The excitation of bacterial reaction centers (RCs) at 870 nm by 30 fs pulse
s induces the nuclear wavepacket motions on the potential energy surface of
the primary electron donor excited state P*, which lead to the fs oscillat
ions in stimulated emission from P* [M.H. Vos, M.R. Jones, C.N. Hunter, J.
Breton, J.-C, Lambry and J.-L, Martin (1994) Biochemistry 33, 6750-6757] an
d in Q(Y) absorption band of the primary electron acceptor, bacteriochlorop
hyll monomer B-A [A.M. Streltsov, S.I.E. Vulto, A.Y. Shkuropatov, A.J. Hoff
, T.J. Aartsma and V.A. Shuvalov (1998) J. Phys. Chem. B 102, 7293-7298] wi
th a set of fundamental frequencies in the range of 10-300 cm(-1). We have
found that in pheophytin-modified RCs, the fs oscillations with frequency a
round 130 cm(-1) observed in the P*-stimulated emission as well as in the B
-A absorption band at 800 nm are accompanied by remarkable and reversible f
ormation of the 1020 nm absorption band which is characteristic of the radi
cal anion band of bacteriochlorophyll monomer B-A(-). These results are dis
cussed in terms of a reversible electron transfer between P* and B-A induce
d by a motion of the wavepacket near the intersection of potential energy s
urfaces of P* and P+BA-, when a maximal value of the Franck-Condon factor i
s created. (C) 2000 Federation of European Biochemical Societies.