Enzymatic synthesis of alkyl glucosides using Leuconostoc mesenteroides dextransucrase.

Abstract:

:Alkyl glucosides were synthesized by the reaction of Leuconostoc mesenteroides dextransucrase with sucrose and various alcohols. Alkyl alpha-D-glucosides were obtained with a yield of 30% (mol/mol) with primary alcohols, but secondary alcohols or tertiary alcohols gave yields below 5%. The optimal yield was 50% using 1-butyl alpha-D-glucoside with 0.9 M 1-butanol. The acceptor products of methanol or ethanol were confirmed as methyl alpha-D-glucopyranoside and ethyl alpha-D: -glucopyranoside via MALDI-TOF MS and NMR analysis. Thus, methyl or ethyl alpha-D-glucoside constituted half the emulsification activities of Triton X-100 as commercially available surfactants.

journal_name

Biotechnol Lett

journal_title

Biotechnology letters

authors

Kim YM,Kim BH,Ahn JS,Kim GE,Jin SD,Nguyen TH,Kim D

doi

10.1007/s10529-009-0015-4

subject

Has Abstract

pub_date

2009-09-01 00:00:00

pages

1433-8

issue

9

eissn

0141-5492

issn

1573-6776

journal_volume

31

pub_type

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