Structural diversity of decalin forming Diels-Alderase

Biosci Biotechnol Biochem. 2024 May 17:zbae040. doi: 10.1093/bbb/zbae040. Online ahead of print.

Abstract

The Diels-Alder (DA) reaction, specifically referring to the [4 + 2] cycloaddition reaction in pericyclic reactions, is a process that forms two carbon-carbon covalent bonds in a single step via an electron ring transition state. Among the secondary metabolites produced by microorganisms, numerous compounds are biosynthesized through DA reactions, most of which are enzymatic. Our research group has discovered an enzyme named Diels-Alderase (DAase) that catalyzes the DA reaction in filamentous fungi, and we have been investigating its catalytic mechanism. This review describes the reported microbial DAase enzymes, with a particular focus on those involved in the construction of the decalin ring.

Keywords: Diels–Alder reaction; natural product biosynthesis; nonribosomal peptide synthetase; polyketide synthase; stereoselective reaction.