Biochemical characterization of an intracellular 6G-fructofuranosidase from Xanthophyllomyces dendrorhous and its use in production of neo-fructooligosaccharides (neo-FOSs)

Bioresour Technol. 2011 Jan;102(2):1715-21. doi: 10.1016/j.biortech.2010.08.033. Epub 2010 Aug 13.

Abstract

An intracellular 6G-fructofuranosidase (endo-type enzyme) extracted from Xanthophyllomyces dendrorhous 269 efficiently hydrolyzes fructosyl-β-(2→1)-linked sucrose to produce neo-kestose as a main transglycosylation product. The enzyme with a molecular weight of 33 kDa was purified by DEAE-52 cellulose chromatography. Thirty-fivefold purification and a 13.4% enzyme activity recovery were achieved. Optimum enzyme activity occurred at pH 6.4 and 45 °C and the enzyme was stable at pH 4-7 and at 45 °C. Using sucrose as a substrate, the Km and Vmax values were, respectively, 511 mmol/l and 233 μmol/(min mg) for transfer activity and 62 mmol/l and 164 μmol/(min mg) for hydrolytic activity. Under optimum conditions, a maximum concentration (73.9 g/l) of neo-fructooligosaccharides catalyzed by the endo-enzyme was obtained. These findings suggest that the purified endo-enzyme exhibits a high transfructosylation activity and it has potential for the industrial production of neo-FOSs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Basidiomycota / drug effects
  • Basidiomycota / enzymology*
  • Chromatography, Ion Exchange
  • Electrophoresis, Polyacrylamide Gel
  • Enzyme Stability / drug effects
  • Hydrogen-Ion Concentration / drug effects
  • Indicators and Reagents / pharmacology
  • Intracellular Space / drug effects
  • Intracellular Space / enzymology*
  • Ions
  • Kinetics
  • Metals / pharmacology
  • Oligosaccharides / biosynthesis*
  • Sucrose / metabolism
  • Temperature
  • beta-Fructofuranosidase / isolation & purification
  • beta-Fructofuranosidase / metabolism*

Substances

  • Indicators and Reagents
  • Ions
  • Metals
  • Oligosaccharides
  • fructooligosaccharide
  • Sucrose
  • beta-Fructofuranosidase