Literature DB >> 6446901

Role of the subunits of the energy-transducing adenosine triphosphatase from Micrococcus lysodeikticus membranes studied by proteolytic digestion and immunological approaches.

F Mollinedo, V Larraga, F J Coll, E Muñoz.   

Abstract

An energy-transducing adenosine triphosphatase (ATPase, EC 3.6.1.3) that contains an extra polypeptide (delta) as well as three intrinsic subunits (alpha, beta, gamma) was purified from Micrococcus lysodeikticus membranes. The apparent subunit stoichiometry of this soluble ATPase complex is alpha 3 beta 3 gamma delta. The functional role of the subunits was studied by correlating subunit sensitivity to trypsin and effect of antibodies raised against holo-ATPase and its alpha, beta and gamma subunits with changes in ATPase activity and ATPase rebinding to membranes. A form of the ATPase with the subunit proportions 1.67(alpha):3.00(beta:0.17(gamma) was isolated after trypsin treatment of purified ATPase. This form has more than twice the specific activity of native enzyme. Other forms with less relative proportion of alpha subunits and absence of gamma subunit are not active. Of the antisera to subunits, only anti-(beta-subunit) serum shows a slight inhibitory effect on ATPase activity, but its combination with either anti-(alpha-subunit) or anti-(gamma-subunit) serum increases the effect. The results suggest that beta subunit is required for full ATPase activity, although a minor proportion of alpha and perhaps gamma subunit(s) is also required, probably to impart an active conformation to the protein. The additional polypeptide not hitherto described in Micrococcus lysodeikticus ATPase had a molecular weight of 20 000 and was found to be involved in ATPase binding to membranes. This 20 000-dalton component can be equated with the delta subunit of other energy-transducing ATPases and its association with the (alpha, beta, gamma) M. lysodeikticus ATPase complex appears to be dependent on bivalent cations. The present results do not preclude the possibility that the gamma subunit also plays a role in ATPase binding, in which, however, the major subunits do not seem to play a role.

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Year:  1980        PMID: 6446901      PMCID: PMC1161706          DOI: 10.1042/bj1860713

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  40 in total

1.  Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane.

Authors:  G Fairbanks; T L Steck; D F Wallach
Journal:  Biochemistry       Date:  1971-06-22       Impact factor: 3.162

2.  Membrane adenosine triphosphatase of Micrococcus lysodeikticus. Purification, properties of the "soluble" enzyme and properties of the membrane-bound enzyme.

Authors:  E Muñoz; M R Salton; M H Ng; M T Schor
Journal:  Eur J Biochem       Date:  1969-02

3.  Membrane-associated ATPase activity from Micrococcus lysodeikticus.

Authors:  E Munoz; J H Freer; D J Ellar; M R Salton
Journal:  Biochim Biophys Acta       Date:  1968-04-29

4.  Adenosinetriphosphatase of Micrococcus lysodeikticus: selective release and relationship to membrane structure.

Authors:  E Muñoz; M S Nachbar; M T Schor; M R Salton
Journal:  Biochem Biophys Res Commun       Date:  1968-08-13       Impact factor: 3.575

5.  An improved procedure for protein staining in polyacrylamide gels with a new type of Coomassie Brilliant Blue.

Authors:  W Diezel; G Kopperschläger; E Hofmann
Journal:  Anal Biochem       Date:  1972-08       Impact factor: 3.365

Review 6.  The structure of mitochondrial ATPase.

Authors:  A E Senior
Journal:  Biochim Biophys Acta       Date:  1973-12-31

7.  Partial resolution of the enzymes catalyzing photophosphorylation. 8. Properties of isolated subunits of coupling factor 1 from spinach chloroplasts.

Authors:  N Nelson; D W Deters; H Nelson; E Racker
Journal:  J Biol Chem       Date:  1973-03-25       Impact factor: 5.157

8.  Subunit structure and properties of two forms of adenosine triphosphatase released from Micrococcus lysodeikticus membranes.

Authors:  M R Salton; M T Schor
Journal:  Biochem Biophys Res Commun       Date:  1972-10-17       Impact factor: 3.575

9.  Molecular weight, amino acid composition and other properties of membrane-bound ATPase from Bacillus megaterium KM.

Authors:  R Mirsky; V Barlow
Journal:  Biochim Biophys Acta       Date:  1973-01-26

10.  Antibody to adenosine triphosphatase from membranes of Micrococcus lysodeikticus.

Authors:  T L Whiteside; M R Salton
Journal:  Biochemistry       Date:  1970-07-21       Impact factor: 3.162

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  7 in total

Review 1.  Evidence from immunological studies of structure-mechanism relationship of F1 and F1F0.

Authors:  D C Gautheron; C Godinot
Journal:  J Bioenerg Biomembr       Date:  1988-08       Impact factor: 2.945

2.  Characterization of monoclonal antibodies against mitochondrial F1-ATPase.

Authors:  M Moradi-Ameli; C Godinot
Journal:  Proc Natl Acad Sci U S A       Date:  1983-10       Impact factor: 11.205

3.  Structure of the mitochondrial F1 ATPase at 9-A resolution.

Authors:  L M Amzel; M McKinney; P Narayanan; P L Pedersen
Journal:  Proc Natl Acad Sci U S A       Date:  1982-10       Impact factor: 11.205

4.  Substructure of F1-ATPase (BF1 factor) from Micrococcus lysodeikticus. A cross-linking study with diimido esters.

Authors:  E Muñoz; P Palacios; A Marquet; J M Andreu
Journal:  Mol Cell Biochem       Date:  1980-12-10       Impact factor: 3.396

Review 5.  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

6.  Topography of the subunits of Micrococcus lysodeikticus F1-ATPase.

Authors:  A Mimbrera; L Rivas; F Mollinedo; E Muñoz; V Larraga
Journal:  Mol Cell Biochem       Date:  1983       Impact factor: 3.396

7.  Influence of the alpha-, beta- and gamma-subunits of the energy-transducing adenosine triphosphates from Micrococcus lysodeikticus in the immunochemical properties of the protein and in their reconstitution studied by a radioimmunoassay method.

Authors:  V Larraga; F Mollinedo; N Rubio; E Muñoz
Journal:  Biochem J       Date:  1981-03-01       Impact factor: 3.857

  7 in total

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