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

IR@CSIR-CFTRI

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Relation http://ir.cftri.com/13185/
http://dx.doi.org/10.1007/s12010-008-8414-x
 
Title Syntheses of Retinol Glycosides Using β-glucosidase
in SCCO2 Media.
 
Creator Charles, Rajachristu Einstein
Ponrasu, Thangavel
Udaya Sankar, K.
Divakar, S.
 
Subject 17 Vitamin Biochemistry
 
Description 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.
 
Date 2009
 
Type Article
PeerReviewed
 
Format pdf
 
Language en
 
Identifier http://ir.cftri.com/13185/1/Appl%20Biochem%20Biotechnol%20%282009%29%20159%20199%E2%80%93207.pdf
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