Division of Material Science, Graduate School of Science, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8602, Japan.
Division of Material Science, Graduate School of Science, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8602, Japan.
Biochim Biophys Acta Bioenerg. 2018 Feb;1859(2):129-136. doi: 10.1016/j.bbabio.2017.11.004. Epub 2017 Nov 22.
Light-induced Fourier transformed infrared (FTIR) difference spectroscopy is a powerful method to study the structures and reactions of redox cofactors involved in the photosynthetic electron transport chain. So far, most of the FTIR studies of the reactions of oxygenic photosynthesis have been performed using isolated photosystem I (PSI) and photosystem II (PSII) preparations, which, however, could be modified during isolation procedures. In this study, we developed a methodology to evaluate the photosynthetic activities of thylakoids using FTIR spectroscopy. FTIR difference spectra upon successive flashes using thylakoids from spinach exhibited signals typical of the S-state cycle at the MnCaO cluster and Q reactions in PSII with period-four and -two oscillations, respectively. Similar measurement in the presence of an artificial quinone as an exogenous electron acceptor showed features specific to the S-state cycle. Simulations of the oscillation patterns provided the quantum efficiencies of the S-state cycle and electron transfer in PSII. Moreover, FTIR measurement under continuous illumination on thylakoids in the presence of DCMU showed signals due to Q reduction and P700 oxidation simultaneously. From the relative amplitudes of marker bands of Q and P700, the molar ratio of photoactive PSII and PSI centers in thylakoids was estimated. FTIR analyses of the photo-reactions in thylakoids, which are more intact than isolated photosystems, will be useful in investigations of the photosynthetic mechanism especially by genetic modification of photosystem proteins.
光诱导傅里叶变换红外(FTIR)差谱法是研究光合作用电子传递链中氧化还原辅助因子结构和反应的有力方法。到目前为止,大多数关于放氧光合作用反应的 FTIR 研究都是使用分离的光系统 I(PSI)和光系统 II(PSII)制剂进行的,然而,这些制剂在分离过程中可能会发生修饰。在这项研究中,我们开发了一种使用 FTIR 光谱评估类囊体光合作用活性的方法。使用菠菜类囊体进行连续闪光的 FTIR 差谱显示 MnCaO 簇处 S 态循环的信号以及 PSII 中的 Q 反应具有典型的四周期和二周期振荡。在存在人工醌作为外源电子受体的情况下进行类似的测量显示出 S 态循环的特征信号。振荡模式的模拟提供了 PSII 中 S 态循环和电子传递的量子效率。此外,在 DCMU 存在下连续光照下对类囊体进行 FTIR 测量时,同时显示出 Q 还原和 P700 氧化的信号。从 Q 和 P700 的标记带的相对幅度,可以估计类囊体中光活性 PSII 和 PSI 中心的摩尔比。与分离的光合系统相比,类囊体中光反应的 FTIR 分析更完整,这将有助于研究光合作用机制,特别是通过对光合系统蛋白进行遗传修饰。