期刊
PROGRESS IN ENVIRONMENTAL SCIENCE AND ENGINEERING, PTS 1-4
卷 610-613, 期 -, 页码 203-209出版社
TRANS TECH PUBLICATIONS LTD
DOI: 10.4028/www.scientific.net/AMR.610-613.203
关键词
organophosphate-degrading enzyme; Expression; Purification; Characterization
OpdA is one of organic phosphorus degradation enzyme gene from Agrobacterium radiobacter that may be the most promising targets for the digestion of digestion. In this study, we describe for the cloning and expression in Escherichia coli (E. coli) of plasmid pET28b-opdA, followed by purification by NTA-Ni2+ agarose affinity chromatography. Protein expression and purification were evaluated by sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE).The Results showed that the optimal value of inoculum OD600 before induction, inducing time, final IPTG concentration and inducing temperature respectively were 0.5,5h,1 mmol/L,37 degrees C. We obtained the concentration of renatured protein was 18.312mg / L. The Km was 4.26 mu mol/L at 37 degrees C, and the maximum reaction velocity (Vmax) was 3.2669 mu mol/L . min.
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