FEMTOSECOND DYNAMICS IN ISOLATED LH2 COMPLEXES OF VARIOUS SPECIES OF PURPLE BACTERIA

Citation
Jtm. Kennis et al., FEMTOSECOND DYNAMICS IN ISOLATED LH2 COMPLEXES OF VARIOUS SPECIES OF PURPLE BACTERIA, JOURNAL OF PHYSICAL CHEMISTRY B, 101(39), 1997, pp. 7827-7834
Citations number
28
Categorie Soggetti
Chemistry Physical
Journal title
JOURNAL OF PHYSICAL CHEMISTRY B
ISSN journal
15206106 → ACNP
Volume
101
Issue
39
Year of publication
1997
Pages
7827 - 7834
Database
ISI
SICI code
1089-5647(1997)101:39<7827:FDIILC>2.0.ZU;2-B
Abstract
Polarized and magic angle two-color femtosecond spectroscopy was used to study B800-850 antenna complexes of the photosynthetic purple bacte ria Rhodopseudomonas acidophila (Rps. acidophila), Rhodobacter sphaero ides (Rb, sphaeroides), and Chromatium tepidum (Chr. tepidum) and the B800-820 complex of Chromatium vinosum at room temperature. As was ear lier found for Chr. tepidum, in the B800-850 complexes of Rps. acidoph ila and Rb. sphaeroides the bleaching signal of B850 was found to be s everal times larger than that of B800, indicating strong exciton inter actions between the bacteriochlorophylls (BChls) in the B850 aggregate . Depolarization of the B850 excited state was found to occur within o ur time resolution of 80 fs. In all species, B800 to B850 or B820 tran sfer took place with a time constant of 0.7 to 0.9 ps. Depolarization studies indicated a transfer time of 1.5 ps between B800 molecules in Rps. acidophila. In Chr. tepidum, B800 depolarizes 2 to 4 times slower , dependent on the wavelength of excitation. Our results indicate that the double band structure of B800 of the latter organism is due to tw o separate pools of BChls, rather than dimeric exciton interaction. Up on excitation of the B800-820 complex of Chr. vinosum at 795 nm, the B 820 absorbance difference spectrum shifted with time to the red by 20 nm, indicating that B820 is spectrally very heterogeneous. A 2 ps down hill energy transfer process within the B820 band is assigned to energ y transfer between aggregated B800-820 complexes. Assuming that the B8 00-820 complex is similar to B800-850, we propose that the large spect ral heterogeneity of B820 does not occur within individual B800-820 co mplexes.