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Using site-directed mutagenesis to probe the role of the D2 carotenoid in the secondary electron-transfer pathway of photosystem II

机译:使用定点诱变来探究D2类胡萝卜素在光系统II的二次电子传递途径中的作用

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摘要

Secondary electron transfer in photosystem II (PSII), which occurs when water oxidation is inhibited, involves redox-active carotenoids (Car), as well as chlorophylls (Chl), and cytochrome b559 (Cyt b559), and is believed to play a role in photoprotection. CarD2 may be the initial point of secondary electron transfer because it is the closest cofactor to both P680, the initial oxidant, and to Cyt b559, the terminal secondary electron donor within PSII. In order to characterize the role of CarD2 and to determine the effects of perturbing CarD2 on both the electron-transfer events and on the identity of the redox-active cofactors, it is necessary to vary the properties of CarD2 selectively without affecting the ten other Car per PSII. To this end, site-directed mutations around the binding pocket of CarD2 (D2-G47W, D2-G47F, and D2-T50F) have been generated in Synechocystis sp. PCC 6803. Characterization by near-IR and EPR spectroscopy provides the first experimental evidence that CarD2 is one of the redox-active carotenoids in PSII. There is a specific perturbation of the Car∙+ near-IR spectrum in all three mutated PSII samples, allowing the assignment of the spectral signature of CarD2∙+; CarD2∙+ exhibits a near-IR peak at 980 nm and is the predominant secondary donor oxidized in a charge separation at low temperature in ferricyanide-treated wild-type PSII. The yield of secondary donor radicals is substantially decreased in PSII complexes isolated from each mutant. In addition, the kinetics of radical formation are altered in the mutated PSII samples. These results are consistent with oxidation of CarD2 being the initial step in secondary electron transfer. Furthermore, normal light levels during mutant cell growth perturb the shape of the Chl∙+ near-IR absorption peak and generate a dark-stable radical observable in the EPR spectra, indicating a higher susceptibility to photodamage further linking the secondary electron-transfer pathway to photoprotection.Electronic supplementary materialThe online version of this article (doi:10.1007/s11120-013-9793-6) contains supplementary material, which is available to authorized users.
机译:当抑制水氧化时,发生在光系统II(PSII)中的二次电子转移,涉及氧化还原活性类胡萝卜素(Car),叶绿素(Chl)和细胞色素b559(Cyt b559),并且据认为起一定作用在光保护。 CarD2可能是二次电子转移的起始点,因为它是与初始氧化剂P680和PSII中末端二次电子供体Cyt b559最接近的辅助因子。为了表征CarD2的作用并确定扰动CarD2对电子转移事件和氧化还原活性辅因子的影响,有必要在不影响其他十种Car的情况下选择性地改变CarD2的特性。根据PSII。为此,在Synechocystis sp。中产生了CarD2结合口袋周围的定点突变(D2-G47W,D2-G47F和D2-T50F)。 PCC6803。通过近红外和EPR光谱进行表征提供了第一个实验证据,表明CarD2是PSII中的一种氧化还原活性类胡萝卜素。在所有三个突变的PSII样本中,Car ∙+ 的近红外光谱都有特定的扰动,从而允许分配CarD2 ∙+ 的光谱特征。 CarD2 ∙+ 在980 nm处显示一个近红外峰,是铁氰化物处理过的野生型PSII在低温下的电荷分离中主要被氧化的次级供体。从每个突变体分离的PSII复合物中,次级供体基团的产率大大降低。此外,在突变的PSII样品中,自由基形成的动力学发生了变化。这些结果与CarD2的氧化是二次电子转移的第一步相一致。此外,突变细胞生长过程中的正常光照水平会扰乱Chl ∙+ 近红外吸收峰的形状,并在EPR光谱中产生可观察到的暗稳定自由基,表明对光损伤的敏感性更高电子补充材料本文的在线版本(doi:10.1007 / s11120-013-9793-6)包含补充材料,授权用户可以使用。

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