Literature DB >> 363696

Energy supply for active transport in anaerobically grown Escherichia coli.

J Boonstra, J A Downie, W N Konings.   

Abstract

Escherichia coli K-12, grown under anaerobic conditions with glucose as the sole source of carbon and energy without any terminal electron acceptor added, contains a fumarate reductase system in which electrons are transferred from formate or reduced nicotinamide adenine dinucleotide via menaquinone and cytochromes to fumarate reductase. This fumarate reductase system plays an important role in the metabolic energy supply of E. coli, grown under so-called "glycolytic conditions," as is indicated by the growth yields and maximal growth rates of mutants impaired in electron transfer or adenosine triphosphatase (uncB). In mutants deficient in menaquinone, cytochromes, or fumarate reductase, these values are considerably lower than in mutants deficient in ubiquinone or a functional adenosine triphosphatase. Electron transfer in this fumarate reductase system leads to the generation of a membrane potential, as is indicated by the uptake of the lipophilic cation triphenylmethylphosphonium by membrane vesicles prepared from cytochrome-sufficient and uncB cells. The generation of a proton-motive force by the fumarate reductase system was also demonstrated by the uptake of amino acids under anaerobic conditions in membrane vesicles of cytochrome containing and uncB cells grown under glycolytic conditions. Membrane vesicles of cytochrome-deficient cells failed to accumulate triphenyl-methylphosphonium and amino acids under these conditions, indicating that cytochromes are essential for the generation of a proton-motive force. Using glutamine uptake as an indication of the generation of ATP and proline uptake as an indication of the generation of a proton-motive force, it was demonstrated in whole cells that the proton-motive force is formed by ATP hydrolysis in cytochrome-deficient cells and by electron transfer in the uncB cells. In cytochrome-containing cells it was not possible to distinguish between these two possibilities, but the growth parameters suggest that, under glycolytic conditions, the proton-motive force is generated via electron transfer in the fumarate reductase system rather than via ATP hydrolysis.

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Year:  1978        PMID: 363696      PMCID: PMC218517          DOI: 10.1128/jb.136.3.844-853.1978

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  43 in total

1.  Anaerobic transport in Escherichia coli membrane vesicles.

Authors:  J Boonstra; M T Huttunen; W N Konings
Journal:  J Biol Chem       Date:  1975-09-10       Impact factor: 5.157

2.  The electrochemical proton gradient in Escherichia coli membrane vesicles.

Authors:  S Ramos; H R Kaback
Journal:  Biochemistry       Date:  1977-03-08       Impact factor: 3.162

3.  Molecular biology and energetics of membrane transport.

Authors:  H R Kaback
Journal:  J Cell Physiol       Date:  1976-12       Impact factor: 6.384

4.  The relationship between the electrochemical proton gradient and active transport in Escherichia coli membrane vesicles.

Authors:  S Ramos; H R Kaback
Journal:  Biochemistry       Date:  1977-03-08       Impact factor: 3.162

5.  The anaerobic oxidation of dihydroorotate by Escherichia coli K-12.

Authors:  S Andrews; G B Cox; F Gibson
Journal:  Biochim Biophys Acta       Date:  1977-10-12

6.  Protein measurement with the Folin phenol reagent.

Authors:  O H LOWRY; N J ROSEBROUGH; A L FARR; R J RANDALL
Journal:  J Biol Chem       Date:  1951-11       Impact factor: 5.157

7.  Sequence of b cytochromes relative to ubiquinone in the electron transport chain of Escherichia coli.

Authors:  J A Downie; G B Cox
Journal:  J Bacteriol       Date:  1978-02       Impact factor: 3.490

8.  Generation of an electrochemical proton gradient by nitrate respiration in membrane vesicles from anaerobically grown Escherichia coli.

Authors:  J Boonstra; W N Konings
Journal:  Eur J Biochem       Date:  1977-09

9.  pH-dependent changes in proton:substrate stoichiometries during active transport in Escherichia coli membrane vesicles.

Authors:  S Ramos; H R Kaback
Journal:  Biochemistry       Date:  1977-09-20       Impact factor: 3.162

10.  Mutants of Escherichia coli K12 unable to use fumarate as an anaerobic electron acceptor.

Authors:  P R Lambden; J R Guest
Journal:  J Gen Microbiol       Date:  1976-12
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  7 in total

1.  Proteins induced by anaerobiosis in Escherichia coli.

Authors:  M W Smith; F C Neidhardt
Journal:  J Bacteriol       Date:  1983-04       Impact factor: 3.490

Review 2.  The respiratory chains of Escherichia coli.

Authors:  W J Ingledew; R K Poole
Journal:  Microbiol Rev       Date:  1984-09

3.  Use of phi(glp-lac) in studies of respiratory regulation of the Escherichia coli anaerobic sn-glycerol-3-phosphate dehydrogenase genes (glpAB).

Authors:  D R Kuritzkes; X Y Zhang; E C Lin
Journal:  J Bacteriol       Date:  1984-02       Impact factor: 3.490

4.  Genetic and physical characterization of lambda transducing phages (lambda frdA) containing the fumarate reductase gene of Escherichia coli K12.

Authors:  S T Cole; J R Guest
Journal:  Mol Gen Genet       Date:  1980

5.  Stimulatory effect of low ATP pools on transport of purine nucleosides in cells of Escherichia coli.

Authors:  A Munch-Petersen; N J Pihl
Journal:  Proc Natl Acad Sci U S A       Date:  1980-05       Impact factor: 11.205

6.  Analysis of the Actinobacillus pleuropneumoniae ArcA regulon identifies fumarate reductase as a determinant of virulence.

Authors:  Falk F R Buettner; Ibrahim M Bendallah; Janine T Bosse; Karla Dreckmann; John H E Nash; Paul R Langford; Gerald-F Gerlach
Journal:  Infect Immun       Date:  2008-03-31       Impact factor: 3.441

7.  Using synthetic biology to distinguish and overcome regulatory and functional barriers related to nitrogen fixation.

Authors:  Xia Wang; Jian-Guo Yang; Li Chen; Ji-Long Wang; Qi Cheng; Ray Dixon; Yi-Ping Wang
Journal:  PLoS One       Date:  2013-07-25       Impact factor: 3.240

  7 in total

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