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用于大肠杆菌和产气荚膜梭菌的穿梭质粒。

Shuttle plasmids for Escherichia coli and Clostridium perfringens.

作者信息

Squires C H, Heefner D L, Evans R J, Kopp B J, Yarus M J

出版信息

J Bacteriol. 1984 Aug;159(2):465-71. doi: 10.1128/jb.159.2.465-471.1984.

Abstract

Small plasmids which replicate in both Escherichia coli and Clostridium perfringens were made by recombining E. coli plasmid pBR322 with three different small (less than 4 kilobases) plasmids native to C. perfringens. Subsequently, two homologous, though distinct, tetracycline resistance determinants (tet) from other C. perfringens plasmids were cloned into them. Both tet systems made E. coli resistant to at least 5 micrograms of tetracycline per ml when resident on the shuttle plasmids. The shuttle vectors have been used to transform L-phase variants and autoplasts of C. perfringens. In the latter case, the intact transforming plasmid could be isolated from walled cells after cell wall regeneration. Reciprocal transformation experiments in which plasmid DNAs derived from E. coli or C. perfringens were used suggest that restriction barriers exist between these two organisms. The plasmids contain restriction enzyme recognition sites in locations which are useful for cloning experiments.

摘要

通过将大肠杆菌质粒pBR322与产气荚膜梭菌的三种不同的小质粒(小于4千碱基)重组,构建了能在大肠杆菌和产气荚膜梭菌中复制的小质粒。随后,将来自其他产气荚膜梭菌质粒的两个同源但不同的四环素抗性决定子(tet)克隆到这些质粒中。当这两个tet系统存在于穿梭质粒上时,均可使大肠杆菌对每毫升至少5微克的四环素产生抗性。这些穿梭载体已用于转化产气荚膜梭菌的L型变体和原生质体。在后一种情况下,完整的转化质粒可在细胞壁再生后从有壁细胞中分离出来。使用源自大肠杆菌或产气荚膜梭菌的质粒DNA进行的相互转化实验表明,这两种生物体之间存在限制屏障。这些质粒在对克隆实验有用的位置含有限制酶识别位点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd7e/215668/917775860d18/jbacter00231-0041-a.jpg

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