Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/1729
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dc.contributor.authorElyas, K K-
dc.contributor.authorMathew, A-
dc.contributor.authorRajeev K Sukumaran-
dc.contributor.authorAli, P P M-
dc.contributor.authorSapna, K-
dc.contributor.authorRamesh Kumar, S-
dc.contributor.authorRekha Mol, K R-
dc.date.accessioned2015-01-08T05:46:44Z-
dc.date.available2015-01-08T05:46:44Z-
dc.date.issued2010-
dc.identifier.citationNew Biotechnology 27(4):347-351.SI;30 Sep 2010en_US
dc.identifier.issn1871-6784-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/1729-
dc.description.abstractAspergillus strain SA 58, showing considerable beta glucosidase production was selected as the potential strain. The fungus showed enzyme production in both acidic and alkaline pH. A temperature of 35 degrees C was found to be optimum for enzyme production. Maximum enzyme production was seen when pectin was used as the carbon source (80 U/ml). In solid-state fermentation, an enzyme production of 6200 U/g Initial Dry Substrate was noted. The strain produced two extra cellular enzymes and two intra cellular enzymes. For both the extra cellular enzymes (BGL A and BGL B), 60 degrees C was found to be optimum temperature for activity. BGL A showed an optimum pH of 4.0 while BGL B showed an optimum pH of 3.0 for activity. Both the enzymes showed a second peak of activity at pH 9.0. Both BGL A and BGL B showed high thermal stabilities with residual activities of 86% and 85% even after 6 h of incubation at 50 degrees C.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectSolid-state fermentationen_US
dc.subjectGlucose-toleranten_US
dc.subjectTrichoderma-reeseien_US
dc.titleProduction optimization and properties of beta glucosidases from a marine fungus Aspergillus-SA 58en_US
dc.typeArticleen_US
Appears in Collections:2010

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