Literature DB >> 9665704

Electron transfer kinetics during the reduction and turnover of the cytochrome caa3 complex from Bacillus subtilis.

M Assempour1, D Lim, B C Hill.   

Abstract

The cytochrome caa3 complex from Bacillus subtilis is a member of the cytochrome oxidase superfamily of respiratory enzyme complexes. The key difference in the cytochrome caa3 complex lies in the addition of a domain, homologous with mitochondrial cytochrome c, that is fused to the C-terminal end of its subunit II. Measurements of steady-state and transient reduction kinetics have been carried out on the cytochrome caa3 complex. Reduction of the cyanide-bound enzyme with ascorbate and N,N,N',N'-tetramethyl-p-phenylenediamine (TMPD) supports a sequence of electron transfer in which cytochromec is reduced initially, and this is followed by rapid internal electron transfer from cytochrome c to CuA and from CuA to cytochrome a. Steady-state kinetics with exogenous cytochrome c as the substrate demonstrates the capability of the cytochrome caa3 complex to act as a cytochrome c oxidase. The cytochrome c from B. subtilis is the most efficient cytochrome c of those tested. Steady-state kinetics with ascorbate-TMPD as the reductant, in the absence of exogenous cytochrome c, reveals a biphasic pattern even though only a single, covalent cytochrome c interaction site is present. The two-phase kinetics are characterized by a low activity phase associated with a high apparent affinity for TMPD and a high activity phase with a low affinity for TMPD. This pattern is observed over a wide range of ionic strengths and enzyme concentrations, and with both purified and membrane extract forms of cytochrome caa3. It is proposed that the biphasic steady-state kinetics of this oxidase, and other members of the cytochrome oxidase superfamily, do not result directly from different interactions with cytochrome c but are due to a change in the redox kinetics within the centers of the conventional oxidase unit itself. Our results will be related to models that account for the biphasic steady-state kinetics exhibited by cytochrome oxidase.

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Year:  1998        PMID: 9665704     DOI: 10.1021/bi980331c

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  4 in total

1.  Product-controlled steady-state kinetics between cytochrome aa(3) from Rhodobacter sphaeroides and equine ferrocytochrome c analyzed by a novel spectrophotometric approach.

Authors:  Myat T Lin; Robert B Gennis
Journal:  Biochim Biophys Acta       Date:  2012-04-06

2.  Biochemical and biophysical characterization of the two isoforms of cbb3-type cytochrome c oxidase from Pseudomonas stutzeri.

Authors:  Hao Xie; Sabine Buschmann; Julian D Langer; Bernd Ludwig; Hartmut Michel
Journal:  J Bacteriol       Date:  2013-11-08       Impact factor: 3.490

3.  Structure of the cytochrome aa 3 -600 heme-copper menaquinol oxidase bound to inhibitor HQNO shows TM0 is part of the quinol binding site.

Authors:  Jingjing Xu; Ziqiao Ding; Bing Liu; Sophia M Yi; Jiao Li; Zhengguang Zhang; Yuchen Liu; Jin Li; Liu Liu; Aiwu Zhou; Robert B Gennis; Jiapeng Zhu
Journal:  Proc Natl Acad Sci U S A       Date:  2019-12-30       Impact factor: 11.205

4.  Heme O synthase and heme A synthase from Bacillus subtilis and Rhodobacter sphaeroides interact in Escherichia coli.

Authors:  Brienne M Brown; Zhihong Wang; Kenneth R Brown; Julia A Cricco; Eric L Hegg
Journal:  Biochemistry       Date:  2004-10-26       Impact factor: 3.162

  4 in total

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