Direct cloning and heterologous expression of the salinomycin biosynthetic gene cluster from Streptomyces albus DSM41398 in Streptomyces coelicolor A3(2)

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Jia Yin - , TUD Dresden University of Technology (Author)
  • Michael Hoffmann - (Author)
  • Xiaoying Bian - (Author)
  • Qiang Tu - (Author)
  • Fu Yan - (Author)
  • Liqiu Xia - (Author)
  • Xuezhi Ding - (Author)
  • A. Francis Stewart - , Chair of Applied Genomics (Author)
  • Rolf Müller - (Author)
  • Jun Fu - , TUD Dresden University of Technology (Author)
  • Youming Zhang - (Author)

Abstract

Linear plus linear homologous recombination-mediated recombineering (LLHR) is ideal for obtaining natural product biosynthetic gene clusters from pre-digested bacterial genomic DNA in one or two steps of recombineering. The natural product salinomycin has a potent and selective activity against cancer stem cells and is therefore a potential anti-cancer drug. Herein, we separately isolated three fragments of the salinomycin gene cluster (salO-orf18) from Streptomyces albus (S. albus) DSM41398 using LLHR and assembled them into intact gene cluster (106 kb) by Red/ET and expressed it in the heterologous host Streptomyces coelicolor (S. coelicolor) A3(2). We are the first to report a large genomic region from a Gram-positive strain has been cloned using LLHR. The successful reconstitution and heterologous expression of the salinomycin gene cluster offer an attractive system for studying the function of the individual genes and identifying novel and potential analogues of complex natural products in the recipient strain.

Details

Original languageEnglish
Article number15081
JournalScientific reports
Volume5
Publication statusPublished - 13 Oct 2015
Peer-reviewedYes

External IDs

PubMed 26459865
ORCID /0000-0002-4754-1707/work/142248099

Keywords

Sustainable Development Goals

ASJC Scopus subject areas