Bacterial type III polyketide synthases: phylogenetic analysis and potential for the production of novel secondary metabolites by heterologous expression in pseudomonads

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Frank Gross - , Saarland University, Technische Universität Carolo-Wilhelmina, Gesellschaft für Biotechnologische Forschung mbH (GBF) (Author)
  • Nora Luniak - , Saarland University (Author)
  • Olena Perlova - , Saarland University (Author)
  • Nikolaos Gaitatzis - , Saarland University, Biotica Technology Ltd (Author)
  • Holger Jenke-Kodama - , Humboldt University of Berlin (Author)
  • Klaus Gerth - , Gesellschaft für Biotechnologische Forschung mbH (GBF) (Author)
  • Daniela Gottschalk - , Technische Universität Carolo-Wilhelmina (Author)
  • Elke Dittmann - , Humboldt University of Berlin (Author)
  • Rolf Müller - , Saarland University, Technische Universität Carolo-Wilhelmina, Gesellschaft für Biotechnologische Forschung mbH (GBF) (Author)

Abstract

Type III polyketide synthases (PKS) were regarded as typical for plant secondary metabolism before they were found in microorganisms recently. Due to microbial genome sequencing efforts, more and more type III PKS are found, most of which of unknown function. In this manuscript, we report a comprehensive analysis of the phylogeny of bacterial type III PKS and report the expression of a type III PKS from the myxobacterium Sorangium cellulosum in pseudomonads. There is no precedent of a secondary metabolite that might be biosynthetically correlated to a type III PKS from any myxobacterium. Additionally, an inactivation mutant of the S. cellulosum gene shows no physiological difference compared to the wild-type strain which is why these type III PKS are assumed to be "silent" under the laboratory conditions administered. One type III PKS (SoceCHS1) was expressed in different Pseudomonas sp. after the heterologous expression in Escherichia coli failed. Cultures of recombinant Pseudomonas sp. harbouring SoceCHS1 turned red upon incubation and the diffusible pigment formed was identified as 2,5,7-trihydroxy-1,4-naphthoquinone, the autooxidation product of 1,3,6,8-tetrahydroxynaphthalene. The successful heterologous production of a secondary metabolite using a gene not expressed under administered laboratory conditions provides evidence for the usefulness of our approach to activate such secondary metabolite genes for the production of novel metabolites.

Details

Original languageEnglish
Pages (from-to)28-38
Number of pages11
JournalArchives of Microbiology
Volume185
Issue number1
Publication statusPublished - Mar 2006
Peer-reviewedYes
Externally publishedYes

External IDs

Scopus 33644552441

Keywords

Keywords

  • Acyltransferases/biosynthesis, Base Sequence, Myxococcales/enzymology, Naphthoquinones/chemistry, Phylogeny, Pseudomonas/genetics