Sesquiterpene synthases: passive catalysts or active players?

Nat Prod Rep. 2012 Jan;29(1):60-71. doi: 10.1039/c1np00060h. Epub 2011 Nov 8.

Abstract

Sesquiterpene synthases catalyse the metal dependent turnover of farnesyl diphosphate to generate a class of natural products characterised by an enormous diversity in structure, stereochemistry, biological function and application. It has been proposed that these enzymes take a passive role in the reactions they catalyse and that they serve mostly as stereochemical templates, within which the reactions take place. Here, recent research into the structure and function of sesquiterpene synthases and the mechanisms of the reactions that they catalyse will be reviewed to suggest that these fascinating enzymes play multifaceted active roles in what are arguably the most complex biosynthetic reactions.

Publication types

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

MeSH terms

  • Alkyl and Aryl Transferases / chemistry
  • Alkyl and Aryl Transferases / metabolism*
  • Catalysis
  • Molecular Structure
  • Sesquiterpenes / chemistry
  • Sesquiterpenes / metabolism*

Substances

  • Sesquiterpenes
  • Alkyl and Aryl Transferases
  • terpene synthase