Method for preoaration of purified propylhomoserin esterase
A technology of arginine ester and enzyme activity, which is applied in the field of preparation of biological drugs and can solve the problems of toxic substances and low purity of arginine esterase.
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[0012] Take 20 grams of Jiangsu-Zhejiang Agkistrodon venom freeze-dried powder, dissolve in 20ml of 0.05M Tris-HCl, pH7.8 buffer solution, centrifuge in a refrigerated centrifuge at 3000 rpm for 10 minutes, remove insoluble matter, and add the supernatant to DEAE cellulose DE-52 chromatographic column, 3×80cm, the chromatographic column needs to be equilibrated with Tris-HCl buffer first, the eluent is gradient eluted with a concentration of 0 to 0.5M containing NaCl, and the arginine esterase activity is collected Components (detected at a wavelength of 280nm by an ultraviolet spectrophotometer), the collected liquid was combined, concentrated by ultrafiltration with an ultrafiltration membrane with a molecular weight cut-off of more than 10,000, dialyzed to remove salt, and then separated by CM-Sepharose column chromatography. The size is 2×40cm; equilibrate with 0.05M sodium acetate buffer solution pH5.0, after adding the sample, carry out gradient elution with sodium acetat...
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