AFRC Photosynthesis Research Group, Wolfson Laboratories, Department of Biochemistry, Imperial College of Science, Technology, and Medicine, London SW7 2AY, United Kingdom.
Plant Physiol. 1992 May;99(1):21-5. doi: 10.1104/pp.99.1.21.
When pea plants (Pisum sativum L. cv Feltham First) are subjected to freezing conditions (-18 degrees C) followed by a thaw to 18 degrees 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 CaCl(2), 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(+).
当豌豆植株(Pisum sativum L. cv Feltham First)受到冷冻条件(-18°C)的影响,随后解冻至 18°C 时,使用富含光合系统 II(PSII)的分离类囊体膜片段判断,水分解能力会受到显著抑制(通过光诱导的 2,6-二氯苯酚靛酚还原速率来判断)。冷冻-解冻诱导的水分解活性抑制与 PSII 的 17-和 23 千道尔顿外在蛋白的丧失以及 33 千道尔顿蛋白结合力的减弱有关。没有明显的结合锰损失。然而,添加 10 毫摩尔氯化钙允许这些修饰的 PSII 富集颗粒的水分解活性完全恢复。发现 PSII 的组织和功能能力的冷冻-解冻诱导变化使其对光抑制的敏感性增加,这与随附论文中提出的概念一致,即氧化损伤可能由于 P680(+)的寿命延长而在 PSII 反应中心内发生。