TY - JOUR
T1 - Origin of the S* excited state feature of carotenoids in light-harvesting complex 1 from purple photosynthetic bacteria
AU - Niedzwiedzki, Dariusz M.
AU - Swainsbury, David J.K.
AU - Martin, Elizabeth C.
AU - Hunter, C. Neil
AU - Blankenship, Robert E.
N1 - Funding Information:
Spectroscopic studies were supported by the Photosynthetic Antenna Research Center, an Energy Frontier Research Center funded by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, under Award Number DE-SC 0001035. D.J.K.S., E.C.M., and C.N.H. were supported by a grant from the Biotechnology and Biological Sciences Research Council, UK (BB/M000265/1). C.N.H. acknowledges support from the European Research Council (Advanced Award 338895).
Publisher Copyright:
© 2017 American Chemical Society.
PY - 2017/8/17
Y1 - 2017/8/17
N2 - This spectroscopic study investigates the origin of the transient feature of the S* excited state of carotenoids bound in LH1 complexes from purple bacteria. The studies were performed on two RC-LH1 complexes from Rba. sphaeroides strains that bound carotenoids with different carbon−carbon double bond conjugation N, neurosporene (N = 9) and spirilloxanthin (N = 13). The S* transient spectral feature, originally associated with an elusive and optically silent excited state of spirilloxanthin in the LH1 complex, may be successfully explained and mimicked without involving any unknown electronic state. The spectral and temporal characteristics of the S* feature suggest that it is associated with triplet−triplet annihilation of carotenoid triplets formed after direct excitation of the molecule via a singlet fission mechanism. Depending on pigment homogeneity and carotenoid assembly in the LH1 complex, the spectro-temporal component associated with triplet−triplet annihilation may simply resolve a pure T-S spectrum of a carotenoid. In some cases (like spirilloxanthin), the T-S feature will also be accompanied by a carotenoid Stark spectrum and/or residual transient absorption of minor carotenoid species bound into LH1 antenna complex.
AB - This spectroscopic study investigates the origin of the transient feature of the S* excited state of carotenoids bound in LH1 complexes from purple bacteria. The studies were performed on two RC-LH1 complexes from Rba. sphaeroides strains that bound carotenoids with different carbon−carbon double bond conjugation N, neurosporene (N = 9) and spirilloxanthin (N = 13). The S* transient spectral feature, originally associated with an elusive and optically silent excited state of spirilloxanthin in the LH1 complex, may be successfully explained and mimicked without involving any unknown electronic state. The spectral and temporal characteristics of the S* feature suggest that it is associated with triplet−triplet annihilation of carotenoid triplets formed after direct excitation of the molecule via a singlet fission mechanism. Depending on pigment homogeneity and carotenoid assembly in the LH1 complex, the spectro-temporal component associated with triplet−triplet annihilation may simply resolve a pure T-S spectrum of a carotenoid. In some cases (like spirilloxanthin), the T-S feature will also be accompanied by a carotenoid Stark spectrum and/or residual transient absorption of minor carotenoid species bound into LH1 antenna complex.
UR - http://www.scopus.com/inward/record.url?scp=85030750186&partnerID=8YFLogxK
U2 - 10.1021/acs.jpcb.7b04251
DO - 10.1021/acs.jpcb.7b04251
M3 - Article
C2 - 28719215
AN - SCOPUS:85030750186
VL - 121
SP - 7571
EP - 7585
JO - Journal of Physical Chemistry B
JF - Journal of Physical Chemistry B
SN - 1520-6106
IS - 32
ER -