Beta-1,3-galactosyl-N-acetylhexosamine phosphorylase from Bifidobacterium bifidum DSM 20082: characterization, partial purification and relation to mucin degradation

Biotechnol Appl Biochem. 1999 Feb:29 ( Pt 1):3-10.

Abstract

A new enzyme has been characterized in a cell-free extract of Bifidobacterium bifidum that catalysed the reversible phosphorolytic cleavage of beta-1,3-galacto-oligosaccharides. In the presence of Pi, the phosphorolysis reaction was favoured and was accompanied by a Walden reaction. Cleavage of the beta-glycosidic linkage gave an alpha-galactoside derivative (alpha-D-galactose 1-phosphate). The enzyme possesses a high specificity for beta-D-galactosido-(1, 3)-N-acetylglucosamine and beta-D-galactosido-(1, 3)-N-acetylgalactosamine. This purified intracellular enzyme had an estimated molecular mass of 140 kDa. The galactophosphorolytic activity on disaccharides was optimal at pH 6-6.5 and the reverse reaction was optimal at pH 5.5-6. The temperature optimum for phosphorolysis and the reverse reaction was approx. 50-55 degrees C. This enzyme is of particular interest in degrading some beta-D-Gal(1, 3) linkages and should be classified as EC 2.4.1.-.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacterial Proteins / isolation & purification
  • Bacterial Proteins / metabolism
  • Bifidobacterium / enzymology*
  • Carbohydrate Conformation
  • Carbohydrate Sequence
  • Disaccharides / metabolism
  • Galactosephosphates / chemistry
  • Galactosephosphates / metabolism
  • Galactosyltransferases / chemistry
  • Galactosyltransferases / isolation & purification*
  • Galactosyltransferases / metabolism*
  • Hydrogen-Ion Concentration
  • Molecular Sequence Data
  • Mucins / metabolism*
  • Phosphorylation
  • Substrate Specificity
  • Swine
  • Temperature

Substances

  • Bacterial Proteins
  • Disaccharides
  • Galactosephosphates
  • Mucins
  • galactose-1-phosphate
  • Galactosyltransferases
  • beta-1,3-galactosyl-N-acetylhexosamine phosphorylase