Inverted region in the reaction of the quinone reduction in the A1-site of photosystem I from cyanobacteria.

Abstract

Photosystem I from the menB strain of Synechocystis sp. PCC 6803 containing foreign quinones in the A1 sites was used for studying the primary steps of electron transfer by pump-probe femtosecond laser spectroscopy. The free energy gap (- ΔG) of electron transfer between the reduced primary acceptor A0 and the quinones bound in the A1 site varied from 0.12eV for the low-potential 1,2-diamino-anthraquinone to 0.88eV for the high-potential 2,3-dichloro-1,4-naphthoquinone, compared to 0.5eV for the native phylloquinone. It was shown that the kinetics of charge separation between the special pair chlorophyll P700 and the primary acceptor A0 was not affected by quinone substitutions, whereas the rate of A0 → A1 electron transfer was sensitive to the redox-potential of quinones: the decrease of - ΔG by 400meV compared to the native phylloquinone resulted in a ~ fivefold slowing of the reaction The presence of the asymmetric inverted region in the ΔG dependence of the reaction rate indicates that the electron transfer in photosystem I is controlled by nuclear tunneling and should be treated in terms of quantum electron-phonon interactions. A three-mode implementation of the multiphonon model, which includes modes around 240cm-1 (large-scale protein vibrations), 930cm-1 (out-of-plane bending of macrocycles and protein backbone vibrations), and 1600cm-1 (double bonds vibrations) was applied to rationalize the observed dependence. The modes with a frequency of at least 1600cm-1 make the predominant contribution to the reorganization energy, while the contribution of the "classical" low-frequency modes is only 4%.