Syntheses of Retinol Glycosides Using β-glucosidase in SCCO2 Media.
IR@CFTRI: CSIR-Central Food Technological Research Institute, Mysore
View Archive Info| Field | Value | |
| Relation |
http://ir.cftri.com/13185/
http://dx.doi.org/10.1007/s12010-008-8414-x |
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| Title |
Syntheses of Retinol Glycosides Using β-glucosidase
in SCCO2 Media.
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| Creator |
Charles, Rajachristu Einstein
Ponrasu, Thangavel Udaya Sankar, K. Divakar, S. |
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| Subject |
17 Vitamin Biochemistry
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| 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.
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| Date |
2009
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| Type |
Article
PeerReviewed |
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| Format |
pdf
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| Language |
en
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| 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 |
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