Characterization of the lnmKLM genes unveiling key intermediates for β-alkylation in leinamycin biosynthesis

Org Lett. 2011 Feb 4;13(3):498-501. doi: 10.1021/ol102838y. Epub 2010 Dec 30.

Abstract

Leinamycin (LNM, 1) biosynthesis is proposed to involve β-alkylation of the polyketide intermediate, catalyzed by LnmKLM. Inactivation of lnmK, lnmL, or lnmM afforded mutant strains that accumulated LNM K-1 (2), K-2 (3), K-3 (4), and isomers LNM K-1' (5), K-2' (6), and K-3' (7) whose polyketide origin was established by feeding experiments with sodium [1-(13)C]acetate. These findings confirm the indispensability of LnmKLM in 1 biosynthesis and suggest that β-alkylation proceeds on the growing polyketide intermediate while bound to the LNM polyketide synthase.

Publication types

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

MeSH terms

  • Alkylation
  • Lactams / chemical synthesis*
  • Macrolides / chemical synthesis*
  • Molecular Structure
  • Polyketide Synthases / genetics
  • Polyketide Synthases / metabolism*
  • Stereoisomerism
  • Streptomyces / chemistry
  • Streptomyces / genetics
  • Thiazoles / chemical synthesis*
  • Thiones / chemical synthesis*

Substances

  • Lactams
  • Macrolides
  • Thiazoles
  • Thiones
  • leinamycin
  • Polyketide Synthases