Time-resolved electrometric and optical studies on cytochrome bd suggest a mechanism of electron-proton coupling in the di-heme active site.

@article{citeulike:113064, abstract = {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 (b558(2+), b595(2+), d(2+)) and E445A mutant oxidase (b558(2+), b595(3+), d(2+)) bind O2 rapidly, but formation of the oxoferryl state in the mutant is approximately 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 (b595, d) upon its full reduction by two electrons.}, address = {Helsinki Bioenergetics Group, Institute of Biotechnology, University of Helsinki, PB 65 (Viikinkaari 1), FIN-00014, Helsinki, Finland; A. N. Belozersky Institute of Physico-Chemical Biology, Moscow State University, Moscow 119992, Russia.}, author = {Belevich, Ilya and Borisov, Vitaliy B B. and Zhang, Jie and Yang, Ke and Konstantinov, Alexander A A. and Gennis, Robert B B. and Verkhovsky, Michael I I. }, citeulike-article-id = {113064}, doi = {http://dx.doi.org/10.1073/pnas.0405683102}, issn = {0027-8424}, journal = {Proc Natl Acad Sci U S A}, keywords = {cytochrome}, month = {February}, posted-at = {2005-03-03 12:44:50}, priority = {2}, title = {Time-resolved electrometric and optical studies on cytochrome bd suggest a mechanism of electron-proton coupling in the di-heme active site.}, url = {http://dx.doi.org/10.1073/pnas.0405683102}, year = {2005} }

TY - JOUR ID - citeulike:113064 L3 - citeulike-article-id:113064 TI - Time-resolved electrometric and optical studies on cytochrome bd suggest a mechanism of electron-proton coupling in the di-heme active site. JF - Proc Natl Acad Sci U S A AD - Helsinki Bioenergetics Group, Institute of Biotechnology, University of Helsinki, PB 65 (Viikinkaari 1), FIN-00014, Helsinki, Finland; A. N. Belozersky Institute of Physico-Chemical Biology, Moscow State University, Moscow 119992, Russia. SN - 0027-8424 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 (b558(2+), b595(2+), d(2+)) and E445A mutant oxidase (b558(2+), b595(3+), d(2+)) bind O2 rapidly, but formation of the oxoferryl state in the mutant is approximately 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 (b595, d) upon its full reduction by two electrons. KW - cytochrome 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 - 2005/02/22/ UR - http://dx.doi.org/10.1073/pnas.0405683102 ER -