首页> 外文OA文献 >A COMPARISON OF CHLOROPLAST MEMBRANE SURFACES VISUALIZED BY FREEZE-ETCH AND NEGATIVE STAINING TECHNIQUES; AND ULTRASTRUCTURAL CHARACTERIZATION OF MEMBRANE FRACTIONS OBTAINED FROM DIGITONIN-TREATED SPINACH CHLOROPLASTS
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A COMPARISON OF CHLOROPLAST MEMBRANE SURFACES VISUALIZED BY FREEZE-ETCH AND NEGATIVE STAINING TECHNIQUES; AND ULTRASTRUCTURAL CHARACTERIZATION OF MEMBRANE FRACTIONS OBTAINED FROM DIGITONIN-TREATED SPINACH CHLOROPLASTS

机译:冻蚀和负染色技术可视化的叶绿体膜表面的比较洋地黄处理过的菠菜叶绿体的膜分离及其超微结构表征

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摘要

Spinach chloroplast lamellae were washed free of negatively staining surface particles (carboxydismutase and coupling factor protein) and the resulting smooth-surfaced lamellae still showed the usual large (175 A) and small (110 A) particles seen by freeze-etching. Therefore, the freeze-fracture plane probably occurs along an internal surface of the chloroplast membrane. Fractions obtained by differential centrifugation of digitonin-treated chloroplast membranes were studied by negative staining, thin sectioning, and freeze-etching techniques for electron microscopy. The material sedimenting between 1,000 g and 10,000 g, enriched in photosystem II activity, was shown to consist of membrane fragments. These freeze-etched membrane fragments were found to have large particles on most of the exposed fracture faces. The large particles had the same size and distribution pattern as the 175 A particles seen in intact chloroplast membranes. The material sedimenting between 50,000 g and 144,000 g, which had only photosystem I activity, was found to consist of particles in various degrees of aggregation. Freeze-etching of this fraction revealed only small particles corresponding to the 110 A particles seen in intact chloroplasts. A model is presented suggesting that chloroplast lamellar membranes have a binary structure, which digitonin splits into two components. The two membrane fragments have different structures, revealed by freeze-etching, and different photochemical and biochemical functions.
机译:菠菜叶绿体薄片洗净后没有负染的表面颗粒(羧基歧化酶和偶联因子蛋白),所得的光滑表面薄片仍显示出通常的大(175 A)和小(110 A)颗粒(通过冷冻蚀刻)。因此,冻结断裂面可能沿着叶绿体膜的内表面发生。通过负染色,薄切片和电子显微镜的冷冻蚀刻技术研究了用洋地黄素处理过的叶绿体膜进行差速离心得到的馏分。沉积在1,000 g和10,000 g之间的物质(富含光系统II活性)显示为由膜碎片组成。发现这些冷冻蚀刻的膜碎片在大多数暴露的断裂面上具有大颗粒。大颗粒具有与完整叶绿体膜中看到的175 A颗粒相同的大小和分布模式。发现沉积物在50,000 g至144,000 g之间,仅具有光系统I活性,发现该物质由不同聚集程度的颗粒组成。冷冻蚀刻该级分后,仅发现与完整叶绿体中所见的110 A颗粒相对应的小颗粒。提出的模型表明叶绿体层状膜具有二元结构,其洋地黄皂苷分裂成两个成分。这两个膜片段具有不同的结构(通过冷冻蚀刻显示)以及不同的光化学和生化功能。

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