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Role of the reversible xanthophyll cycle in the photosystem II damage and repair cycle in Dunaliella salina

机译:叶黄素可逆循环在盐生杜氏盐藻光系统II损伤和修复循环中的作用

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摘要

The Dunaliella salina photosynthetic apparatus organization and function was investigated in wild type (WT) and a mutant (zea1) lacking all beta,beta-epoxycarotenoids derived from zeaxanthin (Z). The zeal mutant lacked antheraxanthin, violaxanthin, and neoxanthin from its thylakoid membranes but constitutively accumulated Z instead. It also lacked the so-called xanthophyll cycle, which, upon irradiance stress, reversibly converts violaxanthin to Z via a de-epoxidation reaction. Despite the pronounced difference observed in the composition of beta,beta-epoxycarotenoids between WT and zea1, no discernible difference could be observed between the two strains in terms of growth, photosynthesis, organization of the photosynthetic apparatus, photo-acclimation, sensitivity to photodamage, or recovery from photo-inhibition. WT and zeal were probed for the above parameters over a broad range of growth irradiance and upon light shift experiments (low light to high light shift and vice versa). A constitutive accumulation of Z in the zeal strain did not affect the acclimation of the photosynthetic apparatus to irradiance, as evidenced by indistinguishable irradiance-dependent adjustments in the chlorophyll antenna size and photosystem content of WT and zeal strain. In addition, a constitutive accumulation of Z in the zeal strain did not affect rates of photodamage or the recovery of the photosynthetic apparatus from photo-inhibition. However, Z in the WT accumulated in parallel with the accumulation of photodamaged PSII centers in the chloroplast thylakoids and decayed in tandem with a chloroplast recovery from photo-inhibition. These results suggest a role for Z in the protection of photodamaged and disassembled PSII reaction centers, apparently needed while PSII is in the process of degradation and replacement of the D1/32-kD reaction center protein.
机译:在野生型(WT)和突变体(zea1)中研究了杜氏盐藻光合装置的组织和功能,该突变体缺乏所有来自玉米黄质(Z)的β,β-环氧类胡萝卜素。热情的突变体的类囊体膜缺乏花药黄素,紫黄质和新黄质,但组成性地积累了Z。它还缺乏所谓的叶黄素循环,在辐照胁迫下,叶黄素循环通过脱环氧化反应可逆地将紫黄质转化为Z。尽管在WT和zea1之间观察到β,β-环氧类胡萝卜素的组成存在明显差异,但在生长,光合作用,光合装置的组织,光适应,对光损伤的敏感性,或从光抑制中恢复。在较宽的生长辐照度范围内以及在光移实验(低光到高光移,反之亦然)上探测了WT和热忱的上述参数。 Z在热忱菌株中的本构积累不会影响光合设备对辐照度的适应性,这是由WT与热忱菌株的叶绿素天线尺寸和光系统含量的不可区别的辐照度依赖性调整所证明的。另外,Z在热忱菌株中的本构积累不影响光损伤的速率或光合装置从光抑制中的恢复。但是,WT中的Z与叶绿体类囊体中光损伤的PSII中心的积累平行积累,并随着光抑制的恢复而与叶绿体串联。这些结果表明Z在保护光损坏和分解的PSII反应中心中发挥了作用,而在PSII降解和替换D1 / 32-kD反应中心蛋白的过程中显然需要Z。

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