Mechanistic insights into Diels-Alder reactions in natural product biosynthesis

Curr Opin Chem Biol. 2016 Dec:35:117-123. doi: 10.1016/j.cbpa.2016.09.015. Epub 2016 Sep 30.

Abstract

Natural enzymes that catalyze Diels-Alder reactions have long been sought after, yet few enzymes have been experimentally confirmed to perform this reaction. In the past five years, several stand-alone enzymes that can catalyze the Diels-Alder reaction had been identified and characterized. Among which, the crystal structures of SpnF, PyrI4 and AbyU have been determined. The structures of PyrI4 and AbyU, which are involved in spirotetronate/spirotetramate biosynthesis, are particularly informative since they shed light on how a natural catalyst captures the flexible substrate and facilitates the intramolecular Diels-Alder reaction through stabilization of the transition state in catalysis. These pioneering studies will inspire the design of artificial catalysts for Diels-Alder reactions.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Biological Products / chemistry
  • Biological Products / metabolism*
  • Crystallography, X-Ray
  • Cycloaddition Reaction
  • Enzymes / chemistry
  • Enzymes / metabolism
  • Protein Conformation
  • Sequence Homology, Amino Acid

Substances

  • Biological Products
  • Enzymes