Purification and characterization of membrane-bound endoglycoceramidase from Corynebacterium sp

Eur J Biochem. 1992 Apr 15;205(2):729-35. doi: 10.1111/j.1432-1033.1992.tb16836.x.

Abstract

Endoglycoceramidase catalyzes the hydrolysis of the linkage between oligosaccharides and ceramides of various glycosphingolipids. We found that a bacterial strain Corynebacterium sp., isolated from soil, produced endoglycoceramidase both intracellularly and extracellularly. The intracellular enzyme bound to the cell membrane was solubilized with 1% Triton X-100 and purified to homogeneity about 170-fold with 60% recovery. The molecular mass of the enzyme was approximately 65 kDa. The enzyme is most active at pH 5.5-6.5 and stable at pH 3.5-8.0. Various neutral and acidic glycosphingolipids were hydrolyzed by the enzyme in the presence of 0.1% Triton X-100. Ganglio- and lacto-type glycosphingolipids were readily hydrolyzed, but globo-type glycosphingolipids were hydrolyzed slowly.

MeSH terms

  • Carbohydrate Sequence
  • Cations, Divalent
  • Cell Membrane / enzymology
  • Chromatography
  • Chromatography, DEAE-Cellulose
  • Chromatography, Gel
  • Corynebacterium / enzymology*
  • Detergents / pharmacology
  • Durapatite
  • Electrophoresis, Polyacrylamide Gel
  • Glycoside Hydrolases / isolation & purification*
  • Glycoside Hydrolases / metabolism*
  • Glycosphingolipids / metabolism*
  • Hydroxyapatites
  • Kinetics
  • Molecular Sequence Data
  • Molecular Weight
  • Spectrometry, Mass, Fast Atom Bombardment
  • Substrate Specificity

Substances

  • Cations, Divalent
  • Detergents
  • Glycosphingolipids
  • Hydroxyapatites
  • Durapatite
  • Glycoside Hydrolases
  • endoglycoceramidase