Abstract

The dependence of PSII triplet populations as a function of the primary quinone acceptor Q A redox state has been investigated by means of the fluorescence detected magnetic resonance (FDMR) technique in isolated thylakoid membranes. The results show that the population level of a microsecond decaying component having zero field splitting parameters | D |=0.0292 cm −1 and | E |=0.0037 cm −1 is inversely correlated to that of the recombination triplet (| D |=0.0285 cm −1 | E |=0.045 cm −1 ). The results could be interpreted in terms of the fast (50–150 μs) decaying population being either the recombination triplet when the primary quinone Q A is singly reduced or a triplet located on a chlorophyll which is in tight singlet transfer coupling with the primary donor.

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