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Developmental Loss of Photosystem II Activity and Structure in a Chloroplast-Encoded Tobacco Mutant Lutescens-1

机译:叶绿体编码的烟草突变体Lutescens-1中光系统II活性和结构的发育损失。

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摘要

Lutescens-1, a tobacco mutant with a maternally inherited dysfunction, displayed an unusual developmental phenotype. In vivo measurement of chlorophyll fluorescence revealed deterioration in photosystem II (PSII) function as leaves expanded. Analysis of thylakoid membrane proteins by polyacrylamide gel electrophoresis indicated the physical loss of nuclear- and chloroplast-encoded polypeptides comprising the PSII core complex concomitant with loss of activity. Freeze fracture electron micrographs of mutant thylakoids showed a reduced density, compared to wild type, of the EFs particles which have been shown previously to be the structural entity containing PSII core complexes and associated pigment-proteins. The selective loss of PSII cores from thylakoids resulted in a higher ratio of antenna chlorophyll to reaction centers and an altered 77 K chlorophyll fluorescence emission spectra; these data are interpreted to indicate functional isolation of light-harvesting chlorophyll a/b complexes in the absence of PSII centers. Examination of PSII reaction centers (which were present at lower levels in mutant membranes) by monitoring the light-dependent phosphorylation of PSII polypeptides and flash-induced O2 evolution patterns demonstrated that the PSII cores which were assembled in mutant thylakoids were functionally identical to those of wild type. We conclude that the lutescens-1 mutation affected the correct stoichiometry of PSII centers, in relation to other membrane constituents, by disrupting the proper assembly and maintenance of PSII complexes in lutescens-1 thylakoid membranes.
机译:具有母体遗传性功能障碍的烟草突变体Lutescens-1显示出异常的发育表型。叶绿素荧光的体内测量显示,随着叶片的扩展,光系统II(PSII)功能的恶化。通过聚丙烯酰胺凝胶电泳对类囊体膜蛋白的分析表明,包含PSII核心复合物的核和叶绿体编码多肽的物理损失伴随活性丧失。与野生型相比,突变类囊体的冷冻断裂电子显微照片显示出密度降低的EFs颗粒,EFs颗粒先前已证明是包含PSII核心复合物和相关色素蛋白的结构实体。类囊体中PSII核心的选择性损失导致触角叶绿素与反应中心的比率更高,并且改变了77 K的叶绿素荧光发射光谱;这些数据被解释为表明在没有PSII中心的情况下光捕获叶绿素a / b复合物的功能分离。通过监测PSII多肽的光依赖性磷酸化和闪烁诱导的O2进化模式,检查PSII反应中心(在突变膜中的水平较低),证明在突变类囊体中组装的PSII核心在功能上与那些野生型。我们得出的结论是,lutescens-1突变通过破坏lutescens-1类囊体膜中PSII复合物的正确组装和维持,影响了PSII中心相对于其他膜成分的正确化学计量。

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