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PHOTOBIOPHYSICS |
1 Institute of Chemistry, Chinese Academy of Sciences
2 Institute of Botany, Chinese Academy of Sciences
* To whom correspondence should be addressed. E-mail: jpzhang{at}mail.iccas.ac.cn.
Submitted on October 25, 2005
Revised on December 6, 2005
Accepted on 3 March 2006
| Abstract |
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-carotene free in n-hexane, the lifetimes of the two low-lying singlet excited states, S1(2Ag-) and S2(1Bu+), are determined to be 14.3 ± 0.4 ps and 230 ± 10 fs, respectively. For the Cyt b6f complex, to which 9-cis-
-carotene is bounded, the lifetime of S1(2Ag-) state remains unchanged, while that of the S2(1Bu+) state is significantly reduced. In addition, a decay-to-rise correlation between the excited state dynamics of
-carotene and Chl a is clearly observed. These spectroscopic evidence prove that the S2(1Bu+) state is able to transfer electronic excitations to the Qx state of Chl a, whereas the S1(2Ag-) state remains inactive. The time constant and the partial efficiency of the energy transfer are determined to be 240 ± 40 fs and (49 ± 4)%, respectively, which supports the overall efficiency of 24% determined with steady state fluorescence spectroscopy. A scheme of the
-carotene-to-Chl a singlet energy transfer is proposed based on the excited-state dynamics of the pigments.
Key Words: Bryopsis corticulans, Cytochrome b6f complex, alpha-carotene, chlorophyll, energy transfer, time-resolved spectroscopy
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