Alkylating enzymes

Curr Opin Chem Biol. 2013 Apr;17(2):229-35. doi: 10.1016/j.cbpa.2013.02.016. Epub 2013 Mar 18.

Abstract

Chemospecific and regiospecific modifications of natural products by methyl, prenyl, or C-glycosyl moieties are a challenging and cumbersome task in organic synthesis. Because of the availability of an increasing number of stable and selective transferases and cofactor regeneration processes, enzyme-assisted strategies turn out to be promising alternatives to classical synthesis. Two categories of alkylating enzymes become increasingly relevant for applications: firstly prenyltransferases and terpene synthases (including terpene cyclases), which are used in the production of terpenoids such as artemisinin, or meroterpenoids like alkylated phenolics and indoles, and secondly methyltransferases, which modify flavonoids and alkaloids to yield products with a specific methylation pattern such as 7-O-methylaromadendrin and scopolamine.

Publication types

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

MeSH terms

  • Alkyl and Aryl Transferases / chemistry*
  • Alkyl and Aryl Transferases / metabolism*
  • Alkylation
  • Methyltransferases / chemistry*
  • Methyltransferases / metabolism*
  • Plant Proteins / chemistry
  • Plant Proteins / metabolism
  • Plants / enzymology

Substances

  • Plant Proteins
  • Methyltransferases
  • Alkyl and Aryl Transferases