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在大肠杆菌中表达该基因后,直接证明四膜虫14纳米丝状蛋白/柠檬酸合酶的双功能特性。

Direct demonstration of the bifunctional property of Tetrahymena 14-nm filament protein/citrate synthase following expression of the gene in Escherichia coli.

作者信息

Takeda T, Watanabe Y, Numata O

机构信息

Institute of Biological Sciences, University of Tsukuba, Tsukuba, Ibaraki, 305, Japan.

出版信息

Biochem Biophys Res Commun. 1997 Aug 18;237(2):205-10. doi: 10.1006/bbrc.1997.7008.

Abstract

Tetrahymena 14-nm filament protein/citrate synthase (49K protein) is a bifunctional protein with roles in the cytoskeleton and as a citrate synthase. Though previous studies have shown that the 49K protein is derived from a single transcript of a single gene, direct demonstration of the 49K protein's bifunctional property remained to be elucidated. In this study, a recombinant 49K protein was expressed in Escherichia coli, purified and characterized. The citrate synthase activity of the recombinant 49K protein was comparable to that of the 49K protein purified from Tetrahymena. The recombinant 49K protein formed 14-nm filaments, but only of short length. The filaments were elongated in the presence of a soluble fraction of Tetrahymena. These results suggest that the 49K protein itself is bifunctional, but some co-factor(s) is necessary for elongation of filaments.

摘要

嗜热四膜虫14纳米丝蛋白/柠檬酸合酶(49K蛋白)是一种双功能蛋白,在细胞骨架中发挥作用并作为柠檬酸合酶。尽管先前的研究表明49K蛋白源自单个基因的单个转录本,但49K蛋白双功能特性的直接证明仍有待阐明。在本研究中,重组49K蛋白在大肠杆菌中表达、纯化并进行了表征。重组49K蛋白的柠檬酸合酶活性与从嗜热四膜虫中纯化的49K蛋白相当。重组49K蛋白形成了14纳米的丝,但长度较短。在嗜热四膜虫的可溶部分存在的情况下,这些丝会伸长。这些结果表明49K蛋白本身具有双功能,但丝的伸长需要一些辅助因子。

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