Hirano_2005_Carbohydr.Res_340_2297

Reference

Title : Preparation of the methyl ester of hyaluronan and its enzymatic degradation - Hirano_2005_Carbohydr.Res_340_2297
Author(s) : Hirano K , Sakai S , Ishikawa T , Avci FY , Linhardt RJ , Toida T
Ref : Carbohydr Res , 340 :2297 , 2005
Abstract :

A methyl ester of hyaluronan in which the carboxyl groups were fully esterified was prepared using trimethylsilyl diazomethane. This derivative, while not depolymerized by hyaluronan lyases or hyaluronan hydrolases, was a substrate for both chondroitin ACI lyase (EC 4.2.2.5) from Flavobacterium heparinum and chondroitin ACII lyase (EC 4.2.2.5) from Arthrobacter aurescens. The major product isolated in these depolymerization reactions was methyl alpha-L-threo-hex-4-enepyranosyluronate-(1-->3)-2-acetamido-2-deoxy-alpha,beta-D- glucopyranoside as determined by 1H NMR spectroscopy and MALDITOF mass spectrometry.

PubMedSearch : Hirano_2005_Carbohydr.Res_340_2297
PubMedID: 16098492

Related information

Citations formats

Hirano K, Sakai S, Ishikawa T, Avci FY, Linhardt RJ, Toida T (2005)
Preparation of the methyl ester of hyaluronan and its enzymatic degradation
Carbohydr Res 340 :2297

Hirano K, Sakai S, Ishikawa T, Avci FY, Linhardt RJ, Toida T (2005)
Carbohydr Res 340 :2297