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首页> 外文期刊>Plant, Cell & Environment >Deletion of FtsH11 protease has impact on chloroplast structure and function in Arabidopsis thaliana when grown under continuous light
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Deletion of FtsH11 protease has impact on chloroplast structure and function in Arabidopsis thaliana when grown under continuous light

机译:在连续光照下生长时,FtsH11蛋白酶的缺失对拟南芥叶绿体结构和功能的影响

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摘要

The membrane-integrated metalloprotease FtsH11 of Arabidopsis thaliana is proposed to be dual-targeted to mitochondria and chloroplasts. A bleached phenotype was observed in ftsh11 grown at long days or continuous light, pointing to disturbances in the chloroplast. Within the chloroplast, FtsH11 was found to be located exclusively in the envelope. Two chloroplast-located proteins of unknown function (Tic22-like protein and YGGT-A) showed significantly higher abundance in envelope membranes and intact chloroplasts of ftsh11 and therefore qualify as potential substrates for the FtsH11 protease. No proteomic changes were observed in the mitochondria of 6-week-old ftsh11 compared with wild type, and FtsH11 was not immunodetected in these organelles. The abundance of plastidic proteins, especially of photosynthetic proteins, was altered even during standard growth conditions in total leaves of ftsh11. At continuous light, the amount of photosystem I decreased relative to photosystem II, accompanied by a drastic change of the chloroplast morphology and a drop of non-photochemical quenching. FtsH11 is crucial for chloroplast structure and function during growth in prolonged photoperiod.
机译:拟南芥的膜整合金属蛋白酶FtsH11被提议双重靶向线粒体和叶绿体。在长时间或连续光照下生长的ftsh11中观察到漂白表型,表明叶绿体受到干扰。在叶绿体中,发现FtsH11仅位于包膜中。功能未知的两个叶绿体定位蛋白(Tic22样蛋白和YGGT-A)在ftsh11的包膜和完整叶绿体中显示出较高的丰度,因此可以作为FtsH11蛋白酶的潜在底物。与野生型相比,在6周龄的ftsh11的线粒体中未观察到蛋白质组学变化,并且在这些细胞器中未免疫检测到FtsH11。即使在ftsh11的总叶片中标准生长条件下,质体蛋白(尤其是光合蛋白)的丰度也发生了变化。在连续光下,光系统I的数量相对于光系统II减少,伴随着叶绿体形态的急剧变化和非光化学猝灭的下降。 FtsH11对于延长光周期生长期间叶绿体的结构和功能至关重要。

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