Sato Akihiko, Nakano Yuki, Nakamura Shin, Noguchi Takumi
Division of Material Science, Graduate School of Science, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8602, Japan.
J Phys Chem B. 2021 Apr 29;125(16):4031-4045. doi: 10.1021/acs.jpcb.1c01624. Epub 2021 Apr 16.
The catalytic center of photosynthetic water oxidation, the MnCaO cluster, is assembled in photosystem II (PSII) through a light-driven process called photoactivation, whose mechanism remains elusive. Here, we used rapid-scan time-resolved Fourier transform infrared (FTIR) spectroscopy combined with the attenuated total reflection (ATR) technique to monitor the photoactivation process. Rapid-scan ATR-FTIR spectra of apo-PSII with Mn upon flash illumination showed spectral features typical of carboxylate stretching vibrations, which were attributed to two carboxylate ligands, D1-D170 and D1-E189, by quantum chemical calculations. The FTIR signal decayed with a time constant of ∼0.7 s, showing that the subsequent "dark rearrangement" step occurred with a low quantum yield and Mn ions were mostly released during this decay. Simulation of the kinetic process provided a slow intrinsic rate of the dark rearrangement, which was attributed to a large protein conformational change. The photoassembly mechanism of the MnCaO cluster is proposed based on these findings.
光合水氧化的催化中心——锰钙氧簇(MnCaO),是通过一个称为光激活的光驱动过程在光系统II(PSII)中组装而成的,其机制仍然难以捉摸。在此,我们使用快速扫描时间分辨傅里叶变换红外(FTIR)光谱结合衰减全反射(ATR)技术来监测光激活过程。在闪光照射下,含有锰的脱辅基PSII的快速扫描ATR-FTIR光谱显示出羧酸盐伸缩振动的典型光谱特征,通过量子化学计算,这些特征归因于两个羧酸盐配体,即D1-D170和D1-E189。FTIR信号以约0.7秒的时间常数衰减,表明随后的“暗重排”步骤以低量子产率发生,并且在这种衰减过程中大部分锰离子被释放。动力学过程的模拟提供了暗重排的缓慢固有速率,这归因于大的蛋白质构象变化。基于这些发现,提出了MnCaO簇的光组装机制。