New shuttle vectors for the introduction of cloned DNA in Desulfovibrio

被引:40
作者
Rousset, M
Casalot, L
Rapp-Giles, BJ
Dermoun, Z
de Philip, P
Bélaich, JP
Wall, JD
机构
[1] CNRS, Unite Bioenerget & Ingn Prot, F-13402 Marseille 20, France
[2] Univ Missouri, Dept Biochem, Columbia, MO 65201 USA
[3] Univ Aix Marseille 1, F-1331 Marseille 20, France
关键词
plasmid; cloning vector; electrotransformation; electroporation; conjugation; mobilization function;
D O I
10.1006/plas.1997.1321
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The pBG1 replicon from the cryptic plasmid of Desulfovibrio desulfuricans G100A was inserted into pTZ18U derivatives to generate a new family of shuttle vectors. These plasmids are stable both in Escherichia coli and in Desulfovibrio, they present a large number of unique restriction sires, and colonies of recombinant clones can be identified by blue/white screening in E. coli. The pBMC, pBMK, and pBMS series carry the car, npt, or strAB genes as selectable markers, respectively. The pBMC6, pBMK6, and pBMS6 plasmids can be introduced both in D. desulfuricans and in Desulfovibrio fructosovorans by electrotransformation, and the pBMC7, pBMK7, and pBMS7 plasmids contain additional mobilization functions which makes them suitable for conjugation. (C) 1998 Academic Press.
引用
收藏
页码:114 / 122
页数:9
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