Excited chlorophyll and related problems.

A historical outline is presented of the primary light energy conversion in photosynthesis studied by our research group. We found that photoexcited chlorophylls, pheophytins and porphyrins are capable of reversible and irreversible oxido-reduction. The mechanism of the photosensitized electron transfer from donor to acceptor molecule is based on the reversible photochemical oxido-reduction of the pigment-sensitizer. This property of the excited pigments is realized in the reaction centres of photosynthetic cells when photooxidation of bacteriochlorophyll(s) or chlorophyll of Photosystem II is coupled to pheophytin reduction leading to the final charge separation.The studies of the state and function of pigments in the course of chlorophyll biosynthesis in cellular and non-cellular systems revealed different monomeric and aggregated forms of pigments and the phenomenon of self-assembly of various forms of chlorophylls, bacteriochlorophylls and protochlorophylls. The discovery of protochlorophyll photoreduction in non-cellular system allowed the study of the molecular mechanisms of this reaction.In order to construct models of photosynthetic charge separation, we used inorganic photocatalysts-semiconductors, mainly titanium dioxide, and pigments incorporated into detergent micelles or lipid vesicles. To prevent back reactions we used heterogeneous systems where primary unstable products were spatially separated; coupling of solubilized chlorophylls or semiconductor particles with bacterial hydrogenase led to molecular hydrogen photoproduction. Light excitation of some coenzymes, mainly NADH and NADPH, was considered from the point of view of early events of chemical evolution.Now we are interested in the creation of photobiochemical systems using principles of photosynthesis for the conversion and storage of solar energy.