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A role for cytochrome c and cytochrome c peroxidase in electron shuttling from Erv1
Author(s) -
Dabir Deepa V,
Leverich Edward P,
Kim SungKun,
Tsai Frederick D,
Hirasawa Masakazu,
Knaff David B,
Koehler Carla M
Publication year - 2007
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1038/sj.emboj.7601909
Subject(s) - cytochrome c peroxidase , cytochrome , cytochrome c , cytochrome p450 reductase , cytochrome c oxidase , biology , cytochrome c1 , cytochrome b6f complex , electron transport chain , biochemistry , redox , coenzyme q – cytochrome c reductase , chemistry , cytochrome b , enzyme , mitochondrion , gene , mitochondrial dna , organic chemistry
Erv1 is a flavin‐dependent sulfhydryl oxidase in the mitochondrial intermembrane space (IMS) that functions in the import of cysteine‐rich proteins. Redox titrations of recombinant Erv1 showed that it contains three distinct couples with midpoint potentials of −320, −215, and −150 mV. Like all redox‐active enzymes, Erv1 requires one or more electron acceptors. We have generated strains with erv1 conditional alleles and employed biochemical and genetic strategies to facilitate identifying redox pathways involving Erv1. Here, we report that Erv1 forms a 1:1 complex with cytochrome c and a reduced Erv1 can transfer electrons directly to the ferric form of the cytochrome. Erv1 also utilized molecular oxygen as an electron acceptor to generate hydrogen peroxide, which is subsequently reduced to water by cytochrome c peroxidase (Ccp1). Oxidized Ccp1 was in turn reduced by the Erv1‐reduced cytochrome c . By coupling these pathways, cytochrome c and Ccp1 function efficiently as Erv1‐dependent electron acceptors. Thus, we propose that Erv1 utilizes diverse pathways for electron shuttling in the IMS.