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

Ilya Belevich, Vitaliy B. Borisov, Jie Zhang, Ke Yang, Alexander A. Konstantinov, Robert B. Gennis, Michael I. Verkhovsky

Research output: Contribution to journalArticle

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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+, b 595 3+, 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.

Original languageEnglish (US)
Pages (from-to)3657-3662
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume102
Issue number10
DOIs
StatePublished - Mar 8 2005
Externally publishedYes

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Cytochromes
Heme
Protons
Catalytic Domain
Electrons
Oxidation-Reduction
Enzymes
Dithionite
Photolysis
Reducing Agents
Carbon Monoxide
Membrane Potentials
heme d
Oxidoreductases
heme b(595)
Oxygen
Escherichia coli

Keywords

  • Electron transfer reactions
  • Oxidase
  • Respiratory chain

ASJC Scopus subject areas

  • General

Cite this

Time-resolved electrometric and optical studies on cytochrome bd suggest a mechanism of electron-proton coupling in the di-heme active site. / Belevich, Ilya; Borisov, Vitaliy B.; Zhang, Jie; Yang, Ke; Konstantinov, Alexander A.; Gennis, Robert B.; Verkhovsky, Michael I.

In: Proceedings of the National Academy of Sciences of the United States of America, Vol. 102, No. 10, 08.03.2005, p. 3657-3662.

Research output: Contribution to journalArticle

Belevich, Ilya ; Borisov, Vitaliy B. ; Zhang, Jie ; Yang, Ke ; Konstantinov, Alexander A. ; Gennis, Robert B. ; Verkhovsky, Michael I. / Time-resolved electrometric and optical studies on cytochrome bd suggest a mechanism of electron-proton coupling in the di-heme active site. In: Proceedings of the National Academy of Sciences of the United States of America. 2005 ; Vol. 102, No. 10. pp. 3657-3662.
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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.

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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+, b 595 3+, 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 (b558 2+, b595 2+, d 2+) and E445A mutant oxidase (b558 2+, b 595 3+, 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.

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KW - Respiratory chain

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