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Mitochondrial cytochrome c oxidase: catalysis, coupling and controversies
Author(s) -
Peter R. Rich
Publication year - 2017
Publication title -
biochemical society transactions
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.562
H-Index - 144
eISSN - 1470-8752
pISSN - 0300-5127
DOI - 10.1042/bst20160139
Subject(s) - catalytic cycle , cytochrome c oxidase , chemistry , mechanism (biology) , mitochondrion , inner mitochondrial membrane , coupling (piping) , catalysis , oxidase test , biochemistry , biophysics , biology , enzyme , physics , materials science , quantum mechanics , metallurgy
Mitochondrial cytochrome c oxidase is a member of a diverse superfamily of haem-copper oxidases. Its mechanism of oxygen reduction is reviewed in terms of the cycle of catalytic intermediates and their likely chemical structures. This reaction cycle is coupled to the translocation of protons across the inner mitochondrial membrane in which it is located. The likely mechanism by which this occurs, derived in significant part from studies of bacterial homologues, is presented. These mechanisms of catalysis and coupling, together with current alternative proposals of underlying mechanisms, are critically reviewed.

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