원문정보
초록
영어
[a,a]-Trehalose was efficiently modified by a transgalactosylation reaction of Escherichia coli B-galactosidase using lactose as a donor to yield two galactosyl trehalose trisaccharides. The reaction products of trehalose by the enzyme were observed by thin layer chromatography (TLC) and high performance anion exchange chromatography (HPAEC) and were purified by BioGel P2 gel permeation chromatography and recycling preparative HPLC. Liquid chromatography-mass spectrometry (LC-MS) and 13C$ nuclear magnetic resonance (NMR) analyses revealed that the structures of the main products were 62-B-D-galactosy1 trehalose (1) and 42-B-D-galactosy1 trehalose (2). A reaction of 30%(w/v) trehalose and 15%(w/v) lactose at pH 7.5 and resulted in a total yield of approximately 27-30% based on the amount of trehalose used. The galactosyl trehalose products were not hydrolyzed by trehalose. In addition the mixture of transfer products (9:1 ratio of 1 to 2) showed higher thermal stability than glucose, lactose, and maltose, but less than trehalose, against heat treatment over at pH 4 and 7. It also exhibited better thermal stability than sucrose at pH 4 alone.
목차
Introduction
Materials and Methods
Results and Discussion
Acknowledgments
References
