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Effect of Cold Treatments on the Binding Stability of Photosystem II Extrinsic Proteins and an Associated Increase in Susceptibility to Photoinhibition

机译:冷处理对光系统II外在蛋白的结合稳定性以及对光抑制敏感性的相关增加的影响

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摘要

When pea plants (Pisum sativum L. cv Feltham First) are subjected to freezing conditions (−18°C) followed by a thaw to 18°C, there is a significant inhibition of water-splitting capacity judged by the rate of light-induced reduction of 2,6-dichlorophenol indophenol using isolated thylakoid membrane fragments enriched in photosystem II (PSII). The freeze-thaw-induced inhibition of water-splitting activity has been correlated with the loss of the 17- and 23-kilodalton extrinsic protein of PSII and with a weakening of the binding of the 33-kilodalton protein. There was no apparent loss of bound manganese. Addition of 10 millimolar CaCl2, however, allowed a full recovery of the water-splitting activity of these modified PSII-enriched particles. The freeze-thaw-induced changes in the organization and functional capacity of PSII was found to increase its susceptibility to photoinhibition in agreement with the concepts presented in the accompanying paper, that oxidative damage can occur within the PSII reaction center as a consequence of extending the lifetime of P680+.
机译:当豌豆植物(Pisum sativum L. cv Feltham First)经受冷冻条件(−18°C),然后融化至18°C时,根据光诱导的速率判断,其对水分解能力的抑制作用显着。使用富集光系统II(PSII)的分离类囊体膜片段减少2,6-二氯苯酚吲哚酚的含量。冻融诱导的水分解活性的抑制与PSII的17和23千达尔顿外在蛋白的损失以及33千达尔顿蛋白的结合减弱有关。结合锰没有明显损失。然而,添加10毫摩尔的CaCl 2可以完全恢复这些改性的富含PSII的颗粒的水分解活性。发现冻融诱导的PSII的组织和功能能力变化会增加其对光抑制的敏感性,这与随附论文中提出的概念相一致,即由于PSII反应中心的扩展而可能发生氧化损伤。 P680 + 的使用寿命。

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