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New ccdB positive-selection cloning vectors with kanamycin or chloramphenicol selectable markers.

Author information

Affiliations

  • 1. Département de Biologie Moléculaire, Université Libre de Bruxelles, Rhode-Saint-Genèse, Belgium.
      Authors
    • Bernard P 1
    (1 author)

Gene, 01 Aug 1995, 162(1):159-160
https://doi.org/10.1016/0378-1119(95)00314-v PMID: 7557407 

Abstract 

Recently, we described pKIL18/19 positive-selection cloning vectors which rely on the inactivation of the cytotoxic ccdB gene [Bernard et al., Gene 148 (1994) 71-74]. They are new tools for simplifying gene cloning/sequencing procedures, as only recombinant DNA allow the formation of viable colonies. To enhance positive-selection capabilities, putative translational reinitiation codons located within the pKIL18/19 ccdB were modified by site-directed mutagenesis. New pKIL-derived vectors with kanamycin (KmR) or chloramphenicol (CmR) resistance-encoding genes were also constructed. In addition, a new host derived from the DH2 strain was developed.

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Read article at publisher's site: https://doi.org/10.1016/0378-1119(95)00314-v

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