In vitro and in vivo manipulations of bacteriophage Mu DNA: cloning of Mu ends and construction of mini-Mu's carrying selectable markers

Gene. 1981 Jan-Feb;13(1):37-46. doi: 10.1016/0378-1119(81)90041-x.

Abstract

Recombinant plasmids carrying one or both ends of the bacteriophage Mu genome were constructed by molecular cloning. Transposable mini-Mu's with selectable markers (ampicillin resistance, kanamycin resistance or the entire lac operon of Escherichia coli) inserted between the Mu ends were also constructed. As a source of lac operon DNA, a pBR322 derivative with a 27 kb insert containing the lac operon was constructed. The plasmids with both ends of Mu (mini-Mu's) conferred full Mu immunity upon the host cells. However, the same mini-Mu's containing kan or lac inserts were defective in immunity. A summary of the construction and physical characterization, including restriction endonuclease cleavage maps and some of the biological properties of the plasmids, is presented.

Publication types

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

MeSH terms

  • Bacteriophage mu / genetics*
  • Cloning, Molecular / methods
  • DNA Restriction Enzymes
  • DNA Transposable Elements*
  • DNA, Recombinant
  • DNA, Viral / genetics*
  • Escherichia coli / genetics
  • Genetic Vectors
  • Lac Operon
  • Plasmids

Substances

  • DNA Transposable Elements
  • DNA, Recombinant
  • DNA, Viral
  • DNA Restriction Enzymes