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从大豆悬浮培养物的原生质体中分离质膜。

The isolation of plasma membrane from protoplasts of soybean suspension cultures.

作者信息

Galbraith D W, Northcote D H

出版信息

J Cell Sci. 1977 Apr;24:295-310. doi: 10.1242/jcs.24.1.295.

Abstract

A procedure for the isolation of plasma membranes from protoplasts of suspension-cultured soybean is described. Protoplasts were prepared by enzymic digestion of the cell wall and the plasma membrane was labelled with radioactive diazotized sulphanilic acid. The membrane systems from broken protoplasts were separated by continuous isopycnic sucrose gradient centrifugation. Radioactivity was localized in a band possessing a buoyant density of 1-14 g ml-1. The activities of NADPH- and NADH-cytochrome c reductase, fumarase, Mg2+-ATPase, IDPase and acid phosphodiesterase in the various regions of the density gradient were determined. A plasma membrane fraction was selected which was relatively uncontaminated with membranes derived from endoplasmic reticulum, tonoplasts and mitochondria. The results indicated that Mg2+-ATPase and possibly acid phosphodiesterase were associated with the plasma membrane.

摘要

本文描述了一种从悬浮培养的大豆原生质体中分离质膜的方法。通过酶解细胞壁制备原生质体,并用放射性重氮化磺胺酸标记质膜。破碎原生质体的膜系统通过连续等密度蔗糖梯度离心进行分离。放射性定位在一条浮力密度为1.14 g/ml的条带中。测定了密度梯度不同区域中NADPH-和NADH-细胞色素c还原酶、延胡索酸酶、Mg2+-ATP酶、IDP酶和酸性磷酸二酯酶的活性。选择了一个相对未受内质网、液泡膜和线粒体来源膜污染的质膜部分。结果表明,Mg2+-ATP酶以及可能的酸性磷酸二酯酶与质膜有关。

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