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Dual effect of benzyl alcohol on α-glucosidase activity: efficient substrate for high yield transglucosylation and non-competitive inhibitor of its hydrolytic activity
- Source :
- Carbohydrate Research
- Publication Year :
- 2013
-
Abstract
- Benzyl alcohol, a potent anesthetic and bacteriostatic, can be efficiently glucosylated by alpha-glucosidase from Saccharomyces cerevisiae to produce benzyl alcohol alpha-glucoside with a 75% yield. However, while studying the transglucosylation reaction conditions, it was found out that benzyl alcohol is a non-competitive inhibitor of alpha-glucosidase's hydrolytic activity (K-i = 18 mM, toward maltose). Due to its interesting ability to be glycosylated by the enzyme and to inhibit its hydrolytic activity, we proposed a plausible mechanism for the phenolic alpha-glucosydase inhibitor's binding, since the mechanism of inhibition has not yet been elucidated. (C) 2013 Elsevier Ltd. All rights reserved.
- Subjects :
- Glycosylation
Stereochemistry
Saccharomyces cerevisiae
Biochemistry
Analytical Chemistry
Substrate Specificity
chemistry.chemical_compound
Hydrolysis
Non-competitive inhibition
Benzyl alcohol
Glycoside Hydrolase Inhibitors
alpha-Glucosidase inhibition
Maltose
chemistry.chemical_classification
Primary hydrolysis
Organic Chemistry
Temperature
Substrate (chemistry)
alpha-Glucosidases
General Medicine
Enzyme
chemistry
Transglucosylation
Yield (chemistry)
Benzyl Alcohol
Protein Binding
Subjects
Details
- ISSN :
- 1873426X
- Volume :
- 387
- Database :
- OpenAIRE
- Journal :
- Carbohydrate research
- Accession number :
- edsair.doi.dedup.....931fbb1baa5dc68b8e73612e069dd301