Discovery of a Unique Flavonoid Biosynthesis Mechanism in Fungi by Genome Mining

Angew Chem Int Ed Engl. 2023 Mar 13;62(12):e202215529. doi: 10.1002/anie.202215529. Epub 2023 Feb 9.

Abstract

Flavonoids are important plant natural products with variable structures and bioactivities. All known plant flavonoids are generated under the catalysis of a type III polyketide synthase (PKS) followed by a chalcone isomerase (CHI) and a flavone synthase (FNS). In this study, the biosynthetic gene cluster of chlorflavonin, a fungal flavonoid with acetolactate synthase inhibitory activity, was discovered using a self-resistance-gene-directed strategy. A novel flavonoid biosynthetic pathway in fungi was revealed. A core nonribosomal peptide synthetase-polyketide synthase (NRPS-PKS) is responsible for the generation of the key precursor chalcone. Then, a new type of CHI catalyzes the conversion of a chalcone into a flavanone by a histidine-mediated oxa-Michael addition mechanism. Finally, the desaturation of flavanone to flavone is catalyzed by a new type of FNS, a flavin mononucleotide (FMN)-dependent oxidoreductase.

Keywords: Biosynthesis; Filamentous Fungi; Flavonoids; NRPS-PKS Hybrids; Synthetic Biology.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chalcones*
  • Flavanones*
  • Flavones*
  • Fungi / metabolism
  • Peptide Synthases / metabolism
  • Polyketide Synthases / metabolism

Substances

  • Chalcones
  • Polyketide Synthases
  • Flavones
  • Flavanones
  • Peptide Synthases