Efficient transposition in mycobacteria: construction of Mycobacterium smegmatis insertional mutant libraries

J Bacteriol. 1994 Jan;176(2):535-9. doi: 10.1128/jb.176.2.535-539.1994.

Abstract

The Tn611 transposon was inserted into pCG63, a temperature-sensitive plasmid isolated from an Escherichia coli-mycobacterial shuttle vector which contains the pAL5000 and pUC18 replicons. The resulting plasmid, pCG79, was used to generate a large number of insertional mutations in Mycobacterium smegmatis. These are the first mycobacterial insertional mutant libraries to be constructed by transposition directly into a mycobacterium. No highly preferential insertion sites were detected by Southern blot analysis of the chromosomal DNAs isolated from the insertion mutants. Auxotrophic mutants with various phenotypes were isolated at a frequency ranging from 0.1 to 0.4%, suggesting that the libraries are representative. The pCG79 system thus seems to be a useful tool for the study of M. smegmatis genetics and may be applicable to other mycobacteria, such as the M. tuberculosis complex.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acids / metabolism
  • Mutagenesis, Insertional / methods*
  • Mycobacterium / genetics*
  • Purines / metabolism
  • Vitamins / metabolism

Substances

  • Amino Acids
  • Purines
  • Vitamins