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首页> 外文期刊>Journal of nanoscience and nanotechnology >Fabrication of Gold Nanoparticle Assembled Polyurethane Microsphere Template in Trypsin Immobilization
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Fabrication of Gold Nanoparticle Assembled Polyurethane Microsphere Template in Trypsin Immobilization

机译:胰蛋白酶固定化金纳米粒子组装聚氨酯微球模板的制备

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摘要

The separation, reusability and high catalytic activity of bioconjugate remain challenging task in proteins bound gold nanoparticles. A facile synthetic route for the fabrication of gold nanoparticle assembled polyurethane microsphere template and immobilization of trypsin on gold/polyurethane surface to form trypsin-nanogold-polyurethane bioconjugate was developed. The bioconjugate was characterized by X-ray diffraction, Field emission scanning electron microscopy, Transmission electron microscopy, UV-visible, Fourier transform infrared, Fluorescence and Circular dichroism spectroscopy. The catalytic studies confirmed retention of ~40% of its original activity even after eight consecutive reaction cycles. The bioconjugate is also very effective for its separation from the reaction medium and exhibited significant enhanced stability over a wide range of pH and temperature compared to free trypsin. These findings clearly demonstrate that trypsin immobilized gold nanoparticle assembled polyurethane microsphere acts as an excellent recyclable biocatalyst with enzyme-specific biocompatibility.
机译:生物结合物的分离,可重复使用性和高催化活性仍然是蛋白质结合的金纳米颗粒中具有挑战性的任务。开发了一种简便的合成途径,用于制备金纳米颗粒组装的聚氨酯微球模板,并将胰蛋白酶固定在金/聚氨酯表面上,以形成胰蛋白酶-纳米金-聚氨酯生物共轭物。通过X射线衍射,场发射扫描电子显微镜,透射电子显微镜,紫外可见光,傅立叶变换红外光谱,荧光和圆二色光谱对生物共轭物进行表征。催化研究证实,即使经过八个连续的反应循环,其原始活性仍保持约40%。与游离胰蛋白酶相比,该生物缀合物对于从反应介质中分离也是非常有效的,并且在宽的pH和温度范围内表现出显着增强的稳定性。这些发现清楚地表明,胰蛋白酶固定化的金纳米颗粒组装的聚氨酯微球是具有酶特异性生物相容性的优良的可回收生物催化剂。

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