Literature DB >> 6460910

The genes for the eight subunits of the membrane bound ATP synthase of Escherichia coli.

F G Hansen, J Nielsen, E Riise, K von Meyenburg.   

Abstract

The genes for the eight subunits of the membrane bound ATP synthase of Escherichia coli (Ca++, Mg++ dependent ATPase, EC 3.6.1.3) were mapped through genetic, physical and functional analysis of specialized transducing phages lambda asn (von Meyenburg et al. 1978). The ATP synthase genes, designated atp1, are located at 83.2 min in a segment of the chromosome between 3.5 and 11.3 kb left (counterclockwise) of the origin of replication oriC. The counterclockwise order of the genes for the eight subunits, the expression of which starts from a control region at 3.5 kb-L, was found to be: a, (c, b, delta), alpha, gamma, (epsilon, beta) which in the notation of Downie el al. (1981) reads atp B (EFH) A G (C D). The analysis was in part based on the isolation of new types of atp (unc, Suc-) mutations. We made use of the fact that specialized transducing phages lambda asn carrying oriC can establish themselves as minichromosomes rendering asnA cells Asn+, and that the resulting Asn+ cells grow slowly if the lambda asn carries part or all of the atp operon. Selecting for fast growing strains mutations were isolated on the lambda asn which either eliminated atp genes or affected their expression ("promoter" mutations). The relationship between these atp mutations and the cop mutations of Ogura et al. (1980), which also appear to map in front of or within the atp genes, is discussed.

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Year:  1981        PMID: 6460910     DOI: 10.1007/bf00268766

Source DB:  PubMed          Journal:  Mol Gen Genet        ISSN: 0026-8925


  27 in total

1.  Characterization of the dnaA, gyrB and other genes in the dnaA region of the Escherichia coli chromosome on specialized transducing phages lambda tna.

Authors:  F G Hansen; K von Meyenburg
Journal:  Mol Gen Genet       Date:  1979-09

2.  A mutation affecting a second component of the F0 portion of the magnesium ion-stimulated adenosine triphosphatase of Escherichia coli K12. The uncC424 allele.

Authors:  F Gibson; G B Cox; J A Downie; J Radik
Journal:  Biochem J       Date:  1977-04-15       Impact factor: 3.857

3.  Plasmids carrying oriC can integrate at or near the chromosome origin of Escherichia coli in the absence of a functional recA product.

Authors:  M Masters; V Andresdottir; H Wolf-Watz
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1979

4.  The asparagine synthetase of Escherhic coli. I. Biosynthetic role of the enzyme, purification, and characterization of the reaction products.

Authors:  H Cedar; J H Schwartz
Journal:  J Biol Chem       Date:  1969-08-10       Impact factor: 5.157

5.  The isolated F0 of Escherichia coli aTP-synthase is reconstitutively active in H+-conduction and ATP-dependent energy-transduction.

Authors:  P Friedl; H U Schairer
Journal:  FEBS Lett       Date:  1981-06-15       Impact factor: 4.124

Review 6.  Linkage map of Escherichia coli K-12, edition 6.

Authors:  B J Bachmann; K B Low
Journal:  Microbiol Rev       Date:  1980-03

7.  The ATP synthetase of Escherichia coli K12: purification of the enzyme and reconstitution of energy-transducing activities.

Authors:  P Friedl; C Friedl; H U Schairer
Journal:  Eur J Biochem       Date:  1979-10

8.  Solubilization of the cytoplasmic membrane of Escherichia coli by the ionic detergent sodium-lauryl sarcosinate.

Authors:  C Filip; G Fletcher; J L Wulff; C F Earhart
Journal:  J Bacteriol       Date:  1973-09       Impact factor: 3.490

9.  Purification and properties of Mg2+-Ca2+ adenosinetriphosphatase from Escherichia coli.

Authors:  N Nelson; B I Kanner; D L Gutnick
Journal:  Proc Natl Acad Sci U S A       Date:  1974-07       Impact factor: 11.205

10.  Organization of unc gene cluster of Escherichia coli coding for proton-translocating ATPase of oxidative phosphorylation.

Authors:  H Kanazawa; F Tamura; K Mabuchi; T Miki; M Futai
Journal:  Proc Natl Acad Sci U S A       Date:  1980-12       Impact factor: 11.205

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  21 in total

Review 1.  Expression of the unc genes in Escherichia coli.

Authors:  J E McCarthy
Journal:  J Bioenerg Biomembr       Date:  1988-02       Impact factor: 2.945

Review 2.  The proton-ATPase of bacteria and mitochondria.

Authors:  A E Senior; J G Wise
Journal:  J Membr Biol       Date:  1983       Impact factor: 1.843

3.  Promoters of the atp operon coding for the membrane-bound ATP synthase of Escherichia coli mapped by Tn10 insertion mutations.

Authors:  K von Meyenburg; B B Jørgensen; J Nielsen; F G Hansen
Journal:  Mol Gen Genet       Date:  1982

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.  Cloning and expression of uncI, the first gene of the unc operon of Escherichia coli.

Authors:  W S Brusilow; A C Porter; R D Simoni
Journal:  J Bacteriol       Date:  1983-09       Impact factor: 3.490

6.  In vitro membrane association of the F0 polypeptides of the Escherichia coli proton translocating ATPase.

Authors:  K P Decker; W S Brusilow; R P Gunsalus; R D Simoni
Journal:  J Bacteriol       Date:  1982-11       Impact factor: 3.490

7.  Differential polypeptide synthesis of the proton-translocating ATPase of Escherichia coli.

Authors:  W S Brusilow; D J Klionsky; R D Simoni
Journal:  J Bacteriol       Date:  1982-09       Impact factor: 3.490

8.  Nucleotide sequence of the Rhodospirillum rubrum atp operon.

Authors:  G Falk; A Hampe; J E Walker
Journal:  Biochem J       Date:  1985-06-01       Impact factor: 3.857

9.  Bacillus subtilis F0F1 ATPase: DNA sequence of the atp operon and characterization of atp mutants.

Authors:  M Santana; M S Ionescu; A Vertes; R Longin; F Kunst; A Danchin; P Glaser
Journal:  J Bacteriol       Date:  1994-11       Impact factor: 3.490

10.  Comparative genome analysis of "Candidatus Phytoplasma australiense" (subgroup tuf-Australia I; rp-A) and "Ca. Phytoplasma asteris" Strains OY-M and AY-WB.

Authors:  L T T Tran-Nguyen; M Kube; B Schneider; R Reinhardt; K S Gibb
Journal:  J Bacteriol       Date:  2008-03-21       Impact factor: 3.490

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