Combinatorial polyketide biosynthesis by de novo design and rearrangement of modular polyketide synthase genes

Nat Biotechnol. 2005 Sep;23(9):1171-6. doi: 10.1038/nbt1128. Epub 2005 Aug 14.

Abstract

Type I polyketide synthase (PKS) genes consist of modules approximately 3-6 kb long, which encode the structures of 2-carbon units in polyketide products. Alteration or replacement of individual PKS modules can lead to the biosynthesis of 'unnatural' natural products but existing techniques for this are time consuming. Here we describe a generic approach to the design of synthetic PKS genes where facile cassette assembly and interchange of modules and domains are facilitated by a repeated set of flanking restriction sites. To test the feasibility of this approach, we synthesized 14 modules from eight PKS clusters and associated them in 154 bimodular combinations spanning over 1.5-million bp of novel PKS gene sequences. Nearly half the combinations successfully mediated the biosynthesis of a polyketide in Escherichia coli, and all individual modules participated in productive bimodular combinations. This work provides a truly combinatorial approach for the production of polyketides.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Biotechnology / methods*
  • Combinatorial Chemistry Techniques
  • Escherichia coli / metabolism
  • Genetic Engineering / methods*
  • Lactones / chemistry
  • Macrolides / chemistry
  • Models, Chemical
  • Molecular Sequence Data
  • Plasmids / metabolism
  • Polyketide Synthases / biosynthesis
  • Polyketide Synthases / chemistry*
  • Protein Engineering / methods*
  • Protein Structure, Tertiary
  • Sequence Homology, Amino Acid

Substances

  • Lactones
  • Macrolides
  • Polyketide Synthases