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Comparative studies on the sugar esters synthesis catalysed by Candida antarctica and Candida rugosa lipases in hexane

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dc.contributor.author Tsitsimpikou, C en
dc.contributor.author Daflos, H en
dc.contributor.author Kolisis, FN en
dc.date.accessioned 2014-03-01T01:12:41Z
dc.date.available 2014-03-01T01:12:41Z
dc.date.issued 1997 en
dc.identifier.issn 1381-1177 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/12204
dc.subject Lipase en
dc.subject Sugar-fatty acid esters en
dc.subject Water activity en
dc.subject.classification Biochemistry & Molecular Biology en
dc.subject.classification Chemistry, Physical en
dc.subject.other Acylation en
dc.subject.other Bacteria en
dc.subject.other Enzyme immobilization en
dc.subject.other Esters en
dc.subject.other Fructose en
dc.subject.other Glucose en
dc.subject.other Organic solvents en
dc.subject.other Paraffins en
dc.subject.other Sugars en
dc.subject.other Lipases en
dc.subject.other Monosaccharides en
dc.subject.other Enzymes en
dc.subject.other arabinose en
dc.subject.other fructose en
dc.subject.other glucose en
dc.subject.other mannose en
dc.subject.other monosaccharide en
dc.subject.other triacylglycerol lipase en
dc.subject.other acylation en
dc.subject.other article en
dc.subject.other chemical structure en
dc.subject.other enzyme activity en
dc.subject.other nonhuman en
dc.subject.other structure analysis en
dc.subject.other temperature en
dc.title Comparative studies on the sugar esters synthesis catalysed by Candida antarctica and Candida rugosa lipases in hexane en
heal.type journalArticle en
heal.identifier.primary 10.1016/S1381-1177(97)89617-8 en
heal.identifier.secondary http://dx.doi.org/10.1016/S1381-1177(97)89617-8 en
heal.language English en
heal.publicationDate 1997 en
heal.abstract The regioselective acylation of monosaccharides, such as glucose, fructose, mannose and arabinose with lauric acid (C12) has been investigated in hexane using commercial Candida rugosa lipase (EC 3.1.1.3) and Candida antarctica (NOVO-ZYME) lipase immobilised on anionic resin. In order to overcome sugars insolubility in hexane, sugars were introduced in the reaction mixture preabsorbed on silica gel. The chemical structure of the products has been determined by 1H NMR analysis. The two enzymes tested seemed to prefer hexoses rather than pentoses as the sugar substrate. They exhibited different water activity optimums as well as different optimum sugar/acyl donor molar ratios. Water activity control throughout the reaction and temperature increase from 30 to 50°C enhanced sugar ester production using both lipases.The regioselective acylation of monosaccharides, such as glucose, fructose, mannose and arabinose with lauric acid (C12) has been investigated in hexane using commercial Candida rugosa lipase (EC 3.1.1.3) and Candida antarctica (NOVOZYME) lipase immobilised on anionic resin. In order to overcome sugars insolubility in hexane, sugars were introduced in the reaction mixture preabsorbed on silica gel. The chemical structure of the products has been determined by H NMR analysis. The two enzymes tested seemed to prefer hexoses rather than pentoses as the sugar substrate. They exhibited different water activity optimums as well as different optimum sugar/acyl donor molar ratios. Water activity control throughout the reaction and temperature increase from 30 to 50°C enhanced sugar ester production using both lipases. en
heal.publisher Elsevier Sci B.V., Amsterdam, Netherlands en
heal.journalName Journal of Molecular Catalysis - B Enzymatic en
dc.identifier.doi 10.1016/S1381-1177(97)89617-8 en
dc.identifier.isi ISI:A1997XF11500024 en
dc.identifier.volume 3 en
dc.identifier.issue 1-4 en
dc.identifier.spage 189 en
dc.identifier.epage 192 en


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