Characterization of QmnD3/QmnD4 for double bond formation in quartromicin biosynthesis

Org Lett. 2014 Mar 21;16(6):1578-81. doi: 10.1021/ol500111n. Epub 2014 Feb 28.

Abstract

In this work, two enzymes responsible for the biogenesis of possible [4 + 2] reaction precursors in the quartromicin biosynthetic pathway were characterized: acetylation of 1 to yield 2 was catalyzed by QmnD3, and subsequent acetic acid elimination of 2 to form double bond product 3 was catalyzed by QmnD4. Site-directed mutagenesis assay of QmnD3 and QmnD4 was investigated, and a general base-catalyzed mechanism for QmnD4 is proposed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Fungal Proteins / metabolism
  • Furans / chemical synthesis*
  • Furans / chemistry
  • Hydrolases / metabolism*
  • Lipase / metabolism
  • Molecular Structure
  • Spiro Compounds / chemical synthesis*
  • Spiro Compounds / chemistry

Substances

  • Fungal Proteins
  • Furans
  • Spiro Compounds
  • quartromicin
  • Hydrolases
  • Lipase
  • lipase B, Candida antarctica