Literature DB >> 2834226

Protonic sidedness of the binuclear iron-copper centre in cytochrome oxidase.

M Wikström1.   

Abstract

The oxidised (ferric-cupric) binuclear centre of cytochrome oxidase is converted into two other states, presumably ferrylcupric (F) and ferric-peroxy-cupric (P), by energy-dependent reversed electron transfer from the centre (and water) to cytochrome c [(1981) Proc. Natl. Acad. Sci. USA 78, 4051-4054; (1987) Chem. Scr. 27B, 53-58]. This sequence of events represents a partial reversal of the O2 reduction catalysed by the centre. Here it is shown that the strong pH-dependence of these reactions is exerted specifically from the matrix (M) side of the inner mitochondrial membrane. This proves unequivocally that the binuclear centre generates protonmotive force by means of its vectorial accessibility for electrons and protons.

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Year:  1988        PMID: 2834226     DOI: 10.1016/0014-5793(88)80741-5

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  3 in total

1.  The roles of the two proton input channels in cytochrome c oxidase from Rhodobacter sphaeroides probed by the effects of site-directed mutations on time-resolved electrogenic intraprotein proton transfer.

Authors:  A A Konstantinov; S Siletsky; D Mitchell; A Kaulen; R B Gennis
Journal:  Proc Natl Acad Sci U S A       Date:  1997-08-19       Impact factor: 11.205

2.  Proton-dependent electron transfer from CuA to heme a and altered EPR spectra in mutants close to heme a of cytochrome oxidase.

Authors:  Denise A Mills; Shujuan Xu; Lois Geren; Carrie Hiser; Ling Qin; Martyn A Sharpe; John McCracken; Bill Durham; Francis Millett; Shelagh Ferguson-Miller
Journal:  Biochemistry       Date:  2008-10-11       Impact factor: 3.162

Review 3.  The histidine cycle: a new model for proton translocation in the respiratory heme-copper oxidases.

Authors:  J E Morgan; M I Verkhovsky; M Wikström
Journal:  J Bioenerg Biomembr       Date:  1994-12       Impact factor: 2.945

  3 in total

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