Plasmid transfer from Streptomyces to Mycobacterium smegmatis by spontaneous transformation

Mol Microbiol. 2002 Jan;43(1):135-46. doi: 10.1046/j.1365-2958.2002.02722.x.

Abstract

Hybrids of the Streptomyces coelicolor conjugative plasmid SCP2* and the Mycobacterium plasmid pAL5000 were transferred from Streptomyces coelicolor or Streptomyces lividans to Mycobacterium smegmatis mc2155 in plate crosses. Inactivation of the SCP2* transfer function did not prevent or reduce plasmid transfer. This transfer was DNase I sensitive and thus involved release of DNA from Streptomyces, followed by transformation of M. smegmatis. M. smegmatis growing on specific solid media was also transformed by pure CCC and linear plasmid DNA. Small plasmids were taken up intact but large plasmids suffered deletions. Competence developed within 24 h of incubation at 30 degrees C or 37 degrees C, and up to 400 transformants were obtained per microg of CCC plasmid DNA. Transformation frequencies were higher when M. smegmatis was co-cultivated with plasmid-free Streptomyces, but unaffected by resident homologous sequences or inactivation of recA in M. smegmatis. Spontaneous transformation was also observed with a circular Streptomyces transposable element which inserted into chromosomal sites. Transformative plasmid transfer was also shown to occur between M. smegmatis strains. This is the first report of non-artificially induced, spontaneous plasmid transformation in Mycobacterium.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • DNA Replication
  • DNA Transposable Elements
  • DNA, Bacterial*
  • Deoxyribonuclease I
  • Mycobacterium smegmatis / genetics*
  • Mycobacterium smegmatis / growth & development
  • Plasmids*
  • Rec A Recombinases / metabolism
  • Sequence Deletion
  • Streptomyces / genetics*
  • Streptomyces / growth & development
  • Transformation, Bacterial*

Substances

  • DNA Transposable Elements
  • DNA, Bacterial
  • Rec A Recombinases
  • Deoxyribonuclease I