Literature DB >> 12437359

Nuclear wave packet motion between P* and P(+)B(A)(-) potential surfaces with a subsequent electron transfer to H(A) in bacterial reaction centers at 90 K. Electron transfer pathway.

Andrei G Yakovlev1, Anatoli Ya Shkuropatov, Vladimir A Shuvalov.   

Abstract

In Rhodobacter sphaeroides R-26 reaction centers (RCs) the nuclear wave packet induced by 25 fs excitation at 90 K moves on the primary electron donor P* potential energy hypersurface with initial frequency at approximately 130 cm(-1) (monitored by stimulated emission measurement). At the long-wavelength side of P* stimulated emission at 935 nm the wave packet is transferred to the surface with P(+)B(A)(-) character at 120, 380, 1.2 fs, etc. delays (monitored by measurement of the primary electron acceptor B(A)(-) band at 1020 nm). However, only beginning from 380 fs delay and later the relative stabilization of the state P(+)B(A)(-) is observed. This is accompanied by the electron transfer to bacteriopheophytin H(A) (monitored by H(A) band measurement at 760 nm). The most active mode of 32 cm(-1) in the electron transfer and its overtones up to the seventh were found in the Fourier transform spectrum of the oscillatory part of the kinetics of the P* stimulated emission and of the P(+)B(A)(-) and P(+)H(A)(-) formation. This mode and its overtones are apparently populated via the 130 cm(-1) vibrational mode. The deuteration of the sample shifts the fundamental frequency (32 cm(-1)) and all overtones by the same factor of approximately 1.3. This mode and its overtones are suppressed by a factor of approximately 4.7 in the dry film of RCs. The results obtained indicate that the 32 cm(-1) mode might be related to a rotation of hydrogen-containing groups (possibly the water molecule) participating in the modulation of the primary electron transfer from P* to B(A)(-) in at least 35% of RCs. The Brookhaven Protein Data Bank (1PRC) displays the water molecule located at the position HOH302 between His M200 (axial ligand for P(B)) and the oxygen of ring V of B(A) which might be a part (approximately 35%) of the molecular pathway for electron transfer from P* to B(A).

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Year:  2002        PMID: 12437359     DOI: 10.1021/bi020250n

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  9 in total

1.  Femtosecond absorption band formation at 1080 and 1020 nm as an indication of charge-separated states P(A)delta+ P7(B)delta- and p+ B(A)- in photosynthetic reaction centers of the purple bacterium Rhodobacter sphaeroides.

Authors:  R A Khatypov; A Yu Khmelnitskiy; A M Khristin; V A Shuvalov
Journal:  Dokl Biochem Biophys       Date:  2010 Jan-Feb       Impact factor: 0.788

2.  Coherent electron transfer in the primary act of bacterial photosynthesis: a model based on Redfield theory.

Authors:  V I Novoderezhkin; A G Yakovlev; V A Shuvalov
Journal:  Dokl Biochem Biophys       Date:  2005 May-Jun       Impact factor: 0.788

3.  Primary charge separation in the reaction centers of Rhodobacter sphaeroides mutants L153HY and L153HY+M182HL.

Authors:  R A Khatypov; A Yu Khmelnitsky; M M Leonova; L G Vasilyeva; V A Shuvalov
Journal:  Dokl Biochem Biophys       Date:  2008 Sep-Oct       Impact factor: 0.788

Review 4.  Primary light-energy conversion in tetrameric chlorophyll structure of photosystem II and bacterial reaction centers: I. A review.

Authors:  Ravil A Khatypov; Anton Yu Khmelnitskiy; Maria M Leonova; Lyudmila G Vasilieva; Vladimir A Shuvalov
Journal:  Photosynth Res       Date:  2008-10-14       Impact factor: 3.573

Review 5.  A new look on the formation and interaction of elementary particles in atoms and molecules including photoreaction centers.

Authors:  V A Shuvalov
Journal:  Photosynth Res       Date:  2008-11-05       Impact factor: 3.573

6.  Spectral exhibition of electron-vibrational relaxation in P* state of Rhodobacter sphaeroides reaction centers.

Authors:  Andrei G Yakovlev; Vladimir A Shuvalov
Journal:  Photosynth Res       Date:  2014-09-21       Impact factor: 3.573

7.  Mutation H(M202)L does not lead to the formation of a heterodimer of the primary electron donor in reaction centers of Rhodobacter sphaeroides when combined with mutation I(M206)H.

Authors:  Anton M Khristin; Alexey A Zabelin; Tatiana Yu Fufina; Ravil A Khatypov; Ivan I Proskuryakov; Vladimir A Shuvalov; Anatoly Ya Shkuropatov; Lyudmila G Vasilieva
Journal:  Photosynth Res       Date:  2020-03-03       Impact factor: 3.573

8.  Photosynthetic reaction center variants made via genetic code expansion show Tyr at M210 tunes the initial electron transfer mechanism.

Authors:  Jared Bryce Weaver; Chi-Yun Lin; Kaitlyn M Faries; Irimpan I Mathews; Silvia Russi; Dewey Holten; Christine Kirmaier; Steven G Boxer
Journal:  Proc Natl Acad Sci U S A       Date:  2021-12-21       Impact factor: 12.779

9.  Coherent intradimer dynamics in reaction centers of photosynthetic green bacterium Chloroflexus aurantiacus.

Authors:  Andrei G Yakovlev; Vladimir A Shuvalov
Journal:  Sci Rep       Date:  2020-01-14       Impact factor: 4.379

  9 in total

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