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鸡白血病RNA聚合酶II的RNA合成活性不需要24,000道尔顿的亚基。

The 24,000 Da subunit is not required for the RNA synthesis activity of chicken leukemia RNA polymerase II.

作者信息

Chuang L F, Chuang R Y

机构信息

Department of Pharmacology, School of Medicine, University of California, Davis 95616.

出版信息

Biochimie. 1988 Oct;70(10):1397-400. doi: 10.1016/0300-9084(88)90011-9.

Abstract

The partially purified RNA polymerase II from chicken leukemia cells (Chuang R. Y., Chuang L. F. & Israel M. (1986) Biochem. Pharmacol. 35, 1293-1297) contained multiple subunits with molecular masses (in Da) ranging from 220,000 to 24,000, as shown by SDS-polyacrylamide gel electrophoresis. The enzyme was further purified through phosphocellulose column and fractions containing the enzyme activity were collected and concentrated 400-fold through a microconcentrator. The microconcentrator contained a membrane with a molecular weight cutoff around 30,000 and, hence, removed the 24,000 Da polypeptide from the enzyme. It was found that the resulting enzyme retained all the catalytic activity as compared to the enzyme preparation before the concentration step, suggesting that the stoichiometric amount of the 24,000 Da polypeptide is not required for RNA synthesis activity with a denatured DNA template.

摘要

从鸡白血病细胞中部分纯化得到的RNA聚合酶II(Chuang R. Y., Chuang L. F. & Israel M. (1986) Biochem. Pharmacol. 35, 1293 - 1297)经SDS-聚丙烯酰胺凝胶电泳显示,含有多个分子量(以道尔顿计)在220,000至24,000之间的亚基。该酶通过磷酸纤维素柱进一步纯化,收集含有酶活性的级分,并通过微浓缩器浓缩400倍。微浓缩器包含一个截留分子量约为30,000的膜,因此从酶中去除了24,000道尔顿的多肽。结果发现,与浓缩步骤前的酶制剂相比,所得的酶保留了所有催化活性,这表明对于以变性DNA模板进行的RNA合成活性而言,24,000道尔顿多肽的化学计量数量并非必需。

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