The dependence of the initial electron-transfer rate on driving force in Rhodobacter sphaeroides reaction centers

Arlene L M Haffa, Su Lin, Evaldas Katilius, JoAnn C. Williams, Aileen K W Taguchi, James Paul Allen, Neal W. Woodbury

Research output: Contribution to journalArticle

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Abstract

The kinetics of the primary electron transfer following excitation of the bacteriochlorophyll dimer (P) to its lowest excited singlet state were determined for a series of reaction center mutants of Rhodobacter sphaeroides that have P/P+ midpoint potentials 44-147 mV below wild type. These strains were capable of photosynthetic growth and had normal bacteriochlorophyll-to-bacteriopheophytin ratios. Decreasing the P/P+ midpoint potential resulted in an increase in the rate constant of initial electron transfer in each of the mutants tested. At room temperature, the fastest electron-transfer time constant observed was 1.8 ps from a mutant with a midpoint potential 127 mV below wild type. The dependence of the rate on driving force in these measurements and in previous measurements of mutants with high P/P+ midpoint potentials at room temperature was fit to a Marcus equation. Wild type was displaced approximately 100 meV from the peak of this curve. This analysis yielded a reorganization energy between 180 and 380 meV and an electronic coupling between 28 and 33 cm-1 depending on what value is assumed for the standard reaction free energy of initial charge separation in wild-type reaction centers. However, the temperature dependence of both wild type and the high midpoint potential mutant reaction centers is much weaker than that expected from the activation energy predicted by the Marcus formalism. In fact, an activation energy of at least 15 meV is predicted for wild type which should completely prevent electron transfer at cryogenic temperatures, yet the rate constant of initial electron transfer is increased at 10 K. One explanation for this is that certain vibrational modes that promote electron transfer in the reaction center are coupled to light absorption and are not in thermal equilibrium with the surrounding bath on the time scale of electron transfer. Thus, part of the vibrational energy required for rapid initial electron transfer may come from the absorbed photon rather than from the surrounding bath.

Original languageEnglish
Pages (from-to)7376-7384
Number of pages9
JournalJournal of Physical Chemistry B
Volume106
Issue number29
DOIs
Publication statusPublished - Jul 25 2002

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electron transfer
Electrons
Bacteriochlorophylls
baths
Rate constants
Activation energy
activation energy
Temperature
room temperature
polarization (charge separation)
cryogenic temperature
electromagnetic absorption
Excited states
Dimers
Cryogenics
Light absorption
Free energy
time constant
excitation
vibration mode

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry

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The dependence of the initial electron-transfer rate on driving force in Rhodobacter sphaeroides reaction centers. / Haffa, Arlene L M; Lin, Su; Katilius, Evaldas; Williams, JoAnn C.; Taguchi, Aileen K W; Allen, James Paul; Woodbury, Neal W.

In: Journal of Physical Chemistry B, Vol. 106, No. 29, 25.07.2002, p. 7376-7384.

Research output: Contribution to journalArticle

Haffa, Arlene L M ; Lin, Su ; Katilius, Evaldas ; Williams, JoAnn C. ; Taguchi, Aileen K W ; Allen, James Paul ; Woodbury, Neal W. / The dependence of the initial electron-transfer rate on driving force in Rhodobacter sphaeroides reaction centers. In: Journal of Physical Chemistry B. 2002 ; Vol. 106, No. 29. pp. 7376-7384.
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