ENERGETICS AND MECHANISM OF PRIMARY CHARGE SEPARATION IN BACTERIAL PHOTOSYNTHESIS - A COMPARATIVE-STUDY ON REACTION CENTERS OF RHODOBACTER-SPHAEROIDES AND CHLOROFLEXUS-AURANTIACUS

Citation
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
Citations number
129
Categorie Soggetti
Chemistry Physical
Journal title
JOURNAL OF PHYSICAL CHEMISTRY B
ISSN journal
15206106 → ACNP
Volume
102
Issue
4
Year of publication
1998
Pages
735 - 751
Database
ISI
SICI code
1089-5647(1998)102:4<735:EAMOPC>2.0.ZU;2-5
Abstract
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-.