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Genetic analysis of the gentamicin resistance region of pPH1JI and incorporation into a wide host range cloning vehicle.

作者信息

Rubin R A

机构信息

BioTechnica International, Inc., Cambridge, Massachusetts 02140.

出版信息

Plasmid. 1987 Jul;18(1):84-8. doi: 10.1016/0147-619x(87)90081-3.

Abstract

A region of the IncP plasmid pPH1JI encoding resistance to gentamicin, spectinomycin, and streptomycin was characterized by subcloning, deletion, and insertion mutagenesis. Approximate locations of these resistance determinants were established. A 1.6-kb HindIII-SphI segment of this region expresses gentamicin resistance (Gmr) in Escherichia coli when inserted into various plasmid vectors; this DNA segment encodes a polypeptide of 17.5 kDa. Incorporation of this fragment into an IncP cloning vehicle produced a Gmr wide host range vector, pRAR209, which confers levels of Gmr comparable to those expressed by pPH1JI in E. coli, Agrobacterium tumefaciens, and Rhizobium meliloti.

摘要

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