Rappaport Fabrice, Cuni Aude, Xiong Ling, Sayre Richard, Lavergne Jérôme
Institut de Biologie Physico-Chimique, Centre National de la Recherche Scientifique UPR 1261, Paris, France.
Biophys J. 2005 Mar;88(3):1948-58. doi: 10.1529/biophysj.104.050237. Epub 2005 Jan 14.
In the recombination process of Photosystem II (S(2)Q(A)(-)-->S(1)Q(A)) the limiting step is the electron transfer from the reduced primary acceptor pheophytin Ph(-) to the oxidized primary donor P(+) and the rate depends on the equilibrium constant between states S(2)PPhQ(A)(-) and S(1)P(+)Ph(-)Q(A). Accordingly, mutations that affect the midpoint potential of Ph or of P result in a modified recombination rate. A strong correlation is observed between the effects on the recombination rate and on thermoluminescence (TL, the light emission from S(2)Q(A)(-) during a warming ramp): a slower recombination corresponds to a large enhancement and higher temperature of the TL peak. The current theory of TL does not account for these effects, because it is based on the assumption that the rate-limiting step coincides with the radiative process. When implementing the known fact that the radiative pathway represents a minor leak, the modified TL theory readily accounts qualitatively for the observed behavior. However, the peak temperature is still lower than predicted from the temperature-dependence of recombination. We argue that this reflects the heterogeneity of the recombination process combined with the enhanced sensitivity of TL to slower components. The recombination kinetics are accurately fitted as a sum of two exponentials and we show that this is not due to a progressive stabilization of the charge-separated state, but to a pre-existing conformational heterogeneity.
在光系统II的重组过程(S(2)Q(A)(-) --> S(1)Q(A))中,限速步骤是电子从还原的初级受体脱镁叶绿素Ph(-)转移到氧化的初级供体P(+),其速率取决于状态S(2)PPhQ(A)(-)和S(1)P(+)Ph(-)Q(A)之间的平衡常数。因此,影响Ph或P中点电位的突变会导致重组速率发生改变。在对重组速率的影响和对热释光(TL,升温过程中S(2)Q(A)(-)的发光)的影响之间观察到强烈的相关性:较慢的重组对应于TL峰的大幅增强和更高温度。当前的TL理论无法解释这些影响,因为它基于限速步骤与辐射过程一致的假设。当考虑到辐射途径是一个小泄漏这一已知事实时,改进后的TL理论很容易定性地解释观察到的行为。然而,峰值温度仍然低于根据重组的温度依赖性预测的值。我们认为这反映了重组过程的异质性以及TL对较慢组分的增强敏感性。重组动力学可以精确地拟合为两个指数之和,我们表明这不是由于电荷分离态的逐渐稳定,而是由于预先存在的构象异质性。