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Optimized refolding and characterization of S-peroxidase (CWPO_C of Populus alba) expressed in E. coli.

Protein Expr Purif.. 2011-12; 
Le Thanh Mai Pham, Su Jin Kim, Bong Keun Song, Yong Hwan Kim. Department of Chemical Engineering, Kwangwoon University, 447-1 Wolgye-Dong, Nowon-Gu, Seoul 139-701, Republic of Korea.
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摘要

Cationic cell wall peroxidase (CWPO_C) from poplar tree (Populus alba L) was heterologously expressed in Escherichia coli as an inclusion body. The insoluble inclusion body was solubilized and reactivated via a refolding procedure. The condition for this procedure was optimized by varying the refolding pH, and the concentrations of the oxidizing agent (GSSG), denaturing agent (GndCl), and hemin, respectively. The optimal conditions for refolding CWPO_C were 100 mM Tris-HCl at pH 8.5, 0.6mM GSSG, 5 µM hemin, 0.6 M GndCl and 5 mM CaCl?. The fact that the absorbance spectrum was identical to that of wild CWPO_C from poplar tree suggests that the protein folding, heme insertion and iron coordination were corr... More

关键词

Populus alba L; S peroxidase; Sinapyl alcohol; Refolding; Cell wall peroxidase