| 저자(한글) |
Ling, Xiao-Min,Wang, Xiang-Yu,Ma, Ping,Yang, Yi,Qin, Jie-Mei,Zhang, Xue-Jun,Zhang, Ye-Wang |
| 초록 |
Penicillin G acylase (PGA) was immobilized on magnetic Fe 3 O 4 @chitosan nanoparticles through the Schiff base reaction. The immobilization conditions were optimized as follows: enzyme port 8.8 mg g, pH 6.0, time 40 min, and temperature 25 #8451;. Under these conditions, a high immobilization efficiency of 75% and a protein loading of 6.2 mg/g-support were obtained. Broader working pH and higher thermostability were achieved by the immobilization. In addition, the immobilized PGA retained 75% initial activity after ten cycles. Kinetic parameters V max and K m of the free and immobilized PGAs were determined as 0.113 mmol/min/mg-protein and 0.059 mmol/min/mg-protein, and 0.68 mM and 1.19 mM, respectively. Synthesis of amoxicillin with the immobilized PGA was carried out in 40% ethylene glycol at 25 #8451; and a conversion of 72% was obtained. These results showed that the immobilization of PGA onto magnetic chitosan nanoparticles is an efficient and simple way for preparation of stable PGA. |
