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Enzymatic Synthesis of Banana Flavour (isoamyl acetate) by Bacillus Licheniformis S-86 Esterase

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dc.contributor.author Torres, S
dc.contributor.author Baigori, M D
dc.contributor.author Swathy, S L
dc.contributor.author Pandey, A
dc.contributor.author Castro, G R
dc.date.accessioned 2016-12-09T09:59:42Z
dc.date.available 2016-12-09T09:59:42Z
dc.date.issued 2009-05
dc.identifier.citation Food Research International, 42(4):454-460 en_US
dc.identifier.uri http://hdl.handle.net/123456789/2550
dc.description.abstract New 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.iso en en_US
dc.publisher Elsevier en_US
dc.subject Esterases en_US
dc.subject Bacillus licheniformis esterase en_US
dc.subject Characterization en_US
dc.subject Transesterification en_US
dc.subject Isoamyl acetate en_US
dc.title Enzymatic Synthesis of Banana Flavour (isoamyl acetate) by Bacillus Licheniformis S-86 Esterase en_US
dc.type Article en_US


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