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来自花椰菜花序的DNA依赖性RNA聚合酶II的大规模纯化及亚基结构

Large-scale purification and subunit structure of DNA-dependent RNA polymerase II from cauliflower inflorescence.

作者信息

Goto H, Sasaki Y, Kamikubo T

出版信息

Biochim Biophys Acta. 1978 Jan 26;517(1):195-204. doi: 10.1016/0005-2787(78)90047-3.

Abstract

DNA-dependent RNA polymerase II (nucleosidetriphosphate:RNA nucleotidyltransferase, EC 2.7.7.6) from cauliflower inflorescence (Brassica oleracae, var. botrytis) was highly purified by polyethyleneimine treatment on a large scale. The solubilized enzyme was partially purified by polyethyleneimine fractionation and subjected to chromatography on DEAE-Sephadex and phosphocellulose, and subsequently to sedimentation in a glycerol gradient. The specific activity (231 nmol/mg per 10 min) of this enzyme was comparable to that reported for other purified eukaryotic RNA polymerases. Analysis of the purified RNA polymerase II by polyacrylamide gel electrophoresis under nondenaturing conditions revealed a single band. The subunit composition of the enzyme was analyzed by electrophoresis under denaturing conditions. The RNA polymerase II contained subunits with molecular weights and molar ratios (in parentheses) of 180 000(1), 130 000(2), 48 000(2), 25 000(4), and 19 500(4).

摘要

通过大规模聚乙烯亚胺处理,从花椰菜花序(甘蓝变种,花椰菜)中高度纯化了依赖DNA的RNA聚合酶II(核苷三磷酸:RNA核苷酸转移酶,EC 2.7.7.6)。溶解的酶通过聚乙烯亚胺分级分离进行部分纯化,然后在DEAE - 葡聚糖凝胶和磷酸纤维素上进行色谱分离,随后在甘油梯度中进行沉降。该酶的比活性(每10分钟231 nmol/mg)与其他纯化的真核RNA聚合酶报道的比活性相当。在非变性条件下通过聚丙烯酰胺凝胶电泳分析纯化的RNA聚合酶II,显示出一条带。在变性条件下通过电泳分析该酶的亚基组成。RNA聚合酶II包含分子量和摩尔比(括号内)分别为180 000(1)、130 000(2)、48 000(2)、25 000(4)和19 500(4)的亚基。

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