Dissecting and exploiting intermodular communication in polyketide synthases

Science. 1999 Apr 16;284(5413):482-5. doi: 10.1126/science.284.5413.482.

Abstract

Modular polyketide synthases catalyze the biosynthesis of medicinally important natural products through an assembly-line mechanism. Although these megasynthases display very precise overall selectivity, we show that their constituent modules are remarkably tolerant toward diverse incoming acyl chains. By appropriate engineering of linkers, which exist within and between polypeptides, it is possible to exploit this tolerance to facilitate the transfer of biosynthetic intermediates between unnaturally linked modules. This protein engineering strategy also provides insights into the evolution of modular polyketide synthases.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Catalysis
  • Escherichia coli / enzymology
  • Escherichia coli / genetics
  • Evolution, Molecular
  • Genes, Bacterial
  • Lactones / metabolism*
  • Macrolides / metabolism
  • Molecular Sequence Data
  • Multienzyme Complexes / chemistry*
  • Multienzyme Complexes / genetics
  • Multienzyme Complexes / metabolism*
  • Nuclear Magnetic Resonance, Biomolecular
  • Peptides / metabolism
  • Protein Engineering*
  • Recombinant Fusion Proteins / chemistry
  • Recombinant Fusion Proteins / metabolism
  • Streptomyces / enzymology

Substances

  • Lactones
  • Macrolides
  • Multienzyme Complexes
  • Peptides
  • Recombinant Fusion Proteins