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奇异变形杆菌类recA基因的克隆

Cloning of a recA-like gene of Proteus mirabilis.

作者信息

Eitner G, Solonin A S, Tanyashin V I

出版信息

Gene. 1981 Sep;14(4):301-8. doi: 10.1016/0378-1119(81)90162-1.

Abstract

A gene of Proteus mirabilis that can substitute for functions of the recA gene of Escherichia coli has been cloned into the plasmid pBR322, using shotgun experiments. The recA-like gene (recAp.m.) has been localized by restriction mapping within a 1.5-Md PstI fragment that is a part of two cloned HindIII fragments of the chromosome of P. mirabilis. The restriction map of the recAp.m. gene differs from that of the recA gene of E. coli. Functionally, the recombinant plasmids containing the recAp.m. gene restore a nearly wild-type level of UV-resistance to several point and deletion mutants in the recA gene of E. coli.

摘要

通过鸟枪法实验,已将奇异变形杆菌中一个可替代大肠杆菌recA基因功能的基因克隆到质粒pBR322中。类recA基因(recAp.m.)已通过限制性酶切图谱定位在一个1.5兆道尔顿的PstI片段内,该片段是奇异变形杆菌染色体两个克隆的HindIII片段的一部分。recAp.m.基因的限制性酶切图谱与大肠杆菌recA基因的不同。在功能上,含有recAp.m.基因的重组质粒可使大肠杆菌recA基因的几个点突变体和缺失突变体恢复到接近野生型的紫外线抗性水平。

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