Carbodiimide for Covalent α-Amylase Immobilization onto Magnetic Nanoparticles

淀粉酶 碳二亚胺 固定化酶 共价键 纳米颗粒 傅里叶变换红外光谱 磁性纳米粒子 材料科学 核化学 化学工程 化学 色谱法 有机化学 高分子化学 纳米技术 工程类
作者
Zeinab Mortazavi Milani,Razieh Jalal,Elaheh K. Goharshadi
出处
期刊:International Journal of Nanoscience [World Scientific]
卷期号:16 (05n06): 1750015-1750015 被引量:18
标识
DOI:10.1142/s0219581x17500156
摘要

Covalent cross-linking of enzymes to magnetite (Fe 3 O 4 ) nanoparticles (MNPs) is one of the useful enzyme immobilization methods which provides repeated use of the catalyst, facilitates enzyme separation from the reaction mixture, and sometimes improves biocatalysts stability. The aim of this study was to immobilize [Formula: see text]-amylase onto MNPs via covalent attachment using carbodiimide (CDI) molecules. MNPs were synthesized by the co-precipitation method. The size and the structure of the particles were characterized by X-ray diffraction and transmission electron microscopy. The effects of different operational conditions of direct [Formula: see text]-amylase binding on MNPs in the presence of CDI were investigated by using the shaking method. Fourier transform infrared spectroscopy was used to confirm the success of immobilization. The optimum conditions and catalytic properties of immobilized [Formula: see text]-amylase were also evaluated. The efficiency of immobilization and the residual activity of the immobilized [Formula: see text]-amylase were dependent on the mass ratio of MNPs: CDI: [Formula: see text]-amylase and the immobilization temperature. The optimum pH for the free and immobilized amylase was 6. The free and immobilized [Formula: see text]-amylase showed maximum activity at 20[Formula: see text]C and 35[Formula: see text]C, respectively. The immobilized [Formula: see text]-amylase was more thermostable than the free one. The retained activity for free [Formula: see text]-amylase after 19 storage days was 57.7% whereas it was 100% for the immobilized [Formula: see text]-amylase. In repeated batch experiments, the immobilized [Formula: see text]-amylase retained a residual activity of 45% after 11 repeated uses. The [Formula: see text] and [Formula: see text] values for the immobilized enzyme were larger than those of the free enzyme. The immobilization of [Formula: see text]-amylase on MNPs using CDI improves its stability and reusability.

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