Liu Ruijiang, Chen Dan, Fu Hongxia, Lv Pingxue, Zhang Die, He Yunjie
J Nanosci Nanotechnol. 2017 Feb;17(2):893-99. doi: 10.1166/jnn.2017.12694.
A facile sol combustion and gel calcination process has been reported for the preparation of core– shell magnetic Zn0.5Fe₂O₄@SiOnanocomposites. The morphology, chemical composition, structure and magnetic property of as-prepared nanocomposites were investigated by XRD, VSM, BET, SEM, and TEM, and the magnetic Ni0.5Zn0.5Fe₂O₄@SiO₂ nanocomposites were characterized with average size of about 25 nm, saturation magnetization of 90.8 Am²/kg and the specific surface area of 67.1 m2/g. The surface of Ni0.5Zn0.5Fe₂O₄@SiO₂ nanocomposites was functionalized with glutaraldehyde to form the aldehyde-functionalized magnetic Ni0.5Zn0.5Fe₂O4@SiO₂ nanocomposites, and penicillin G acylase (PGA) was successfully immobilized onto them. And the immobilized PGA exhibited high effective activity, good stability of enzyme catalyst and good reusability, and could retain 63.5% of initial activity after 12 consecutive operations. The kinetic parameters were determined, and the value of K m for the immobilized PGA (161.7 mmol/L) is higher than that of the free PGA (3.5 mmol/L), while v max (1.626 mmol/min) is also larger than that of the free PGA (0.838 mmol/min), which revealed that the immobilization of PGA onto Ni0.5Zn0.5Fe₂O₄@SiO₂ nanocomposites was an efficient and simple way for preparation of stable PGA.
据报道,一种简便的溶胶燃烧和凝胶煅烧工艺可用于制备核壳磁性Zn0.5Fe₂O₄@SiO₂纳米复合材料。通过XRD、VSM、BET、SEM和TEM对所制备纳米复合材料的形貌、化学成分、结构和磁性进行了研究,所制备的磁性Ni0.5Zn0.5Fe₂O₄@SiO₂纳米复合材料的平均尺寸约为25 nm,饱和磁化强度为90.8 Am²/kg,比表面积为67.1 m²/g。用戊二醛对Ni0.5Zn0.5Fe₂O₄@SiO₂纳米复合材料的表面进行功能化处理,形成醛基功能化磁性Ni0.5Zn0.5Fe₂O₄@SiO₂纳米复合材料,并成功地将青霉素G酰化酶(PGA)固定在其上。固定化的PGA表现出高效活性、良好的酶催化剂稳定性和良好的可重复使用性,连续操作12次后可保留63.5%的初始活性。测定了动力学参数,固定化PGA的Km值(161.7 mmol/L)高于游离PGA的Km值(3.5 mmol/L),而vmax(1.626 mmol/min)也大于游离PGA的vmax(0.838 mmol/min),这表明将PGA固定在Ni0.5Zn0.5Fe₂O₄@SiO₂纳米复合材料上是制备稳定PGA的一种有效且简便的方法。