Characterization of the defective beta-glucuronidase activity in canine mucopolysaccharidosis type VII

Enzyme. 1989;42(3):174-80. doi: 10.1159/000469027.

Abstract

Canine mucopolysaccharidosis type VII results from deficient activity of lysosomal beta-glucuronidase. Residual enzymatic activity (0.2-1.7% of normal) was detected in tissue homogenates from affected dogs. In contrast, serum and urine from affected animals had up to 15% residual activity. To further characterize the nature of the defective enzyme, hepatic beta-glucuronidase was partially purified from normal and MPS VII dogs for determination of their physical and kinetic properties. About 65% of the total beta-glucuronidase in normal canine liver required detergent for solubilization (i.e., membrane-associated), whereas only 22% of the residual activity in canine MPS VII liver was membrane-associated. Compared to the normal hepatic enzyme, the Km towards 4-methylumbelliferyl-beta-glucuronide was markedly increased in MPS VII dogs (i.e., 0.48 versus greater than 2.5 mmol/l). In contrast, the thermo-, cryo-, and pH stability properties, as well as the pH optimum (approximately 4.6), were essentially unaffected. In addition, the canine MPS VII hepatic residual activity was unresponsive to sulfhydryl reducing reagents and divalent cations, despite the fact that incubation of normal canine beta-glucuronidase with dithiothreitol and magnesium and/or calcium enhanced the activity more than 15-fold.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Disease Models, Animal
  • Dog Diseases / enzymology*
  • Dog Diseases / genetics
  • Dogs
  • Enzyme Stability
  • Freezing
  • Glucuronidase / genetics*
  • Glucuronidase / isolation & purification
  • Glycosaminoglycans / metabolism
  • Hot Temperature
  • Hydrogen-Ion Concentration
  • Kinetics
  • Mucopolysaccharidoses / enzymology
  • Mucopolysaccharidoses / genetics
  • Mucopolysaccharidoses / veterinary*

Substances

  • Glycosaminoglycans
  • Glucuronidase