The specific aims of the proposed research are to characterize the structural, vibronic, and electronic properties of the photophysically active bacteriochlorophyll (BChl) and bacteriopheophytin (BPh) cofactors in bacterial photosynthetic reaction centers (RCs). Bacterial RCs were chosen for study because of this class of proteins represents a prototypical model system for investigating the factors which mediate charge separation across a biological membrane. The utility of bacterial RCs for examining this process is due to the fact that (1) high-resolution X-ray crystallographic data are available for RCs from several species and (2) genetic engineering techniques are well developed for certain of these species. These two criteria are not satisfied for any mammalian membrane-bound proteins involved in primary charge-separation and energy-transduction processes. The principal investigative tool for the studies is resonance Raman (RR) spectroscopy. The first major objective is to characterize the properties of the BChl/BPh cofactors in genetically modified RCs which exhibit novel electron-transfer properties. These studies will focus on a series of mutants of Rb, capsulatus wherein replacements have been made in amino acid residues which are in close proximity to the accessory BChl and BPh cofactors on the electron-transfer active L branch of the protein. The genetically modified RCs will include mutants in which electron transfer has been first documented to proceed down the normally inactive M branch of the protein. In all cases the RR studies will be conducted on RCs hose detailed electron-transfer kinetics have been elucidated via time-resolved optical experiments. The second major objective is to conduct RR studies on RCs aimed at determining the nature of the low-frequency vibrational modes of athe BChl/BPh cofactors which are strongly coupled to the lowest- energy optical transition(s). The principal target of these studies is the primary electron donor. The characterization of the low-frequency modes will proceed via acquisition and analysis of RR data from RCs labeled with 15N, 26Mg, and 15N/26Mg. The long-term objective of all the studies is to determine how the physical properties of the cofactors (structure, electron-density distribution, electron-phonon coupling) govern and/or reflect their functional characteristics (electron transfer and charge separation across the biological membrane).

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM039781-10
Application #
2734592
Study Section
Special Emphasis Panel (ZRG3-BBCA (01))
Project Start
1988-07-01
Project End
2000-06-30
Budget Start
1998-07-01
Budget End
1999-06-30
Support Year
10
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of California Riverside
Department
Chemistry
Type
Schools of Earth Sciences/Natur
DUNS #
City
Riverside
State
CA
Country
United States
Zip Code
92521
Czarnecki, Kazimierz; Chen, Lei; Diers, James R et al. (2006) Low-frequency resonance Raman studies of the H(M202)G cavity mutant of bacterial photosynthetic reaction centers. Photosynth Res 88:31-41
Pendon, Zeus D; Sullivan, James O; van der Hoef, Ineke et al. (2005) Stereoisomers of carotenoids: spectroscopic properties of locked and unlocked cis-isomers of spheroidene. Photosynth Res 86:5-24
Tracewell, Cara A; Cua, Agnes; Bocian, David F et al. (2005) Resonance Raman spectroscopy of carotenoids in Photosystem II core complexes. Photosynth Res 83:45-52
Chen, Lei; Kirmaier, Christine; Holten, Dewey et al. (2005) Resonance Raman characterization of Rhodobacter capsulatus reaction centers with lysine mutations near the accessory bacteriochlorophylls. Photosynth Res 83:35-43
Cua, Agnes; Vrettos, John S; de Paula, Julio C et al. (2003) Raman spectra and normal coordinate analyses of low-frequency vibrations of oxo-bridged manganese complexes. J Biol Inorg Chem 8:439-51
Tracewell, C A; Cua, A; Stewart, D H et al. (2001) Characterization of carotenoid and chlorophyll photooxidation in photosystem II. Biochemistry 40:193-203
Czarnecki, K; Cua, A; Kirmaier, C et al. (1999) Relationship between altered structure and photochemistry in mutant reaction centers in which bacteriochlorophyll replaces the photoactive bacteriopheophytin. Biospectroscopy 5:346-57
Stewart, D H; Cua, A; Chisholm, D A et al. (1998) Identification of histidine 118 in the D1 polypeptide of photosystem II as the axial ligand to chlorophyll Z. Biochemistry 37:10040-6
Cua, A; Kirmaier, C; Holten, D et al. (1998) Resonance raman characterization of reaction centers with an Asp residue near the photoactive bacteriopheophytin. Biochemistry 37:6394-401
Czarnecki, K; Schenck, C C; Bocian, D F (1997) Resonance Raman characterization of reaction centers in which bacteriochlorophyll replaces the photoactive bacteriopheophytin. Biochemistry 36:14697-704

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