J. Bernarding et al., KINETIC-STUDIES ON THE STABILIZATION OF THE PRIMARY RADICAL PAIR P680(-) IN DIFFERENT PHOTOSYSTEM-II PREPARATIONS FROM HIGHER-PLANTS() PHEO(), Photochemistry and photobiology, 59(5), 1994, pp. 566-573
The stabilization of the primary radical pair P680(+) pheophytin (Pheo
)(-) through rapid electron transfer from Pheo(-) to the special plast
oquinone of photosystem II (PS II), Q(A), was analyzed on the basis of
time-resolved (40 ps) UV-absorption changes detected in different PS
II preparations from higher plants. Lifetime measurements of (1)Chl f
luorescence by single photon counting and a numerical analysis of the
redox reactions revealed (1) at exciton densities required for light s
aturation of the stable charge separation, annihilation processes domi
nate the excited state decay leading to very similar lifetimes of (1)C
hl in systems with open and closed reaction centers and (2) the diffe
rence of absorption changes induced by actinic flashes of comparativel
y high photon density in samples with open and photochemically closed
reaction centers, respectively, provides a suitable measure of the rat
e constant of Q(A)(-) formation. Conclusion 2 was confirmed in PS II m
embrane fragments by measurements at three wavelengths (280 nm, 292 nm
and 325 nm) where the difference spectrum of Q(A)(-) formation exhibi
ts characteristic features. The numerical evaluation of the experiment
al data led to the following results: (1) the rate constant of Q(A)(-)
formation was found to be (300 +/- 100 ps)(-1) in PS II membrane frag
ments and PS II core complexes deprived of the distal and proximal ant
enna and (2) an iron depletion treatment of membrane fragments does no
t affect these kinetics. The implications of these results are briefly
discussed in terms of the PS II reaction pattern.