Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4635
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dc.contributor.authorAmena S
dc.contributor.authorVishalakshi N
dc.contributor.authorPrabhakar M
dc.contributor.authorDayanand A
dc.contributor.authorLingappa K.
dc.date.accessioned2020-06-12T15:04:25Z-
dc.date.available2020-06-12T15:04:25Z-
dc.date.issued2010
dc.identifier.citationBrazilian Journal of Microbiology , Vol. 41 , 1 , p. 173 - 178en_US
dc.identifier.uri10.1590/S1517-83822010000100025
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4635-
dc.description.abstractL-asparaginase is an anti-neoplastic agent used in the lymphoblastic leukaemia chemotherapy. In the present study a novel strain, Streptomyces gulbargensis was explored for the production of extra-cellular L-asparaginase using groundnut cake extract. The optimum pH, temperature, inoculum size and agitation speed for enzyme production were pH 8.5, 40°C, 1×108spores/ml and 200 rev/min respectively. Maltose (0.5%) and L-asparagine (0.5%) proved to be the best carbon and nitrogen sources respectively. The enzyme was purified 82.12 fold and the apparent molecular weight of the enzyme was found to be 85 kDa. The optima pH and temperature for the enzyme were 9.0 and 40°C respectively. The enzyme was more stable at the alkaline pH than at the acidic one and it retained 55% of the activity at 80°C for 60 min.en_US
dc.publisherSociedade Brasileira de Microbiologia
dc.subjectGroundnut cake extract
dc.subjectL-asparaginase
dc.subjectOptimization
dc.subjectPurification
dc.subjectStreptomyces gulbargensis
dc.titleProduction, purification and characterization of L-asparaginase from Streptomyces gulbargensisen_US
dc.typeArticle
Appears in Collections:1. Journal Articles

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