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Reconstitution of photosynthetic charge accumulation and oxygen evolution in CaCl2‐treated PS II particles

机译:CaCl2处理的PS II颗粒中光合电荷积累和氧释放的重构

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>Extraction of PS II particles with 1 M CaCl2 caused complete disappearance of the light-induced signal of the possible Kok S2 state of the water-splitting complex and total loss of the O2, evolving activity, concomitant with perfect removal of the 17-, 23- and 34-kDa proteins from the particles. The recovery of the multiline signal in the CaCl2-treated PS II was performed by reinserting the 34-kDa protein, when CI− was present in the solution for the EPR measurement. However, in the absence of Cl−, besides the 34-kDa protein, the 17- and 23-kDa proteins were required for the recovery of the signal. These results are compared with the results on the recovery of the O2, evolution in the reconstituted PS II to examine the role of these three proteins on the water splitting.
机译:>用1 M CaCl 2 提取PS II颗粒导致水分解复合物的可能的Kok S 2 状态的光诱导信号完全消失,并且O 2 的总损失,不断发展的活性,以及​​从颗粒中完全去除17-,23-和34-kDa蛋白的过程。当溶液中存在CI -进行EPR测量时,通过重新插入34-kDa蛋白,在CaCl 2 处理的PS II中恢复多线信号。 。但是,在不存在Cl -的情况下,除了34-kDa蛋白外,还需要17-和23-kDa蛋白来恢复信号。将这些结果与O 2 的回收率,重组PS II中的进化结果进行比较,以检验这三种蛋白质在水分解中的作用。

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