Savikhin S, Xu W, Martinsson P, Chitnis P R, Struve W S
Ames Laboratory-U.S. Department of Energy, Iowa State University, Ames, Iowa 50011, USA.
Biochemistry. 2001 Aug 7;40(31):9282-90. doi: 10.1021/bi0104165.
The charge separation P700A(0) --> P700(+)A(0)(-) and the subsequent electron transfer from the primary to secondary electron acceptor have been studied by subtracting absorption difference profiles for cyanobacterial photosystem I (PS I) complexes with open and closed reaction centers. Samples were excited at 660 nm, which lies toward the blue edge of the core antenna absorption spectrum. The resulting PS I kinetics were analyzed in terms of the relevant P700, P700(+), A(0), and A(0)(-) absorption spectra. In our kinetic model, the radical pair P700(+)A(0)(-) forms with 1.3 ps rise kinetics after creation of electronically excited P700. The formation of A(1)(-) via electron transfer from A(0)(-) requires approximately 13 ps. The kinetics of the latter step are appreciably faster than previously estimated by other groups (20--50 ps).
通过减去具有开放和关闭反应中心的蓝藻光系统I(PS I)复合物的吸收差异谱,研究了电荷分离P700A(0) --> P700(+)A(0)(-)以及随后从初级电子受体到次级电子受体的电子转移。样品在660 nm处激发,该波长位于核心天线吸收光谱的蓝边附近。根据相关的P700、P700(+)、A(0)和A(0)(-)吸收光谱分析得到的PS I动力学。在我们的动力学模型中,在电子激发的P700产生后,自由基对P700(+)A(0)(-)以1.3 ps的上升动力学形成。通过从A(0)(-)进行电子转移形成A(1)(-)大约需要13 ps。后一步的动力学明显快于其他研究小组先前估计的(20 - 50 ps)。