DFT study on classical Koshland retention mechanism of Linamarin hydrolysis

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dc.contributor.authorDinuka,D. L. S
dc.contributor.authorRatnaweera,C. N
dc.date.accessioned2025-02-23T10:20:01Z
dc.date.available2025-02-23T10:20:01Z
dc.date.issued2019-05
dc.descriptionTechnical Sessions : A - 28 Page 35
dc.description.abstractT he hydrolysis of glucosidic linkage catalyzed by every carbohydrate-hydrolase is a reaction in which the product retains (α→α or β→β) or inverts (α→β or β→α) the anomeric configuration of the substrate. By releasing α-glucose and β-glucose, respectively, from the common substrates having α or β -glucosidic linkages, α-glucosidase and β-glucosidase are essentially distinguished.
dc.identifier.urihttps://dr.ichemc.ac.lk/handle/123456789/310
dc.language.isoen
dc.publisherInstitute of Chemistry Ceylon
dc.relation.ispartofseries36; 2
dc.subjectDensity functional theory
dc.subjectCyanogenic glycoside
dc.subjectOxocarbenium ion
dc.subjectretaining glycoside-hydrolase
dc.titleDFT study on classical Koshland retention mechanism of Linamarin hydrolysis
dc.typeArticle

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