PgUGT95B2 preferentially metabolizes flavones/flavonols and has evolved independently from flavone/flavonol UGTs identified in Arabidopsis thaliana

Phytochemistry. 2019 Jan:157:184-193. doi: 10.1016/j.phytochem.2018.10.025. Epub 2018 Nov 9.

Abstract

UDP-dependent glycosyltransferases (UGTs) convert aglycones into more stable, bioactive, and structurally diverse glycosylated derivatives. Pomegranate (Punica granatum L.) produces various glycosylated phenolic metabolites, e.g. hydrolyzable tannins (HTs), anthocyanins, and flavonoids, and constitutes an excellent system for investigating the corresponding UGT activities. Here we report the cloning and functional characterization of a pomegranate UGT, PgUGT95B2, which is highly active towards flavones and flavonols and can glycosylate at more than one position in the substrate molecule. Particularly, PgUGT95B2 has the strongest activity towards tricetin (flavone with a tri-hydroxylated B-ring) and can act at the 4'-O position of its B-ring. In addition, PgUGT95B2 was able to glycosylate flavones present in pomegranate metabolite extracts. Conversely, PgUGT95B2 did not produce a galloylglucose ester (precursor for HT biosynthesis) or anthocyanins in enzyme assays. Our phylogenetic analysis suggested an independent evolution of PgUGT95B2 and flavone/flavonol UGTs identified in the model plant Arabidopsis thaliana through convergent evolution or gene loss.

Keywords: Flavone; Flavonol; Lythraceae; Pomegranate; Punica granatum; UDP-dependent glycosyltransferase; UGT.

MeSH terms

  • Arabidopsis / enzymology*
  • Evolution, Molecular*
  • Flavones / metabolism*
  • Flavonols / metabolism*
  • Glycosyltransferases / chemistry
  • Glycosyltransferases / metabolism*
  • Hydrogen Bonding
  • Hydrolysis
  • Lythraceae / enzymology*
  • Molecular Docking Simulation
  • Phylogeny
  • Protein Conformation
  • Substrate Specificity

Substances

  • Flavones
  • Flavonols
  • Glycosyltransferases