Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/13314
Title: Secretion of cyclodextrin glucanotransferase in E. coli using Bacillus subtilis lipase signal peptide and optimization of culture medium
Authors: Ayadi-Zouari, Dorra
Kammoun, Radhouane
Jemli, Sonia
Chouayekh, Hichem
Bejar, Samir
Keywords: E. coli
Optimization
Recombinant CGTase
Response surface methodology
Secretion
Signal peptide
Issue Date: Jan-2012
Publisher: NISCAIR-CSIR, India
Abstract: The cyclodextrin glycosyltransferase (CGTase) of Paenibacillus pabuli US132 was fused to the secretive lipase signal peptide of B. subtilis. This leads to an efficient secretion of the recombinant enzyme into the culture medium of E. coli as an active and soluble form contrasting with the native construction leading to a periplasmic production. In order to enhance the yield of CGTase production, an experimental design methodology was applied for the optimization of the culture composition. Hence, the media components were submitted to preliminary screening using a Plakett-Burman design. The concentrations of the major operating ones were then optimized to enhance the secretion of CGTase using response surface methodology. The findings revealed that concentrations of 0.5% potato starch, 3% yeast extract, 3% tryptone, 1.5% casein hydrolysate, 0.5% NaCl, 0.2% KH2PO4, and 0.02% MgSO4 were the optimal conditions for CGTase production. The experimental value (9.43 U/ml) obtained for CGTase activity was very close to the predicted value (9.27 U/ml).
Description: 72-79
URI: http://hdl.handle.net/123456789/13314
ISSN: 0975-1009 (Online); 0019-5189 (Print)
Appears in Collections:IJEB Vol.50(01) [January 2012]

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