Glycosidase activity in the post-ecdysial cuticle of the blue crab, Callinectes sapidus

Comp Biochem Physiol B Biochem Mol Biol. 2001 Apr;128(4):683-90. doi: 10.1016/s1096-4959(00)00363-8.

Abstract

We have previously demonstrated a marked change in sugar moieties of glycoproteins of the cuticle of the blue crab, Callinectes sapidus, between 0.5 and 3 h post-ecdysis. The present study has identified a glycosidase that appears in the cuticle during the early post-ecdysial hours. The enzyme has affinities for p-nitrophenyl derivatives of both N-acetylglucosamine and N-acetylgalactosamine. Both activities are competitively inhibited by chitobiose, suggesting that the enzyme could be a N-acetylhexosaminidase (EC 3.2.1.52). Atypical of N-acetylhexosaminidases described to date, this enzyme has a pH optimum of 7.0. The enzyme activity is high during the post-ecdysial period coincident with the changes in glycoprotein profiles observed in vivo. Partial purification of the enzyme has been accomplished by Sephacryl size-exclusion chromatography followed by concanavalin A affinity chromatography.

Publication types

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

MeSH terms

  • Acetylgalactosamine / analogs & derivatives*
  • Acetylgalactosamine / metabolism
  • Animals
  • Brachyura / enzymology*
  • Brachyura / physiology
  • Glycoside Hydrolases / chemistry
  • Glycoside Hydrolases / isolation & purification
  • Glycoside Hydrolases / metabolism*
  • Kinetics
  • Molting*
  • Substrate Specificity

Substances

  • 4-nitrophenyl-2-acetamido-2-deoxygalactopyranoside
  • Glycoside Hydrolases
  • Acetylgalactosamine