高等学校化学学报

高等学校化学学报

• 研究论文 • 上一篇    下一篇

用于α-胰凝乳蛋白酶固定化的氨基超顺磁纳米凝胶的光化学合成与表征

洪军, 徐冬梅, 孙汉文, 宫培军, 董黎, 姚思德   

  1. 中国科学院上海应用物理研究所, 上海 201800
  • 收稿日期:2006-06-04 修回日期:1900-01-01 出版日期:2007-01-10 发布日期:2007-01-10
  • 通讯作者: 姚思德

Photochemical Synthesis and Characterization of Amine-functionalized Superparamagnetic Nanogel for α-Chymotrypsin Immobilization

HONG Jun, XU Dong-Mei, SUN Han-Wen, GONG Pei-Jun, DONG Li, YAO Si-De   

  1. Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai 201800, China
  • Received:2006-06-04 Revised:1900-01-01 Online:2007-01-10 Published:2007-01-10
  • Contact: YAO Si-De

PDF (PC)

摘要： 通过霍夫曼降解光化学原位聚合制备的聚丙烯酰胺包覆的Fe3O4纳米粒子得到了氨基化磁性纳米凝胶, 用缩合剂1-乙基-3-(3-二甲胺)碳二亚胺成功地将α-胰凝乳蛋白酶固定到氨基化磁性纳米凝胶上, 并采用光子相关光谱、傅里叶变换红外光谱、透射电子显微镜、X射线粉末衍射和热重-示差扫描量热联用等多种手段对其进行了表征. 固定化了的α-胰凝乳蛋白酶平均粒径约为31 nm; 热重法测得每克凝胶上的载酶量为69 mg, BCA 法测得每克凝胶上的载酶量为61 mg; 酶的固定化和氙灯辐照并未改变Fe3O4的晶形结构; 固定化酶比活力为0.93 U/(mg·min), 为自由酶活力的59.3%; 磁含量高达88%, 具有优异的磁响应性能, 可应用于诸多生物医药领域的快速检测、分离及酶的再生利用.

关键词: 光化学原位聚合, 固定化酶, 超顺磁性Fe3O4, α-胰凝乳蛋白酶

Abstract: In this paper, amine-functionalized superparamagnetic nanogel was obtained by Hoffman degradation of the PAM-coated Fe3O4 nanoparticles prepared by photochemical in situ polymerization. α-Chymotrypsin was successfully bound to the magnetic nanogel with amino groups in the presence of 1-ethyl-3-(3-dimethylaminepropyl) carbodiimide(EDC). The immobilized enzyme was characterized by using photo correlation spectroscopy(PCS), transmission electron microscopy(TEM), X-ray diffraction(XRD) analysis, thermogravimetric-differential scanning calorimetry(TG-DSC) and Fourier transform infrared spectroscopy. Mean particle size of the immobilized enzyme was measured to be 31 nm by PCS; the binding capacity was 69 mg enzyme/g nanogel determined by TG analysis, 61 mg enzyme /g nanogel determined by standard BCA. The crystalline structure of Fe3O4 was affected by xenon lamp irradiation and enzyme immobilization. Magnetic content of the immobilized enzyme was as high as 88%. Specific activity of the immobilized α-chymotrypsin was 0.93 U/(min·mg), 59.3% of free form. It can be expected that the immobilized α-chymotrypsin has a potential in the fast detection and separation, as well as the reuse of immobilized enzymes.

Key words: Photochemical in situ polymerization, Immobilized enzyme, Superparamagnetic Fe3O4, α-Chymotrypsin

中图分类号: 

TrendMD: