ENERGY-TRANSFER IN SPECTRALLY INHOMOGENEOUS LIGHT-HARVESTING PIGMENT-PROTEIN COMPLEXES OF PURPLE BACTERIA

Citation
S. Hess et al., ENERGY-TRANSFER IN SPECTRALLY INHOMOGENEOUS LIGHT-HARVESTING PIGMENT-PROTEIN COMPLEXES OF PURPLE BACTERIA, Biophysical journal, 69(6), 1995, pp. 2211-2225
Citations number
56
Categorie Soggetti
Biophysics
Journal title
ISSN journal
00063495
Volume
69
Issue
6
Year of publication
1995
Pages
2211 - 2225
Database
ISI
SICI code
0006-3495(1995)69:6<2211:EISILP>2.0.ZU;2-Z
Abstract
Energy transfer within the peripheral light-harvesting antenna of the purple bacteria Rhodobacter sphaeroides and Rhodopseudomonas palustris was studied by one- and two-color pump-probe absorption spectroscopy with similar to 100-fs tunable pulses at room temperature and at 77 K. The energy transfer from B800 to B850 occurs with a time constant of 0.7 +/- 0.05 ps at room temperature and 1.8 +/- 0.2 ps at 77 K and is similar in both species. Anisotropy measurements suggest a limited but fast B800 <----> B800 transfer time (tau similar to 0.3 ps). This is analyzed as incoherent hopping of the excitation in a system of spectr ally inhomogeneous antenna pigment-protein complexes, by a master equa tion approach, The simulations show that the measured B800 dynamics is well described as energy transfer with a characteristic average neare st-neighbor pairwise transfer time of 0.35 ps among similar to 10 Bchl molecules in a circular arrangement, in good agreement with the recen t high-resolution structure of LH2, The possible presence of fast intr amolecular relaxation processes within the Bchl a molecule was investi gated by measurement of time-resolved difference absorption spectra an d kinetics of Bchl a in solution and in low-temperature glasses, From these measurements it is concluded that fast transients observed at ro om temperature are due mainly to solvation processes, whereas at 77 K predominantly slower (>10-ps) relaxation occurs.