Non-heme iron enzyme-catalyzed complex transformations: Endoperoxidation, cyclopropanation, orthoester, oxidative C-C and C-S bond formation reactions in natural product biosynthesis

Adv Protein Chem Struct Biol. 2019:117:1-61. doi: 10.1016/bs.apcsb.2019.06.002. Epub 2019 Sep 23.

Abstract

Non-heme iron enzymes catalyze a wide range of chemical transformations, serving as one of the key types of tailoring enzymes in the biosynthesis of natural products. Hydroxylation reaction is the most common type of reactions catalyzed by these enzymes and hydroxylation reactions have been extensively investigated mechanistically. However, the mechanistic details for other types of transformations remain largely unknown or unexplored. In this paper, we present some of the most recently discovered transformations, including endoperoxidation, orthoester formation, cyclopropanation, oxidative C-C and C-S bond formation reactions. In addition, many of them are multi-functional enzymes, which further complicate their mechanistic investigations. In this work, we summarize their biosynthetic pathways, with special emphasis on the mechanistic details available for these newly discovered enzymes.

Publication types

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

MeSH terms

  • Biological Products / chemistry
  • Biological Products / metabolism*
  • Fungal Proteins
  • Fungi / enzymology*
  • Models, Molecular
  • Nonheme Iron Proteins / chemistry
  • Nonheme Iron Proteins / metabolism*
  • Protein Conformation

Substances

  • Biological Products
  • Fungal Proteins
  • Nonheme Iron Proteins