13       Impact factor: 3.416

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