Nature's Combinatorial Biosynthesis Produces Vatiamides A-F

Angew Chem Int Ed Engl. 2019 Jul 1;58(27):9027-9031. doi: 10.1002/anie.201902571. Epub 2019 May 28.

Abstract

Hybrid type I PKS/NRPS biosynthetic pathways typically proceed in a collinear manner wherein one molecular building block is enzymatically incorporated in a sequence that corresponds to gene arrangement. In this work, genome mining combined with the use of a fluorogenic azide-based click probe led to the discovery and characterization of vatiamides A-F, three structurally diverse alkynylated lipopeptides, and their brominated analogues, from the cyanobacterium Moorea producens ASI16Jul14-2. These derive from a unique combinatorial non-collinear PKS/NRPS system encoded by a 90 kb gene cluster in which an upstream PKS cassette interacts with three separate cognate NRPS partners. This is facilitated by a series of promiscuous intermodule PKS-NRPS docking motifs possessing identical amino acid sequences. This interaction confers a new type of combinatorial capacity for creating molecular diversity in microbial systems.

Keywords: biosynthesis; combinatorial biosynthesis; cyanobacteria; non-ribosomal peptides; polyketides.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Amino Acid Sequence
  • Click Chemistry
  • Cyanobacteria / chemistry
  • Cyanobacteria / metabolism
  • Lipopeptides / biosynthesis*
  • Lipopeptides / chemistry
  • Multigene Family
  • Peptide Synthases / chemistry
  • Peptide Synthases / genetics
  • Peptide Synthases / metabolism*
  • Sequence Alignment

Substances

  • Lipopeptides
  • Peptide Synthases
  • non-ribosomal peptide synthase

Supplementary concepts

  • Moorea producens