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

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

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. 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.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Base Sequence
  • Campylobacter / enzymology
  • Campylobacter / genetics*
  • Campylobacter coli / enzymology
  • Campylobacter coli / genetics
  • Campylobacter jejuni / enzymology
  • Campylobacter jejuni / genetics
  • Chloramphenicol Resistance / genetics
  • Cloning, Molecular
  • DNA, Bacterial / analysis
  • Escherichia coli / genetics
  • Genes, Bacterial*
  • Genetic Vectors*
  • Kanamycin Resistance / genetics
  • Lac Operon
  • Molecular Sequence Data
  • Mutagenesis, Insertional / methods*
  • Mutagenesis, Site-Directed
  • Plasmids / genetics
  • Polymerase Chain Reaction
  • T-Phages / genetics

Substances

  • DNA, Bacterial