Immobilization of Candida sp. lipase on resin D301.
- Author:
Yanhua WANG
1
;
Kai ZHU
;
Hui LIU
;
Pingfang HAN
;
Ping WEI
Author Information
1. Biotechnology and Pharmaceutical Engineering, Nanjing University of Technology, Nanjing 210009, China.
- Publication Type:Journal Article
- MeSH:
Candida;
enzymology;
Enzyme Stability;
Enzymes, Immobilized;
chemistry;
drug effects;
metabolism;
Ion Exchange Resins;
pharmacology;
Lipase;
chemistry;
metabolism
- From:
Chinese Journal of Biotechnology
2009;25(12):2036-2041
- CountryChina
- Language:Chinese
-
Abstract:
We immobilized Candida sp. lipase onto seven kinds of industrial adsorption and ion exchange resins. By determining the activity of each immobilized enzyme, the weakly basic anionic exchange resin of D301 showed the best results for the immobilization of Candida sp. lipase. Comparing the scanning electron micrographs of D301 with Novozym 435 (immobilized Candida antarctica lipase B from Novo Nordisk Corp.), we selected D301 as a carrier for the immobilization of Candida sp. lipase. And we pretreated the resin D301 with the bifunctional agent glutaraldehyde and crosslinked it with Candida sp. lipase. The optimal conditions for the immobilization of Candida sp. lipase were as follows: 8 mL of the amount of 5% glutaraldehyde solution, five hours of the time pretreated D301 with glutaraldehyde, 1.0 g/L the concentration of Candida sp. lipase used, pH of the phosphate buffered, 6.0 and 10 hours of time for immobilization, respectively. The activity of immobilized enzyme was over 35 U/mg and the efficiency of immobilization was around 3.5 Ul(mg x h).
