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质体基质 Deg7 蛋白酶参与拟南芥光抑制后光系统 II 的修复。

The stromal chloroplast Deg7 protease participates in the repair of photosystem II after photoinhibition in Arabidopsis.

机构信息

Photosynthesis Research Center, Key Laboratory of Photobiology, Institute of Botany, Chinese Academy of Sciences, Beijing 100093, China.

出版信息

Plant Physiol. 2010 Mar;152(3):1263-73. doi: 10.1104/pp.109.150722. Epub 2010 Jan 20.

Abstract

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).

摘要

光是光合作用的最终能量来源;然而,过量的光会导致光氧化损伤,从而降低光合作用效率,尤其是与其他非生物胁迫相结合时。尽管光系统 II(PSII)反应中心 D1 蛋白是光氧化损伤的主要靶标,但其他 PSII 核心蛋白也会受到损伤和降解。然而,目前尚不清楚 D1 和其他 PSII 蛋白的降解是否涉及以前未表征的蛋白酶。在这里,我们表明 Deg7 与类囊体膜的基质侧外周相关联,并且 Deg7 与 PSII 直接相互作用。我们的结果表明 Deg7 参与光损伤的 D1、D2、CP47 和 CP43 的初步切割,并且该活性对于其在 PSII 修复中的功能是必需的。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,但在高光下观察到附加效应。这些结果表明,类囊体膜基质侧和腔侧上的 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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