Literature DB >> 12535077

A new Escherichia coli metabolic competency: growth on fatty acids by a novel anaerobic beta-oxidation pathway.

John W Campbell1, Rachael M Morgan-Kiss, John E Cronan.   

Abstract

Escherichia coli uses fatty acids as a sole carbon and energy source during aerobic growth by means of the enzymes encoded by the fad regulon. We report that this bacterium can also grow on fatty acids under anaerobic conditions provided that a terminal respiratory electron acceptor such as nitrate is available. This anaerobic utilization pathway is distinct from the well-studied aerobic pathway in that (i). it proceeds normally in mutant strains lacking various enzymes of the aerobic pathway; (ii). it functions with fatty acids (octanoate and decanoate) that cannot be used by wild-type E. coli strains under aerobic conditions; and (iii). super-repressor mutants of the fadR regulatory locus that block aerobic growth on fatty acids fail to block the anaerobic pathway. We have identified homologues of the FadA, FadB and FadD proteins required for aerobic fatty acid utilization called YfcY, YfcX and YdiD, respectively, which are involved in anaerobic growth on fatty acids. A strong FadR binding site was detected upstream of the yfcY gene consistent with microarray analyses, indicating that yfcYX expression is negatively regulated by FadR under aerobic growth conditions. In contrast, transcriptional regulation of ydiD appears to be independent of FadR, and anaerobic growth on fatty acids is not under FadR control. These three genes are conserved in the available genome sequences of pathogenic E. coli, Shigella and Salmonella strains.

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Year:  2003        PMID: 12535077     DOI: 10.1046/j.1365-2958.2003.03341.x

Source DB:  PubMed          Journal:  Mol Microbiol        ISSN: 0950-382X            Impact factor:   3.501


  73 in total

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3.  Large-scale analysis of gene clustering in bacteria.

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4.  The fate of linoleic acid on Saccharomyces cerevisiae metabolism under aerobic and anaerobic conditions.

Authors:  Francesca Casu; Farhana R Pinu; Eliezer Stefanello; David R Greenwood; Silas G Villas-Bôas
Journal:  Metabolomics       Date:  2018-07-24       Impact factor: 4.290

5.  Assessment of heterologous butyrate and butanol pathway activity by measurement of intracellular pathway intermediates in recombinant Escherichia coli.

Authors:  Curt R Fischer; Hsien-Chung Tseng; Mitchell Tai; Kristala L J Prather; Gregory Stephanopoulos
Journal:  Appl Microbiol Biotechnol       Date:  2010-07-13       Impact factor: 4.813

6.  Overlapping repressor binding sites result in additive regulation of Escherichia coli FadH by FadR and ArcA.

Authors:  Youjun Feng; John E Cronan
Journal:  J Bacteriol       Date:  2010-07-09       Impact factor: 3.490

7.  Copper response regulator1-dependent and -independent responses of the Chlamydomonas reinhardtii transcriptome to dark anoxia.

Authors:  Anja Hemschemeier; David Casero; Bensheng Liu; Christoph Benning; Matteo Pellegrini; Thomas Happe; Sabeeha S Merchant
Journal:  Plant Cell       Date:  2013-09-06       Impact factor: 11.277

8.  Transcriptional Repression of the VC2105 Protein by Vibrio FadR Suggests that It Is a New Auxiliary Member of the fad Regulon.

Authors:  Rongsui Gao; Jingxia Lin; Han Zhang; Youjun Feng
Journal:  Appl Environ Microbiol       Date:  2016-04-18       Impact factor: 4.792

9.  Isolation of improved free fatty acid overproducing strains of Escherichia coli via Nile red based high-throughput screening.

Authors:  Spencer W Hoover; J Tyler Youngquist; Phil A Angart; Sydnor T Withers; Rebecca M Lennen; Brian F Pfleger
Journal:  Environ Prog Sustain Energy       Date:  2011-11-17       Impact factor: 2.431

10.  Multiple FadD acyl-CoA synthetases contribute to differential fatty acid degradation and virulence in Pseudomonas aeruginosa.

Authors:  Yun Kang; Jan Zarzycki-Siek; Chad B Walton; Michael H Norris; Tung T Hoang
Journal:  PLoS One       Date:  2010-10-21       Impact factor: 3.240

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