A ThDP-dependent enzymatic carboligation reaction involved in Neocarazostatin A tricyclic carbazole formation

Org Biomol Chem. 2016 Sep 21;14(37):8679-8684. doi: 10.1039/c6ob01651k.

Abstract

Although the biosynthetic pathway of Neocarazostatin A (1) has been identified, the detailed enzymatic reactions underlying the assembly of the carbazole ring still remain largely unknown. We demonstrate here that NzsH, a putative thiamine diphosphate dependent enzyme, can catalyze an acyloin coupling reaction between indole-3-pyruvate and pyruvate to generate a β-ketoacid intermediate. Our findings thus shed light on further characterization of the unusual biosynthetic pathway of the bacterial tricyclic carbazole alkaloids.

MeSH terms

  • Biosynthetic Pathways
  • Carbazoles / metabolism*
  • Genes, Bacterial
  • Indoles / metabolism
  • Kinetics
  • Multigene Family
  • Phylogeny
  • Pyruvic Acid / metabolism
  • Streptomyces / enzymology*
  • Streptomyces / genetics
  • Streptomyces / metabolism
  • Thiamine Pyrophosphate / metabolism*

Substances

  • Carbazoles
  • Indoles
  • neocarazostatin A
  • indol-3-yl pyruvic acid
  • Pyruvic Acid
  • Thiamine Pyrophosphate