Literature DB >> 6219670

Mutants of Escherichia coli H+-ATPase defective in the delta subunit of F1 and the b subunit of F0.

T Noumi, H Kanazawa.   

Abstract

Complete nucleotide sequence of the genes for subunits of the H+ ATPase of E.coli has been determined and several hybrid plasmids carrying various portions of these genes have been constructed. Genetic complementation and recombination tests of about forty mutants of E.coli defective in the ATPase were performed using these plasmids for identifying the locations of the mutations. Two mutants defective in the delta subunit and a novel type of mutant defective in the b subunit of F0 were identified. The delta subunit mutants showed no proton conduction, suggesting that this subunit has an important role for the proton conduction. The ATPase of the b subunit mutant has a normal activity of proton channel portion, which phenotype is clearly different from that of mutants of the b subunit reported previously.

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Year:  1983        PMID: 6219670     DOI: 10.1016/s0006-291x(83)80128-4

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  8 in total

1.  Photosynthetic ATPases: purification, properties, subunit isolation and function.

Authors:  S Merchant; B R Selman
Journal:  Photosynth Res       Date:  1985-03       Impact factor: 3.573

2.  Complementation between uncF alleles affecting assembly of the F1F0-ATPase complex of Escherichia coli.

Authors:  D A Jans; L Hatch; A L Fimmel; F Gibson; G B Cox
Journal:  J Bacteriol       Date:  1985-04       Impact factor: 3.490

3.  An acidic or basic amino acid at position 26 of the b subunit of Escherichia coli F1F0-ATPase impairs membrane proton permeability: suppression of the uncF469 nonsense mutation.

Authors:  D A Jans; L Hatch; A L Fimmel; F Gibson; G B Cox
Journal:  J Bacteriol       Date:  1984-11       Impact factor: 3.490

Review 4.  Structure and function of proton-translocating adenosine triphosphatase (F0F1): biochemical and molecular biological approaches.

Authors:  M Futai; H Kanazawa
Journal:  Microbiol Rev       Date:  1983-09

5.  Use of lambda unc transducing bacteriophages in genetic and biochemical characterization of H+-ATPase mutants of Escherichia coli.

Authors:  M E Mosher; L K Peters; R H Fillingame
Journal:  J Bacteriol       Date:  1983-12       Impact factor: 3.490

6.  Overproduction of subunit a of the F0 component of proton-translocating ATPase inhibits growth of Escherichia coli cells.

Authors:  H Kanazawa; T Kiyasu; T Noumi; M Futai
Journal:  J Bacteriol       Date:  1984-04       Impact factor: 3.490

7.  Synthesis of a functional F0 sector of the Escherichia coli H+-ATPase does not require synthesis of the alpha or beta subunits of F1.

Authors:  R H Fillingame; B Porter; J Hermolin; L K White
Journal:  J Bacteriol       Date:  1986-01       Impact factor: 3.490

Review 8.  Recent developments on structural and functional aspects of the F1 sector of H+-linked ATPases.

Authors:  P V Vignais; M Satre
Journal:  Mol Cell Biochem       Date:  1984       Impact factor: 3.396

  8 in total

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