• Title of article

    α-Rhamnosidase activity in the marine isolate Novosphingobium sp. PP1Y and its use in the bioconversion of flavonoids

  • Author/Authors

    Izzo، نويسنده , , Viviana and Tedesco، نويسنده , , Pietro and Notomista، نويسنده , , Eugenio and Pagnotta، نويسنده , , Eduardo and Di Donato، نويسنده , , Alberto and Trincone، نويسنده , , Antonio and Tramice، نويسنده , , Annabella، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2014
  • Pages
    9
  • From page
    95
  • To page
    103
  • Abstract
    Crude protein extracts of Novosphingobium sp. PP1Y, a microorganism isolated from polluted marine waters in Pozzuoli (Italy), were analyzed for the presence of glycosidase activities. Particular attention was devoted to a α-L-rhamnosidase activity able to hydrolyze several flavonoids of interest for the pharmaceutical and food industries. This activity had an alkaline pH optimum and a moderate tolerance to the presence of organic solvents, appealing features for its possible biotechnological uses. An increase of the α-L-rhamnosidase activity in PP1Y crude extracts was induced by adding naringin to the growth medium, suggesting the possibility to use material from Citrus industrial waste to induce the glycosidase activity expressed by strain PP1Y and produce simultaneously high-added-value molecules from the hydrolysis of their flavonoids. In order to investigate on the enzymatic mechanism of PP1Y α-L-rhamnosidase activity, hydrolysis products of PNP-α-L-rhamnopyranoside were analyzed by 1H-NMR experiments. The kinetic behaviour clearly indicated an inverting mechanism of hydrolysis for this novel enzymatic activity.
  • Keywords
    Flavonoids bioconversion , ?-L-rhamnosidase , Novosphingobium sp. PP1Y
  • Journal title
    Journal of Molecular Catalysis B Enzymatic
  • Serial Year
    2014
  • Journal title
    Journal of Molecular Catalysis B Enzymatic
  • Record number

    1718863