Dynamic control of protein diffusion within the granal thylakoid lumen

被引:188
作者
Kirchhoff, Helmut [1 ]
Hall, Chris [1 ]
Wood, Magnus [1 ]
Herbstova, Miroslava [1 ]
Tsabari, Onie [2 ]
Nevo, Reinat [2 ]
Charuvi, Dana [2 ]
Shimoni, Eyal [3 ]
Reich, Ziv [2 ]
机构
[1] Washington State Univ, Inst Biol Chem, Pullman, WA 99164 USA
[2] Weizmann Inst Sci, Dept Biol Chem, IL-76100 Rehovot, Israel
[3] Weizmann Inst Sci, Electron Microscopy Unit, IL-76100 Rehovot, Israel
基金
以色列科学基金会;
关键词
PHOTOSYSTEM-II; HIGH-PRESSURE; SPINACH-CHLOROPLASTS; HIGHER-PLANT; PHOTOSYNTHETIC MEMBRANES; IN-VIVO; ORGANIZATION; COMPLEX; OXYGEN; PHOTOINHIBITION;
D O I
10.1073/pnas.1104141109
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The machinery that conducts the light-driven reactions of oxygenic photosynthesis is hosted within specialized paired membranes called thylakoids. In higher plants, the thylakoids are segregated into two morphological and functional domains called grana and stroma lamellae. A large fraction of the luminal volume of the granal thylakoids is occupied by the oxygen-evolving complex of photosystem II. Electron microscopy data we obtained on dark-and light-adapted Arabidopsis thylakoids indicate that the granal thylakoid lumen significantly expands in the light. Models generated for the organization of the oxygen-evolving complex within the granal lumen predict that the light-induced expansion greatly alleviates restrictions imposed on protein diffusion in this compartment in the dark. Experiments monitoring the redox kinetics of the luminal electron carrier plastocyanin support this prediction. The impact of the increase in protein mobility within the granal luminal compartment in the light on photosynthetic electron transport rates and processes associated with the repair of photodamaged photosystem II complexes is discussed.
引用
收藏
页码:20248 / 20253
页数:6
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