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Please use this identifier to cite or link to this item: http://hdl.handle.net/2080/1065

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contributor.authorTripathi, N K-
contributor.authorShrivastva, A-
contributor.authorBiswal, K C-
contributor.authorP V, Lakshmana Rao-
date.accessioned2009-11-04T07:57:04Z-
date.available2009-11-04T07:57:04Z-
date.issued2009-09-01-
identifier.citationIndustrial Biotechnology. September 2009, Volume 5 No 3, pages 179-183en
identifier.urihttp://dx.doi.org/10.1089/ind.2009.3.179.-
identifier.urihttp://hdl.handle.net/2080/1065-
description.abstractEnhanced production of recombinant dengue multi-epitope protein in Escherichia coli was achieved by optimization of culture medium. Complex media (Luria Bertani broth, Terrific broth, Super broth, M9 minimal media, five times Luria Bertani broth, semi-defined medium enriched with tryptone and yeast extract, and semi-defined medium enriched with glucose) were evaluated for production of recombinant dengue multi-epitope protein in shake flasks. The recombinant protein was further produced by fed-batch fermentation using 5 L bioreactor. Cells were grown in optimized semi-defined medium, and feeding was carried out with 5X medium and glycerol. When growth reached 14.35 g/L of dry cell weight, culture was induced with 0.5 mM IPTG and further grown for 4 h to reach 18.37 g/L dry cell weight. The recombinant dengue multi-epitope protein was purified from inclusion bodies under denaturing conditions using metal affinity chromatography, which yielded 96.43 mg/L of protein. The purified protein was found to be reactive with dengue-infected human serum samplesen
format.extent1355965 bytes-
format.mimetypeapplication/pdf-
language.isoen-
publisherMary Ann Lieberten
subjectEscherichia coli,en
subjectfed-batch cultivation,en
subjectrecombinant dengue proteinen
titleOptimization of Culture Medium for Production of Recombinant Dengue Protein in Escherichia Colien
typeArticleen
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