Abstract
Abstract—The characterization and kinetic analysis by laser Rash photolysis of an improved model system for observing chlorophyllaphotosensitized electron transfer across a lipid bilayer membrane is described. In this system, the electron acceptor is a water‐soluble naphthoquinone, S‐(2‐methyl‐l,4‐naphthoquinonyl‐3)‐glutathione (MGNQ) which is dissolved in the inner aqueous compartments of phospholipid bilayer vesicles, and the electron donor is glutathione (GSH) which is dissolved in the outer aqueous phase. Chlorophyll (Chl) is dissolved in the membrane. Oxidative quenching of the triplet state of Chl by the quinone at the inner surface of the vesicle produces the Chl+and MGNQradicals. Chi+is reduced by GSH at the outer surface of the vesicle (k= 2.6 × 106M‐1s‐1) in competition with the recombination between Chl+. and MGNO(k= 2.5 × 103S‐1). It is shown that a kinetic mechanism involving competition between recombination, electron transfer across the bilayer, and reduction by donor at the opposite surface can quantitatively account for the decay of Chl+. Electron transport across the bilayer is postulated to occur by a two‐step mechanism involving electron exchange between Chl and Chl+within the lipid monolayer (k= 3.2 × 106M‐1s‐1) and across the bilayer. The rate constant for the latter exchange process approaches 104s‐1as the concentration of Chl in the bilayer increases. Under appropriate conditions, approximately 20% of all photons absorbed by the vesicle system result in electron transfer across the mcmbrane from GSH to MGNQ.

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