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Syntheses of Retinol Glycosides Using β-glucosidase in SCCO2 Media.

Charles, Rajachristu Einstein and Ponrasu, Thangavel and Udaya Sankar, K. and Divakar, S. (2009) Syntheses of Retinol Glycosides Using β-glucosidase in SCCO2 Media. Applied Biochemistry and Biotechnology, 159. pp. 199-207. ISSN 0273-2289

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Abstract

β-Glucosidase isolated from sweet almond catalyzed syntheses of water soluble retinol glycosides were carried out in SCCO2 media with carbohydrates—D-glucose 2, Dgalactose 3, D-mannose 4, D-fructose 5, and D-sorbitol 6. Retinol glycosides yields were in the 9–34% range. Reaction with D-fructose 5 gave a highest yield of 34%. Excellent regioselectivity was observed with D-mannose 4 and D-sorbitol 6 which gave exclusively C1β-mannoside and C1-D-sorbitolide.

Item Type: Article
Uncontrolled Keywords: β-glucosidase . Regioselectivity . Retinol . Retinol glycoside . Supercritical carbon dioxide media (SCCO2) . Enzymatic catalysis
Subjects: 500 Natural Sciences and Mathematics > 07 Life Sciences > 03 Biochemistry & Molecular Biology > 17 Vitamin Biochemistry
Divisions: Fermentation Technology and Bioengineering
Food Engineering
Depositing User: Food Sci. & Technol. Information Services
Date Deposited: 29 Nov 2017 10:59
Last Modified: 29 Nov 2017 10:59
URI: http://ir.cftri.com/id/eprint/13185

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