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单细胞莱茵衣藻室温叶绿素荧光发射带的重新分配。

Revised assignment of room-temperature chlorophyll fluorescence emission bands in single living cells of Chlamydomonas reinhardtii.

机构信息

Laboratory of Plant Cytophysiology, Department of Biology and Evolution, University of Ferrara, Italy.

出版信息

J Bioenerg Biomembr. 2011 Apr;43(2):163-73. doi: 10.1007/s10863-011-9343-x. Epub 2011 Feb 19.

Abstract

Room temperature (RT) microspectrofluorimetry in vivo of single cells has a great potential in photosynthesis studies. In order to get new information on RT chlorophyll fluorescence bands, we analyzed the spectra of Chlamydomonas reinhardtii mutants lacking fundamental proteins of the thylakoid membrane and spectra of photoinhibited WT cells. RT spectra of single living cells were characterized thorough derivative analyses and Gaussian deconvolution. The results obtained suggest that the dynamism in LHCII assembly could be sufficient to explain the variations in amplitudes of F680 (free LHCII), F694 (LHCII-PSII) and F702 (LHCII aggregates); F686 was assigned to the PSII core. Based on the revised assignments and on the variations observed, we discuss the meaning of the two fluorescence emission ratios F680/(F686 + F694) and F702/(F686 + F694), showing that these are sensitive parameters under moderate photoinhibition. In the most photoinhibited samples, the RT spectra tended to degenerate, showing characteristics of mutants that are partly depleted in PSII.

摘要

室温(RT)微光谱荧光在活细胞体内研究光合作用具有巨大的潜力。为了获取有关 RT 叶绿素荧光带的新信息,我们分析了缺乏类囊体膜基本蛋白的莱茵衣藻突变体的光谱和光抑制 WT 细胞的光谱。通过导数分析和高斯分解对单个活细胞的 RT 光谱进行了特征描述。结果表明,LHCII 组装的动态性足以解释 F680(游离 LHCII)、F694(LHCII-PSII)和 F702(LHCII 聚集体)的幅度变化;F686 被分配给 PSII 核心。基于修订后的分配和观察到的变化,我们讨论了两个荧光发射比 F680/(F686+F694)和 F702/(F686+F694)的意义,表明这些在中度光抑制下是敏感参数。在最受光抑制的样品中,RT 光谱趋于退化,表现出 PSII 部分耗尽的突变体的特征。

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