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甘氨酸甜菜碱减轻了高温下转基因番茄植株光系统 II 的光抑制。

Glycinebetaine mitigated the photoinhibition of photosystem II at high temperature in transgenic tomato plants.

机构信息

College of Life Science, State Key Laboratory of Crop Biology, Shandong Key Laboratory of Crop Biology, Shandong Agricultural University, Taian, China.

Department of Plant Physiology, Slovak University of Agriculture, Nitra, Slovakia.

出版信息

Photosynth Res. 2021 Mar;147(3):301-315. doi: 10.1007/s11120-020-00810-2. Epub 2021 Jan 4.

Abstract

Photosystem II (PSII), especially the D1 protein, is highly sensitive to the detrimental impact of heat stress. Photoinhibition always occurs when the rate of photodamage exceeds the rate of D1 protein repair. Here, genetically engineered codA-tomato with the capability to accumulate glycinebetaine (GB) was established. After photoinhibition treatment at high temperature, the transgenic lines displayed more thermotolerance to heat-induced photoinhibition than the control line. GB maintained high expression of LeFtsHs and LeDegs and degraded the damaged D1 protein in time. Meanwhile, the increased transcription of synthesis-related genes accelerated the de novo synthesis of D1 protein. Low ROS accumulation reduced the inhibition of D1 protein translation in the transgenic plants, thereby reducing protein damage. The increased D1 protein content and decreased phosphorylated D1 protein (pD1) in the transgenic plants compared with control plants imply that GB may minimize photodamage and maximize D1 protein stability. As D1 protein exhibits a high turnover, PSII maybe repaired rapidly and efficiently in transgenic plants under photoinhibition treatment at high temperature, with the resultant mitigation of photoinhibition of PSII.

摘要

光系统 II(PSII),尤其是 D1 蛋白,对热应激的有害影响高度敏感。当光损伤的速度超过 D1 蛋白修复的速度时,光抑制总会发生。在这里,建立了具有积累甜菜碱(GB)能力的基因工程 codA-番茄。在高温下进行光抑制处理后,与对照品系相比,转基因系对热诱导的光抑制表现出更高的耐热性。GB 保持 LeFtsHs 和 LeDegs 的高表达,并及时降解受损的 D1 蛋白。同时,合成相关基因的转录增加加速了 D1 蛋白的从头合成。ROS 积累减少降低了转基因植物中 D1 蛋白翻译的抑制,从而减少了蛋白损伤。与对照植物相比,转基因植物中 D1 蛋白含量增加和磷酸化 D1 蛋白(pD1)减少表明,GB 可能最大限度地减少光损伤并最大限度地提高 D1 蛋白稳定性。由于 D1 蛋白具有高周转率,在高温下进行光抑制处理时,PSII 可能在转基因植物中得到快速有效地修复,从而减轻 PSII 的光抑制。

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