Spectral and redox characterization of the heme ci of the cytochrome b6f complex.

ABSTRACT: Absorption spectra of the purified cytochrome b(6)f complex from Chlamydomonas reinhardtii were monitored as a function of the redox potential. Four spectral and redox components were identified: in addition to heme f and the two b hemes, the fourth component must be the new heme c(i) (also denoted x) recently discovered in the crystallographic structures. This heme is covalently attached to the protein, but has no amino acid axial ligand. It is located in the plastoquinone-reducing site Q(i) in the immediate vicinity of a b heme. Each heme titrated as a one-electron Nernst curve, with midpoint potentials at pH 7.0 of -130 mV and -35 mV (hemes b), +100 mV (heme c(i)), and +355 mV (heme f). The reduced minus oxidized spectrum of heme c(i) consists of a broad absorption increase centered app

SUBMITTER: Alric J 

PROVIDER: S-EPMC1276102 | biostudies-literature | 2005 Nov

REPOSITORIES: biostudies-literature