TY - JOUR
T1 - Temporal and spectral characterization of the photosynthetic reaction center from Heliobacterium modesticaldum
AU - Chauvet, Adrien
AU - Sarrou, Josephine
AU - Lin, Su
AU - Romberger, Steven P.
AU - Golbeck, John H.
AU - Savikhin, Sergei
AU - Redding, Kevin E.
N1 - Funding Information:
Acknowledgments This work was funded by the Division of Chemical Sciences, Geosciences, and Biosciences, Office of Basic Energy Sciences of the U.S. Department of Energy through Grant DE-FG02-98ER20314 MOD012 to K.E.R. and J.H.G and through Grant DE-FG02-09ER16084 to S.S.
PY - 2013/9
Y1 - 2013/9
N2 - A time-resolved spectroscopic study of the isolated photosynthetic reaction center (RC) from Heliobacterium modesticaldum reveals that thermal equilibration of light excitation among the antenna pigments followed by trapping of excitation and the formation of the charge-separated state P 800 +A0 - occurs within ~25 ps. This time scale is similar to that reported for plant and cyanobacterial photosystem I (PS I) complexes. Subsequent electron transfer from the primary electron acceptor A0 occurs with a lifetime of ~600 ps, suggesting that the RC of H. modesticaldum is functionally similar to that of Heliobacillus mobilis and Heliobacterium chlorum. The (A0 - - A0) and (P800 + - P800) absorption difference spectra imply that an 81-OH-Chl a F molecule serves as the primary electron acceptor and occupies the position analogous to ec3 (A0) in PS I, while a monomeric BChl g pigment occupies the position analogous to ec2 (accessory Chl). The presence of an intense photobleaching band at 790 nm in the (A0 - - A0) spectrum suggests that the excitonic coupling between the monomeric accessory BChl g and the 8 1-OH-Chl a F in the heliobacterial RC is significantly stronger than the excitonic coupling between the equivalent pigments in PS I.
AB - A time-resolved spectroscopic study of the isolated photosynthetic reaction center (RC) from Heliobacterium modesticaldum reveals that thermal equilibration of light excitation among the antenna pigments followed by trapping of excitation and the formation of the charge-separated state P 800 +A0 - occurs within ~25 ps. This time scale is similar to that reported for plant and cyanobacterial photosystem I (PS I) complexes. Subsequent electron transfer from the primary electron acceptor A0 occurs with a lifetime of ~600 ps, suggesting that the RC of H. modesticaldum is functionally similar to that of Heliobacillus mobilis and Heliobacterium chlorum. The (A0 - - A0) and (P800 + - P800) absorption difference spectra imply that an 81-OH-Chl a F molecule serves as the primary electron acceptor and occupies the position analogous to ec3 (A0) in PS I, while a monomeric BChl g pigment occupies the position analogous to ec2 (accessory Chl). The presence of an intense photobleaching band at 790 nm in the (A0 - - A0) spectrum suggests that the excitonic coupling between the monomeric accessory BChl g and the 8 1-OH-Chl a F in the heliobacterial RC is significantly stronger than the excitonic coupling between the equivalent pigments in PS I.
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U2 - 10.1007/s11120-013-9871-9
DO - 10.1007/s11120-013-9871-9
M3 - Article
C2 - 23812833
AN - SCOPUS:84879334097
SN - 0166-8595
VL - 116
SP - 1
EP - 9
JO - Photosynthesis research
JF - Photosynthesis research
IS - 1
ER -