Abstract

We have constructed chimeric plasmid vectors, pHY460 and pHY310, from the streptococcal tetracycline resistance (Tc R) plasmid pAMα1 (9.2kb) and the Escherichia coli vector pACYC177 (3.7kb). These bifunctional plasmids can replicate and express the Tc R gene in both E. coli and Bacillus subtilis. Plasmids pHY460 (7.0 kb) and pHY310 (4.8 kb) contain the Tc R gene of pAMα1 and the ampicillin resistance (Ap R) gene of pACYC177. Both plasmids showed high transformation efficiency in both host cells. pHY460 was maintained stably in B. subtilis and, thus, is a useful shuttle vector functioning in E. coli and B. subtilis. The PvuI, PstI, BglI and BanI sites in the Ap R gene and the HpaI, BalI and EcoRV sites in the Tc R gene can be used for selection of recombinant plasmids by insertional inactivation. In addition, plasmid pHY460 has unique sites for SacII, BstEII, XbaI, AvaI and BamHI.

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