| 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 |
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