Hybrid peptide-polyketide natural products: biosynthesis and prospects toward engineering novel molecules

Metab Eng. 2001 Jan;3(1):78-95. doi: 10.1006/mben.2000.0171.

Abstract

The structural and catalytic similarities between modular nonribosomal peptide synthetase (NRPS) and polyketide synthase (PKS) inspired us to search for hybrid NRPS-PKS systems. By examining the biochemical and genetic data known to date for the biosynthesis of hybrid peptide-polyketide natural products, we show (1) that the same catalytic sites are conserved between the hybrid NRPS-PKS and normal NRPS or PKS systems, although the ketoacyl synthase domain in NRPS/PKS hybrids is unique, and (2) that specific interpolypeptide linkers exist at both the C- and N-termini of the NRPS and PKS proteins, which presumably play a critical role in facilitating the transfer of the growing peptide or polyketide intermediate between NRPS and PKS modules in hybrid NRPS-PKS systems. These findings provide new insights for intermodular communications in hybrid NRPS-PKS systems and should now be taken into consideration in engineering hybrid peptide-polyketide biosynthetic pathways for making novel "unnatural" natural products.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Biological Products / biosynthesis*
  • Biological Products / chemical synthesis*
  • Biological Products / genetics
  • Carbohydrate Sequence
  • Molecular Sequence Data
  • Multienzyme Complexes / metabolism*
  • Peptide Synthases / biosynthesis*
  • Protein Engineering / methods*
  • Protein Engineering / trends

Substances

  • Biological Products
  • Multienzyme Complexes
  • Peptide Synthases
  • non-ribosomal peptide synthase