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The Stromal Chloroplast Deg7 Protease Participates in the Repair of Photosystem II after Photoinhibition in Arabidopsis1[W][OA]

机译:拟南芥中光抑制后基质金属叶绿体Deg7蛋白酶参与光系统II的修复[W] [OA]

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摘要

Light is the ultimate source of energy for photosynthesis; however, excessive light leads to photooxidative damage and hence reduced photosynthetic efficiency, especially when combined with other abiotic stresses. Although the photosystem II (PSII) reaction center D1 protein is the primary target of photooxidative damage, other PSII core proteins are also damaged and degraded. However, it is still largely unknown whether degradation of D1 and other PSII proteins involves previously uncharacterized proteases. Here, we show that Deg7 is peripherally associated with the stromal side of the thylakoid membranes and that Deg7 interacts directly with PSII. Our results show that Deg7 is involved in the primary cleavage of photodamaged D1, D2, CP47, and CP43 and that this activity is essential for its function in PSII repair. The double mutants deg5 deg7 and deg8 deg7 showed no obvious phenotypic differences under normal growth conditions, but additive effects were observed under high light. These results suggest that Deg proteases on both the stromal and luminal sides of the thylakoid membranes are important for the efficient PSII repair in Arabidopsis (Arabidopsis thaliana).
机译:光是光合作用的最终能源。但是,过多的光会导致光氧化损伤,从而降低光合效率,尤其是在与其他非生物胁迫结合使用时。尽管光系统II(PSII)反应中心D1蛋白是光氧化损伤的主要目标,但其他PSII核心蛋白也被破坏和降解。但是,D1和其他PSII蛋白的降解是否涉及以前未表征的蛋白酶仍是很大程度上未知的。在这里,我们显示Deg7在周围与类囊体膜的基质侧相关,并且Deg7与PSII直接相互作用。我们的结果表明,Deg7与光损伤的D1,D2,CP47和CP43的初级切割有关,并且该活性对其在PSII修复中的功能至关重要。在正常生长条件下,双突变体deg5 deg7和deg8 deg7没有明显的表型差异,但在强光下观察到累加效应。这些结果表明类囊体膜的基质和腔侧的Deg蛋白酶对于拟南芥(Arabidopsis thaliana)中有效的PSII修复很重要。

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