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dc.contributor.authorTorres, S-
dc.contributor.authorBaigori, M D-
dc.contributor.authorSwathy, S L-
dc.contributor.authorPandey, A-
dc.contributor.authorCastro, G R-
dc.date.accessioned2016-12-09T09:59:42Z-
dc.date.available2016-12-09T09:59:42Z-
dc.date.issued2009-05-
dc.identifier.citationFood Research International, 42(4):454-460en_US
dc.identifier.urihttp://hdl.handle.net/123456789/2550-
dc.description.abstractNew carboxylesterase from organic-solvent-tolerant Bacillus licheniformis S-86 strain was characterized. The enzyme named as type II esterase showed an optimal activity in the temperature range 60–65 °C and pH 8.0. The enzyme was moderatly thermostable (half-life of 1 h at 50 °C), but remarkable stable at extremely alkaline pH, retaining 100% of its activity at pH 10.0–11.0. Furthermore, the esterase showed high stability in detergents (86% residual activity in 10% SDS), and also 0.1% ionic and non-ionic detergents are inducers of enzyme activity. PMSF, a serine protease inhibitor, did not show any effect on the activity. The immobilized type II esterase was able to synthesize isoamyl acetate from isoamyl alcohol and p-nitrophenyl acetate (acyl donor) in n-hexane. The resulting ester yield (42.8%), obtained at a low temperature (28 °C) and with a very low amount of enzyme (4.6 × 10−5 mg ml−1), indicates a high potential for type II esterase in isoamyl acetate synthesis for production purposes.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectEsterasesen_US
dc.subjectBacillus licheniformis esteraseen_US
dc.subjectCharacterizationen_US
dc.subjectTransesterificationen_US
dc.subjectIsoamyl acetateen_US
dc.titleEnzymatic Synthesis of Banana Flavour (isoamyl acetate) by Bacillus Licheniformis S-86 Esteraseen_US
dc.typeArticleen_US
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