A. N. Belozersky Institute of Physical-Chemical Biology, Moscow State University, 119991 Moscow, Russia.
Biochemistry (Mosc). 2012 Sep;77(9):1011-20. doi: 10.1134/S0006297912090088.
Time-resolved differential spectra of photosystem I complex were obtained by the "pump-probe" technique with 25-fs pulses with maxima at 670, 700, and 720 nm. The ratio between the number of excited chlorophyll molecules of the antenna and of the reaction center was shown to depend on spectral characteristics of the pump pulses. In all cases, an ultrafast (<150 fs) formation of the primary radical pair P700(+)A(0)() was recorded. However, on excitation by pulses with maxima at 670 or 700 nm, detection of the charge separation was masked by the much more intensive bleaching at the chlorophyll Q(y) band due to excitation of the bulk antenna chlorophylls. We show that triggering the charge separation by 25-fs pulses centered at 720 nm allows to detect more clearly kinetics of formation of the primary and secondary ion-radical pairs. The findings help to explain possible reasons for discrepancies of kinetics of primary steps of electron transfer detected in different laboratories.
利用 670、700 和 720nm 波长的 25fs 脉冲“泵浦-探测”技术获得了光系统 I 复合物的时间分辨差谱。结果表明,天线和反应中心激发态叶绿素分子数的比值取决于泵浦脉冲的光谱特性。在所有情况下,均记录到了超快(<150fs)的 P700(+)A(0)() 初级自由基对的形成。然而,当用 670nm 或 700nm 波长的脉冲激发时,由于激发体相天线叶绿素,在叶绿素 Q(y) 带处的漂白强度更大,掩盖了电荷分离的检测。我们表明,通过以 720nm 为中心的 25fs 脉冲触发电荷分离,可以更清楚地检测到初级和次级离子自由基对形成的动力学。这些发现有助于解释不同实验室检测到的电子转移初级步骤动力学存在差异的可能原因。