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Title: Nonphotochemical hole burning of the reaction center of Rhodopseudomonas viridis

Journal Article · · Journal of Physical Chemistry; (United States)
DOI:https://doi.org/10.1021/j100128a031· OSTI ID:5136106
; ;  [1]
  1. Iowa State Univ., Ames, IA (United States)

Reddy et al. (Science, accepted) have reported persistent, nonphotochemical hole-burned (NPHB) spectra for the Q[sub y] states of the reaction center of Rhodopseudomonas viridis. The photoinduced structural transformation was shown to be highly localized on the special pair. This transformation leads to a red shift of the special pair's lowest-energy absorption band, P960, of 150 cm[sup [minus]1] and a comparable blue shift for a state at 850 nm, which, as a consequence, could be assigned as being most closely associated with the upper dimer component. Additional experimental results are presented here together with a theoretical analysis of the extent to which the NPHB spectra provide information on the contribution from the bacteriochlorophyll monomers of the special pair to the Q[sub y] states that absorb higher in energy than P960. Structured photochemical hole-burned (PHB) spectra of P960 are also presented that underscore the importance of strong electron-phonon coupling from a broad distribution of modes with a mean frequency of 30 cm[sup [minus]1] for an understanding of the P960 absorption profile. These spectra also identify the zero-phonon hole of the strongly damped special pair marker mode (145 cm[sup [minus]1]) and its associated phonon sideband structure. Calculated spectra are presented which are in good agreement with the experimental PHB spectra. 30 refs., 6 figs., 4 tabs.

DOE Contract Number:
W-7405-ENG-82
OSTI ID:
5136106
Journal Information:
Journal of Physical Chemistry; (United States), Vol. 97:26; ISSN 0022-3654
Country of Publication:
United States
Language:
English