Polívka Tomas, Niedzwiedzki Dariusz, Fuciman Marcel, Sundström Villy, Frank Harry A
Institute of Physical Biology, University of South Bohemia, Nove Hrady, Czech Republic.
J Phys Chem B. 2007 Jun 28;111(25):7422-31. doi: 10.1021/jp071395c. Epub 2007 Jun 5.
The role of the B800 in energy and electron transfer in LH2 complexes has been studied using femtosecond time-resolved transient absorption spectroscopy. The B800 site was perturbed by application of lithium dodecyl sulfate (LDS), and comparison of treated and untreated LH2 complexes from Rhodobacter sphaeroides incorporating carotenoids neurosporene, spheroidene, and spheroidenone was used to explore the role of B800 in carotenoid to bacteriochlorophyll-a (BChla) energy transfer and carotenoid radical formation. Efficiencies of the S1-mediated energy transfer in the LDS-treated complexes were 86, 61, and 57% in the LH2 complexes containing neurosporene, spheroidene, and spheroidenone, respectively. Analysis of the carotenoid S1 lifetimes in solution, LDS-treated, and untreated LH2 complexes allowed determination of B800/B850 branching ratio in the S1-mediated energy transfer. It is shown that B800 is a major acceptor, as approximately 60% of the energy from the carotenoid S1 state is accepted by B800. This value is nearly independent of conjugation length of the carotenoid. In addition to its role in energy transfer, the B800 BChla is the only electron acceptor in the event of charge separation between carotenoid and BChla in LH2 complexes, which is demonstrated by prevention of carotenoid radical formation in the LDS-treated LH2 complexes. In the untreated complexes containing neurosporene and spheroidene, the carotenoid radical is formed with a time constant of 300-400 fs. Application of different excitation wavelengths and intensity dependence of the carotenoid radical formation showed that the carotenoid radical can be formed only after excitation of the S2 state of carotenoid, although the S2 state itself is not a precursor of the charge-separated state. Instead, either a hot S1 state or a charge-transfer state lying between S2 and S1 states of the carotenoid are discussed as potential precursors of the charge-separated state.
利用飞秒时间分辨瞬态吸收光谱研究了B800在LH2复合物能量和电子转移中的作用。通过应用十二烷基硫酸锂(LDS)对B800位点进行扰动,并比较来自球形红细菌的含有类胡萝卜素神经孢烯、球形烯和球形异戊二烯酮的经处理和未处理的LH2复合物,以探究B800在类胡萝卜素向细菌叶绿素a(BChla)能量转移和类胡萝卜素自由基形成中的作用。在含有神经孢烯、球形烯和球形异戊二烯酮的LH2复合物中,LDS处理的复合物中S1介导的能量转移效率分别为86%、61%和57%。分析类胡萝卜素在溶液中、LDS处理的和未处理的LH2复合物中的S1寿命,可确定S1介导的能量转移中B800/B850分支比。结果表明,B800是主要受体,因为来自类胡萝卜素S1态的约60%的能量被B800接受。该值几乎与类胡萝卜素的共轭长度无关。除了在能量转移中的作用外,B800 BChla是LH2复合物中类胡萝卜素和BChla之间发生电荷分离时唯一的电子受体,这通过LDS处理的LH2复合物中类胡萝卜素自由基形成的抑制得以证明。在含有神经孢烯和球形烯的未处理复合物中,类胡萝卜素自由基以300 - 400飞秒的时间常数形成。不同激发波长的应用以及类胡萝卜素自由基形成的强度依赖性表明,类胡萝卜素自由基只能在类胡萝卜素S2态激发后形成,尽管S2态本身不是电荷分离态的前体。相反,类胡萝卜素的热S1态或位于S2和S1态之间的电荷转移态被讨论为电荷分离态的潜在前体。