Live-cell imaging of photosystem II antenna dissociation during state transitions

被引:101
作者
Iwai, Masakazu [1 ]
Yokono, Makio [1 ]
Inada, Noriko [2 ]
Minagawa, Jun [1 ]
机构
[1] Hokkaido Univ, Inst Low Temp Sci, Sapporo, Hokkaido 0600819, Japan
[2] Nara Inst Sci & Technol, Grad Sch Biol Sci, Nara 6300192, Japan
基金
日本学术振兴会; 日本科学技术振兴机构;
关键词
photosynthesis; fluorescence lifetime imaging microscopy; green algae; light-harvesting; energy dissipation; LIGHT-HARVESTING-COMPLEX; EXCITATION-ENERGY TRANSFER; CHLOROPHYLL-PROTEIN COMPLEX; CHLAMYDOMONAS-REINHARDTII; THYLAKOID MEMBRANE; FLUORESCENCE SPECTROSCOPY; ARABIDOPSIS-THALIANA; PHOSPHORYLATION; CHLOROPLAST; POLYPEPTIDES;
D O I
10.1073/pnas.0908808107
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
Plants and green algae maintain efficient photosynthesis under changing light environments by adjusting their light-harvesting capacity. It has been suggested that energy redistribution is brought about by shuttling the light-harvesting antenna complex II (LHCII) between photosystem II (PSII) and photosystem I (PSI) (state transitions), but such molecular remodeling has never been demonstrated in vivo. Here, using chlorophyll fluorescence lifetime imaging microscopy, we visualized phospho-LHCII dissociation from PSII in live cells of the green alga Chlamydomonas reinhardtii. Induction of energy redistribution in wild-type cells led to an increase in, and spreading of, a 250-ps lifetime chlorophyll fluorescence component, which was not observed in the stt7 mutant incapable of state transitions. The 250-ps component was also the dominant component in a mutant containing the light-harvesting antenna complexes but no photosystems. The appearance of the 250-ps component was accompanied by activation of LHCII phosphorylation, supporting the visualization of phospho-LHCII dissociation. Possible implications of the unbound phospho-LHCII on energy dissipation are discussed.
引用
收藏
页码:2337 / 2342
页数:6
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