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用于在脱硫弧菌中导入克隆DNA的新型穿梭载体。

New shuttle vectors for the introduction of cloned DNA in Desulfovibrio.

作者信息

Rousset M, Casalot L, Rapp-Giles B J, Dermoun Z, de Philip P, Bélaich J P, Wall J D

机构信息

Unité de Bioénergétique et Ingénierie des Proteines, CNRS, Marseille.

出版信息

Plasmid. 1998;39(2):114-22. doi: 10.1006/plas.1997.1321.

Abstract

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 sites, and colonies of recombinant clones can be identified by blue/white screening in E. coli. The pBMC, pBMK, and pBMS series carry the cat, 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.

摘要

将来自脱硫脱硫弧菌G100A隐蔽质粒的pBG1复制子插入pTZ18U衍生物中,以产生一个新的穿梭载体家族。这些质粒在大肠杆菌和脱硫弧菌中均稳定,具有大量独特的限制性酶切位点,并且重组克隆菌落可通过大肠杆菌中的蓝/白筛选来鉴定。pBMC、pBMK和pBMS系列分别携带cat、npt或strAB基因作为选择标记。pBMC6、pBMK6和pBMS6质粒可通过电转化导入脱硫脱硫弧菌和果糖脱硫弧菌,而pBMC7、pBMK7和pBMS7质粒含有额外的迁移功能,使其适合用于接合。

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