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. 1993 Aug 16;130(1):127-30.
doi: 10.1016/0378-1119(93)90355-7.

Construction of new Campylobacter cloning vectors and a new mutational cat cassette

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Construction of new Campylobacter cloning vectors and a new mutational cat cassette (VSports最新版本)

R Yao et al. Gene. .

"VSports" Abstract

We have developed new Campylobacter shuttle vectors which are 6. 5-6. 8-kb plasmids carrying Campylobacter and Escherichia coli replicons, a multiple cloning site (MCS), the lacZ alpha gene, oriT and either a kanamycin or chloramphenicol resistance-encoding gene (KmR or CmR) from Campylobacter which functions in both hosts. These vectors can be mobilized efficiently from E. coli into C. jejuni or C. coli, and stably maintained in these hosts. Plasmids pRY107 and pRY108 carry a KmR marker and 17 unique cloning sites in two different orientations in lacZ alpha, allowing easy blue/white color selection. Plasmids pRY111 and pRY112 contain a CmR gene and 17 unique sites in both orientations VSports手机版. In addition, MCS are flanked by T7 and T3 late promoters and M13 forward and reverse primer sites, facilitating expression in T7 or T3 expression systems and sequence analysis. A Campylobacter CmR gene cartridge, bracketed by six restriction sites, has been developed for use in site-specific mutagenesis of Campylobacter genes. .

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