Oleszko S, Moudrianakis E N
J Cell Biol. 1974 Dec;63(3):936-48. doi: 10.1083/jcb.63.3.936.
Spinach chloroplast lamellae were stained with aqueous uranyl acetate immediately after glutaraldehyde-osmium fixation but before dehydration and embedding. Under these conditions, the lamellae are shown in thin sections to have 95-A x 115-A coupling factor particles on their surfaces. The particles can be seen only on the matrix side of nonopposed thylakoids, and are shown to occur on both stromal and granal lamellae, regardless of the organization of the lamellae into stacks. It is estimated that, in native, fully coupled chloroplast lamellae, there is on the average one coupling factor for every 500 chlorophyll molecules. The morphological appearance of the particles is not affected by a variety of buffers, by changes in illumination or temperature, or by alterations in the energy state of the membranes during preparation. The particles can be removed from the membranes with low concentrations of Na(2)EDTA, and the photophosphorylating activity of the membranes is concomitantly lost. Both the activity and the appearance of the particles can be restored to the membranes by rebinding EDTA-extracted coupling factors to the uncoupled membranes.
菠菜叶绿体片层在经戊二醛-锇固定后、脱水和包埋之前,立即用醋酸双氧铀水溶液染色。在这些条件下,薄片中的片层表面显示有95埃×115埃的偶联因子颗粒。这些颗粒仅能在未相对的类囊体的基质侧看到,并且显示无论片层是否堆叠,在基质片层和基粒片层上均有出现。据估计,在天然的、完全偶联的叶绿体片层中,平均每500个叶绿素分子有一个偶联因子。颗粒的形态外观不受多种缓冲液、光照或温度变化的影响,也不受制备过程中膜能量状态改变的影响。低浓度的Na₂EDTA可将颗粒从膜上除去,同时膜的光合磷酸化活性丧失。通过将EDTA提取的偶联因子重新结合到解偶联的膜上,颗粒的活性和外观均可恢复到膜上。