| Literature DB >> 26869599 |
Xiao-Min Ling1, Xiang-Yu Wang1, Ping Ma1, Yi Yang1, Jie-Mei Qin1, Xue-Jun Zhang2, Ye-Wang Zhang1,2.
Abstract
Penicillin G acylase (PGA) was immobilized on magnetic Fe3O4@chitosan nanoparticles through the Schiff base reaction. The immobilization conditions were optimized as follows: enzyme/support 8.8 mg/g, pH 6.0, time 40 min, and temperature 25°C. 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 Vmax and Km of the free and immobilized PGAs were determined as 0.91 mmol/min and 0.53 mmol/min, 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°C 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.Entities:
Keywords: Amoxicillin; Chitosan; Immobilization; Magnetic nanoparticles; penicillin G acylase
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Year: 2016 PMID: 26869599 DOI: 10.4014/jmb.1511.11052
Source DB: PubMed Journal: J Microbiol Biotechnol ISSN: 1017-7825 Impact factor: 2.351