Please use this identifier to cite or link to this item: https://idr.l2.nitk.ac.in/jspui/handle/123456789/11491
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dc.contributor.authorAithal, M.
dc.contributor.authorBelur, P.D.
dc.date.accessioned2020-03-31T08:31:31Z-
dc.date.available2020-03-31T08:31:31Z-
dc.date.issued2013
dc.identifier.citationPreparative Biochemistry and Biotechnology, 2013, Vol.43, 5, pp.445-455en_US
dc.identifier.urihttp://idr.nitk.ac.in/jspui/handle/123456789/11491-
dc.description.abstractEnzymatic synthesis of propyl gallate in organic solvent was studied using cell-associated tannase (EC 3.1.1.20) of Bacillus massiliensis. Lyophilized biomass showing tannase activity was used as the biocatalyst. The effects of solvent, surfactant treatment, and bioimprinting on the propyl gallate synthesis were studied and subsequently optimized. Among various solvents, benzene followed by hexane was found to be the most favorable. Treatment of the biocatalyst with Triton X-100 at a lower concentration (0.2% w/v), before lyophilization, increased the propyl gallate yield by 24.5% compared to the untreated biocatalyst. The biocatalyst was imprinted with various concentrations of gallic acid and tannic acid. Biocatalyst imprinted with tannic acid showed 50% enhancement in the propyl gallate yield compared to the non-imprinted biocatalyst. 2013 Taylor & Francis Group, LLC.en_US
dc.titleEnhancement of propyl gallate yield in nonaqueous medium using novel cell-associated tannase of bacillus massiliensisen_US
dc.typeArticleen_US
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