Utilization of a reporter system based on the blue pigment indigoidine biosynthetic gene bpsA for detection of promoter activity and deletion of genes in Streptomyces

J Microbiol Methods. 2015 Jun:113:1-3. doi: 10.1016/j.mimet.2015.03.017. Epub 2015 Mar 20.

Abstract

The integrative promoter-probe plasmid pBPSA1 was constructed using a promoterless Streptomyces aureofaciens CCM3239 bpsA gene encoding a non-ribosomal peptide synthase for the biosynthesis of a blue pigment, indigoidine. bpsA was also used to prepare pAMR4 plasmid for the deletion of genes in Streptomyces with facile identification of double crossover recombination.

Keywords: Actinorhodin; Gene disruption; Indigoidine; Promoter-probe vector; Reporter gene; Streptomyces.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Genes, Bacterial*
  • Genes, Reporter*
  • Peptide Synthases / genetics
  • Piperidones / metabolism*
  • Plasmids
  • Promoter Regions, Genetic*
  • Recombination, Genetic
  • Sequence Deletion*
  • Streptomyces aureofaciens / enzymology
  • Streptomyces aureofaciens / genetics*

Substances

  • Piperidones
  • indigoidine
  • Peptide Synthases
  • non-ribosomal peptide synthase