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首页> 外文期刊>Frontiers in Plant Science >Chloroplast ATP Synthase Modulation of the Thylakoid Proton Motive Force: Implications for Photosystem I and Photosystem II Photoprotection
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Chloroplast ATP Synthase Modulation of the Thylakoid Proton Motive Force: Implications for Photosystem I and Photosystem II Photoprotection

机译:类囊体质子动力的叶绿体ATP合酶调节:对光系统I和光系统II光保护的影响。

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In wild type plants, decreasing CO_(2)lowers the activity of the chloroplast ATP synthase, slowing proton efflux from the thylakoid lumen resulting in buildup of thylakoid proton motive force ( pmf ). The resulting acidification of the lumen regulates both light harvesting, via the q_(E)mechanism, and photosynthetic electron transfer through the cytochrome b_(6)f complex. Here, we show that the cfq mutant of Arabidopsis, harboring single point mutation in its γ-subunit of the chloroplast ATP synthase, increases the specific activity of the ATP synthase and disables its down-regulation under low CO_(2). The increased thylakoid proton conductivity (g_(H)~(+)) in cfq results in decreased pmf and lumen acidification, preventing full activation of q_(E)and more rapid electron transfer through the b_(6)f complex, particularly under low CO_(2)and fluctuating light. These conditions favor the accumulation of electrons on the acceptor side of PSI, and result in severe loss of PSI activity. Comparing the current results with previous work on the pgr5 mutant suggests a general mechanism where increased PSI photodamage in both mutants is caused by loss of pmf , rather than inhibition of CEF per se . Overall, our results support a critical role for ATP synthase regulation in maintaining photosynthetic control of electron transfer to prevent photodamage.
机译:在野生型植物中,降低CO_(2)会降低叶绿体ATP合酶的活性,减慢类囊体腔的质子流出,从而导致类囊体质子动力(pmf)的积累。管腔的酸化调节通过q_(E)机理的光收集和通过细胞色素b_(6)f络合物的光合电子转移。在这里,我们显示拟南芥的cfq突变体,在其叶绿体ATP合酶的γ亚基中具有单点突变,增加了ATP合酶的比活性,并在低CO_(2)下禁用了其下调。 cfq中类囊体质子电导率(g_(H)〜(+))的增加导致pmf降低和管腔酸化,从而阻止q_(E)的完全活化以及通过b_(6)f配合物的更快电子转移,特别是在低电子发射率下CO_(2)和波动的光。这些条件有利于电子在PSI受体侧的积累,并导致PSI活性严重丧失。将目前的结果与对pgr5突变体的先前工作进行比较,提出了一种普遍的机制,其中两个突变体中PSI光损伤的增加是由pmf的损失引起的,而不是CEF本身的抑制。总体而言,我们的结果支持ATP合酶调节在维持光合作用控制电子传递以防止光损伤方面的关键作用。

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