Quercetin production from rutin by a thermostable β-rutinosidase from Pyrococcus furiosus

Biotechnol Lett. 2012 Mar;34(3):483-9. doi: 10.1007/s10529-011-0786-2. Epub 2011 Nov 4.

Abstract

Pyrococcus furiosus β-glucosidase converted rutin to quercetin and rutinose disaccharide with a ratio of 1:1, with no glucose, L-rhamnose, and isoquercitrin, indicating that the enzyme is a β-rutinosidase. The specific activity for flavonoid glycosides followed the order of isoquercitrin > quercitrin > rutin. The conversion of rutin to quercetin was optimal at pH 5.0 and 95°C in the presence of 0.5% dimethyl sulfoxide with a half-life of 101 h, a k(cat) of 1.6 min(-1), and a K(m) of 0.3 mM. Under the improved conditions, the enzyme produced 6.5 mM quercetin from 10 mM rutin after 150 min, with a molar yield of 65% and a productivity of 2.6 mM/h. This productivity is the highest reported thus far among enzymatic transformations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Enzyme Stability
  • Glycoside Hydrolases / chemistry
  • Glycoside Hydrolases / isolation & purification*
  • Glycoside Hydrolases / metabolism*
  • Kinetics
  • Models, Molecular
  • Pyrococcus furiosus / enzymology*
  • Quercetin / metabolism*
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / isolation & purification
  • Recombinant Proteins / metabolism
  • Rutin / metabolism*
  • Substrate Specificity
  • Temperature

Substances

  • Recombinant Proteins
  • Rutin
  • Quercetin
  • Glycoside Hydrolases
  • beta-rutinosidase