ENERGETICS AND MECHANISM OF PRIMARY CHARGE SEPARATION IN BACTERIAL PHOTOSYNTHESIS - A COMPARATIVE-STUDY ON REACTION CENTERS OF RHODOBACTER-SPHAEROIDES AND CHLOROFLEXUS-AURANTIACUS
M. Volk et al., ENERGETICS AND MECHANISM OF PRIMARY CHARGE SEPARATION IN BACTERIAL PHOTOSYNTHESIS - A COMPARATIVE-STUDY ON REACTION CENTERS OF RHODOBACTER-SPHAEROIDES AND CHLOROFLEXUS-AURANTIACUS, JOURNAL OF PHYSICAL CHEMISTRY B, 102(4), 1998, pp. 735-751
The high efficiency of charge separation in photosynthetic reaction ce
nters arises from the interplay of energetics, electronic couplings, a
nd reorganization energies relevant for the fast charge separation and
slow recombination processes. All these parameters can be determined
unambiguously only from magnetic-field-dependent measurements of the r
ecombination dynamics of the intermediate radical pair P+HA- and the l
ifetime of the recombination product P-3. Results Obtained on Q(A)-de
pleted reaction centers of Chloroflexus aurantiacus are compared with
those for the well-characterized reaction centers of Rhodobacter sphae
roides. In contrast to Rb. sphaeroides, the magnetic field dependence
of the triplet yield in Cf. aurantiacus has a pronounced resonance str
ucture, allowing the direct determination of the exchange interaction
of P+HA-, J = 21 G. The recombination rate k(T) is slightly larger for
Cf. aurantiacus and shows a different temperature dependence. All the
se differences can be explained by the free energy of P+HA-, found to
be larger by 0.04 eV in Cf. aurantiacus compared to Rb. sphaeroides. W
e propose that this different energy arises largely from the different
amino acid at position L104, which is glutamic acid in the case of Rb
. sphaeroides and glutamine in the case of Cf. aurantiacus. The electr
onic couplings and the reorganization energies, on the other hand, are
very similar in both reaction centers. Implications for the mechanism
of primary charge separation are discussed. The pronounced nonexponen
tial kinetics of charge separation in Cf. aurantiacus is explained by
the energetic inhomogeneity of the primary radical pair P+BA-.