TY - JOUR
T1 - Time-resolved electrometric and optical studies on cytochrome bd suggest a mechanism of electron-proton coupling in the di-heme active site
AU - Belevich, Ilya
AU - Borisov, Vitaliy B.
AU - Zhang, Jie
AU - Yang, Ke
AU - Konstantinov, Alexander A.
AU - Gennis, Robert B.
AU - Verkhovsky, Michael I.
PY - 2005/3/8
Y1 - 2005/3/8
N2 - Time-resolved electron transfer and electrogenic H+ translocation have been compared in a bd-type quinol oxidase from Escherichia coli and its E445A mutant. The high-spin heme b595 is found to be retained by the enzyme in contrast to the original proposal, but it is not reducible even by excess of dithionite. When preincubated with the reductants, both the WT (b5582+, b5952+, d 2+) and E445A mutant oxidase (b5582+, b 5953+, d2+) bind O2 rapidly, but formation of the oxoferryl state in the mutant is ≈100-fold slower than in the WT enzyme. At the same time, the E445A substitution does not affect intraprotein electron re-equilibration after the photolysis of CO bound to ferrous heme d in the one-electron-reduced enzyme (the so-called "electron backflow"). The backflow is coupled to membrane potential generation. Electron transfer between hemes d and b558 is electrogenic. In contrast, electron transfer between hemes d and b595 is not electrogenic, although heme b595 is the major electron acceptor for heme d during the backflow, and therefore is not likely to be accompanied by net H+ uptake or release. The E445A replacement does not alter electron distribution between hemes b595 and d in the one-electron reduced cytochrome bd [Em(d) > Em(b595), where Em is the midpoint redox potential]; however, it precludes reduction of heme b595, given heme d has been reduced already by the first electron. Presumably, E445 is one of the two redox-linked ionizable groups required for charge compensation of the di-heme oxygen-reducing site (b 595, d) upon its full reduction by two electrons.
AB - Time-resolved electron transfer and electrogenic H+ translocation have been compared in a bd-type quinol oxidase from Escherichia coli and its E445A mutant. The high-spin heme b595 is found to be retained by the enzyme in contrast to the original proposal, but it is not reducible even by excess of dithionite. When preincubated with the reductants, both the WT (b5582+, b5952+, d 2+) and E445A mutant oxidase (b5582+, b 5953+, d2+) bind O2 rapidly, but formation of the oxoferryl state in the mutant is ≈100-fold slower than in the WT enzyme. At the same time, the E445A substitution does not affect intraprotein electron re-equilibration after the photolysis of CO bound to ferrous heme d in the one-electron-reduced enzyme (the so-called "electron backflow"). The backflow is coupled to membrane potential generation. Electron transfer between hemes d and b558 is electrogenic. In contrast, electron transfer between hemes d and b595 is not electrogenic, although heme b595 is the major electron acceptor for heme d during the backflow, and therefore is not likely to be accompanied by net H+ uptake or release. The E445A replacement does not alter electron distribution between hemes b595 and d in the one-electron reduced cytochrome bd [Em(d) > Em(b595), where Em is the midpoint redox potential]; however, it precludes reduction of heme b595, given heme d has been reduced already by the first electron. Presumably, E445 is one of the two redox-linked ionizable groups required for charge compensation of the di-heme oxygen-reducing site (b 595, d) upon its full reduction by two electrons.
KW - Electron transfer reactions
KW - Oxidase
KW - Respiratory chain
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U2 - 10.1073/pnas.0405683102
DO - 10.1073/pnas.0405683102
M3 - Article
C2 - 15728392
AN - SCOPUS:14844351539
SN - 0027-8424
VL - 102
SP - 3657
EP - 3662
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 10
ER -