Acceptor specificity in the transglycosylation reaction using Endo-M

Carbohydr Res. 2010 Nov 22;345(17):2458-63. doi: 10.1016/j.carres.2010.08.022. Epub 2010 Sep 17.

Abstract

To determine the structural specificity of the glycosyl acceptor of the transglycosylation reaction using endo-β-N-acetylglucosaminidase (ENGase) (EC 3.2.1.96) from Mucor hiemalis (Endo-M), several acceptor derivatives were designed and synthesized. The narrow regions of the 1,3-diol structure from the 4- to 6-hydroxy functions of GlcNAc were found to be essential for the transglycosylation reaction using Endo-M. Furthermore, it was determined that Endo-M strictly recognizes a 1,3-diol structure consisting of primary and secondary hydroxyl groups.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromatography, High Pressure Liquid
  • Chromatography, Reverse-Phase
  • Glycosylation
  • Kinetics
  • Mannosyl-Glycoprotein Endo-beta-N-Acetylglucosaminidase / metabolism*
  • Mucor / enzymology
  • Oxygen / chemistry
  • Pyrans / chemistry
  • Substrate Specificity

Substances

  • Pyrans
  • Mannosyl-Glycoprotein Endo-beta-N-Acetylglucosaminidase
  • Oxygen