Yang Chengli, Xing Jianmin, Guan Yueping, Liu Huizhou
Laboratory of Separation Science and Engineering, State Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese Academy of Sciences, P.O. Box 353, Beijing 100080, People's Republic of China.
Appl Microbiol Biotechnol. 2006 Sep;72(3):616-22. doi: 10.1007/s00253-006-0484-5. Epub 2006 May 31.
An effective method for purification of nattokinase from fermentation broth using magnetic poly(methyl methacrylate) (PMMA) beads immobilized with p-aminobenzamidine was proposed in this study. Firstly, magnetic PMMA beads with a narrow size distribution were prepared by spraying suspension polymerization. Then, they were highly functionalized via transesterification reaction with polyethylene glycol. The surface hydroxyl-modified magnetic beads obtained were further modified with chloroethylamine to transfer the surface amino-modified magnetic functional beads. The morphology and surface functionality of the magnetic beads were examined by scanning electron microscopy and Fourier transform infrared. An affinity ligand, p-aminobenzamidine was covalently immobilized to the amino-modified magnetic beads by the glutaraldehyde method for nattokinase purification directly from the fermentation broth. The purification factor and the recovery of the enzyme activity were found to be 8.7 and 85%, respectively. The purification of nattokinase from fermentation broth by magnetic beads only took 40 min, which shows a very fast purification of nattokinase compared to traditional purification methods.
本研究提出了一种使用固定有对氨基苯甲脒的磁性聚甲基丙烯酸甲酯(PMMA)微珠从发酵液中纯化纳豆激酶的有效方法。首先,通过喷雾悬浮聚合制备了尺寸分布狭窄的磁性PMMA微珠。然后,通过与聚乙二醇的酯交换反应对其进行高度功能化。将得到的表面羟基改性磁性微珠进一步用氯乙胺改性,以得到表面氨基改性的磁性功能微珠。通过扫描电子显微镜和傅里叶变换红外光谱对磁性微珠的形态和表面功能进行了检测。通过戊二醛法将亲和配体对氨基苯甲脒共价固定在氨基改性的磁性微珠上,用于直接从发酵液中纯化纳豆激酶。发现纯化因子和酶活性回收率分别为8.7和85%。用磁性微珠从发酵液中纯化纳豆激酶仅需40分钟,与传统纯化方法相比,这显示出纳豆激酶的纯化速度非常快。