Literature DB >> 16475794

Triplet-state conformational changes in 15-cis-spheroidene bound to the reaction center from Rhodobacter sphaeroides 2.4.1 as revealed by time-resolved EPR spectroscopy: strengthened hypothetical mechanism of triplet-energy dissipation.

Yoshinori Kakitani1, Ritsuko Fujii, Yasushi Koyama, Hiroyoshi Nagae, Lee Walker, Bruce Salter, Alexander Angerhofer.   

Abstract

Time-resolved EPR spectra of 15-cis-spheroidene bound to the reaction center from Rhodobacter sphaeroides 2.4.1 were recorded at low temperatures. (1) A three-component analysis of the spectral-data matrices by singular-value decomposition followed by global fitting identified the transformation of the triplet carotenoid, (3)Car(I) --> (3)Car(II); during this process, the leak of the triplet population was suggested. A four-component analysis suggested the presence of a representative intermediate, (3)Car(R), that forms a leak channel of the triplet population. (2) A theoretical calculation of the zero-field splitting parameters, |D| and |E|, by the use of a polyene model, showed that the transformation, (3)Car(I) --> (3)Car(R) --> (3)Car(II), accompanies the conformational changes of (0 degrees , 0 degrees , 0 degrees ) --> (+20 degrees , -20 degrees , +20 degrees ) --> (+45 degrees , -40 degrees , +40 degrees ) around the central cis C15=C15', trans C13=C14, and trans C11=C12 bonds, respectively. (3) The initial, rapid decrease followed by the inversion of spin polarization along the z axis of (3)Car was observed, which was correlated with a change in the spin angular momentum. (4) In reference to the binding pocket of the Car, determined by X-ray crystallography, the conformational changes were ascribed to the intrinsic isomerization property of 15-cis (3)Car as well as the Car-peptide intermolecular interaction; a detailed picture was proposed. All of the above results support the mechanism of triplet-energy dissipation proposed previously: the rotational motions around the central double bonds cause a change in the orbital angular momentum and, through the spin-orbit coupling, a change in the spin angular momentum, which enhances the T(1) --> S(0) intersystem crossing dissipating the triplet energy.

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Year:  2006        PMID: 16475794     DOI: 10.1021/bi0511538

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


  5 in total

1.  Two stereoisomers of spheroidene in the Rhodobacter sphaeroides R26 reaction center: a DFT analysis of resonance Raman spectra.

Authors:  A C Wirtz; M C van Hemert; J Lugtenburg; H A Frank; E J J Groenen
Journal:  Biophys J       Date:  2007-08-01       Impact factor: 4.033

2.  Tracking Equilibrium and Nonequilibrium Shifts in Data with TREND.

Authors:  Jia Xu; Steven R Van Doren
Journal:  Biophys J       Date:  2017-01-24       Impact factor: 4.033

3.  Action Spectroscopy on Dense Samples of Photosynthetic Reaction Centers of Rhodobacter sphaeroides WT Based on Nanosecond Laser-Flash C Photo-CIDNP MAS NMR.

Authors:  Eugenio Daviso; Anna Diller; Peter Gast; A Alia; Johan Lugtenburg; Marc G Müller; Jörg Matysik
Journal:  Appl Magn Reson       Date:  2009-12-03       Impact factor: 0.831

4.  Photoprotection in intact cells of photosynthetic bacteria: quenching of bacteriochlorophyll fluorescence by carotenoid triplets.

Authors:  Gábor Sipka; Péter Maróti
Journal:  Photosynth Res       Date:  2017-10-24       Impact factor: 3.573

5.  Low-temperature pulsed EPR study at 34 GHz of the triplet states of the primary electron Donor P865 and the carotenoid in native and mutant bacterial reaction centers of Rhodobacter sphaeroides.

Authors:  Aliaksandr Marchanka; Mark Paddock; Wolfgang Lubitz; Maurice van Gastel
Journal:  Biochemistry       Date:  2007-12-04       Impact factor: 3.162

  5 in total

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