Quenching of excited states of chlorophyll molecules in submembrane fractions of Photosystem I by exogenous quinones

Abstract

The ability of three substituted quinones, 2,5-dibromo-3-methyl-6-isopropyl- p-benzoquinone (DBMIB), 2,6-dichloro- p-benzoquinone (DCBQ), and tetramethyl- p-benzoquinone (duriquinone) to quench the excited states of chlorophyll (Chl) molecules in Photosystem I (PSI) was studied. Chl fluorescence emission measured with isolated PSI submembrane fractions was reduced following the addition of exogenous quinones. This quenching progressively increased with rising concentrations of the exogenous quinones according to the Stern–Volmer law. The values of Stern–Volmer quenching coefficients were found to be 3.28×10 5 M −1 (DBMIB), 1.31×10 4 M −1 (DCBQ), and 3.7×10 3 M −1 (duroquinone). The relative quenching capacities of the various exogenous quinones in PSI thus strictly coincided to those found for the quenching of Fo level of Chl fluorescence in isolated thylakoids, which is emitted largely by Photosystem II (PSII) [Biochim. Biophys. Acta (2003) 1604, 115–123]. Quenching of Chl excited states in PSI submembrane fractions by exogenous quinones slowed down the rate of P700, primary electron donor of PSI, photooxidation measured at limiting actinic light irradiances thus revealing a reduced photochemical capacity of absorbed quanta. The possible involvement of non-photochemical quenching of excited Chl states by oxidized phylloquinones, electron acceptors of PSI, and oxidized plastoquinones, mobile electron carriers between PSII and the cytochrome b 6/ f complex, into the control of photochemical activity of PSI is discussed.