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[处于液晶态的超螺旋DNA的酶促切割]

[Enzymatic cleavage of superhelical DNA in a liquid crystal state].

作者信息

Salianov V I, Palumbo M, Evdokimov Iu M

出版信息

Mol Biol (Mosk). 1992 Sep-Oct;26(5):1036-46.

PMID:1470171
Abstract

Superhelical pBR322 DNA molecules form liquid-crystalline dispersions in water-salt solutions containing poly(ethyleneglycol). The formation of the liquid-crystalline dispersions from superhelical DNA molecules results in the appearance of two sites inside the DNA molecules that are split by Micrococcal nuclease. The first site of digestion does not differ from the standard site split by this enzyme in water-salt solutions, whereas the second one represents a new site specific only for the DNA molecules forming liquid-crystalline dispersions. Splitting of the DNA molecule through the first site is accompanied by formation of its linear form; splitting of a new site results in the formation of two linear DNA fragments with molecular masses equal to half of the initial DNA molecules. Enzyme digestion of superhelical DNA molecules forming liquid-crystalline dispersions induces a reformation of the "nonspecific" space organization of dispersions to the cholesteric one. A hypothetic model for packing of the superhelical DNA molecules inside liquid-crystalline dispersions and its transformation under enzyme action is suggested.

摘要

超螺旋pBR322 DNA分子在含有聚乙二醇的水盐溶液中形成液晶分散体。超螺旋DNA分子形成液晶分散体导致DNA分子内部出现两个被微球菌核酸酶切割的位点。第一个切割位点与该酶在水盐溶液中切割的标准位点没有差异,而第二个位点是仅针对形成液晶分散体的DNA分子的新位点。通过第一个位点切割DNA分子伴随着其线性形式的形成;新位点的切割导致形成两个分子质量等于初始DNA分子一半的线性DNA片段。形成液晶分散体的超螺旋DNA分子的酶切诱导分散体的“非特异性”空间组织重新形成胆甾相。提出了一个关于超螺旋DNA分子在液晶分散体内堆积及其在酶作用下转化的假设模型。

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