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酵母2微米质粒的FLP蛋白。从表达克隆的FLP基因的大肠杆菌细胞中纯化该蛋白。

The FLP protein of the 2-micron plasmid of yeast. Purification of the protein from Escherichia coli cells expressing the cloned FLP gene.

作者信息

Babineau D, Vetter D, Andrews B J, Gronostajski R M, Proteau G A, Beatty L G, Sadowski P D

出版信息

J Biol Chem. 1985 Oct 5;260(22):12313-9.

PMID:2995370
Abstract

Most laboratory strains of the yeast Saccharomyces cerevisiae contain many copies of an autonomously replicating plasmid called 2-micron circle DNA. This plasmid codes for a site-specific recombinase, the FLP protein which promotes recombination across two 599-base pair inverted repeats of the plasmid DNA. We have cloned the FLP gene under the control of a strong Escherichia coli promoter and have hyperproduced the protein in that organism. Cell-free extracts from this source promote highly efficient site-specific recombination in vitro and we have used this activity to purify the FLP protein substantially. The enzyme acts efficiently on circular and linear substrates and requires only monovalent or divalent cations for activity.

摘要

大多数酿酒酵母实验室菌株都含有许多名为2微米环状DNA的自主复制质粒拷贝。该质粒编码一种位点特异性重组酶,即FLP蛋白,它促进质粒DNA的两个599碱基对反向重复序列之间的重组。我们已在强大肠杆菌启动子的控制下克隆了FLP基因,并在该生物体中过量表达了该蛋白。来自该来源的无细胞提取物在体外促进高效的位点特异性重组,我们利用这种活性大量纯化了FLP蛋白。该酶对环状和线性底物均能高效发挥作用,并且仅需要单价或二价阳离子来发挥活性。

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