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Synthesis of hybrid Fe_3O_4-silica-NiO superstructures and their application as magnetically separable high-performance biocatalysts

机译:杂化Fe_3O_4-二氧化硅-NiO超结构的合成及其在磁分离高性能生物催化剂中的应用

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摘要

The assembly of NiO nanoparticles at the surface of magnetic silica resulted in a hybrid superstructure which has utility as a carrier for a magnetically separable biocatalyst system.rnOver recent years, nano-sized particles have emerged as excellent supports for immobilizing biocatalysts, such as enzymes. Nanoparticles can support the maximum surface area available to immobilize enzymes with minimal steric hindrance to reactants for accessing their active sites, leading to high activity as free enzymes. Furthermore, magnetic nanoparticles can be separated facilely from the reaction solution by applying an external magnet. This can allow recycling of the immobilized enzymes for the next reaction, which can significantly reduce the cost in terms of large scale applications of expensive enzymes. In most previous approaches, immobilization was achieved though covalent bonding between the enzymes and nanoparticle surface. This may result in a loss of activity because the active site might be hidden or restricted from assuming the conformation needed to initiate catalysis. A method of immobilizing biomolecules on nanoparticles whilst retaining their biological activity is of immense interest. Recently, the concept of histidine-tagged (His-tagged) protein attachment to a metal terminated nitrilotri-acetate group has been demonstrated to efficiently immobilize enzymes on nanoparticles.
机译:NiO纳米颗粒在磁性二氧化硅表面的组装形成了一种杂化的上层结构,该杂化的上层结构可用作可磁分离的生物催化剂体系的载体。近年来,纳米级颗粒已成为固定化生物催化剂(如酶)的出色载体。纳米颗粒可以支持最大表面积,以最小限度的空间障碍将酶固定在反应物上,以使其进入活性位点,从而使游离酶具有很高的活性。此外,可以通过施加外部磁体容易地将磁性纳米颗粒与反应溶液分离。这可以使固定化的酶再循环用于下一步反应,就大规模应用昂贵的酶而言,这可以显着降低成本。在大多数以前的方法中,固定化是通过酶和纳米颗粒表面之间的共价键实现的。这可能导致活性丧失,因为可能隐藏或限制了活性位点,使其无法承担启动催化作用所需的构象。将生物分子固定在纳米颗粒上同时保持其生物活性的方法引起了极大的兴趣。最近,已证明组氨酸标记(His标记)蛋白质附着在金属末端次氮基三乙酸酯基团上的概念可以有效地将酶固定在纳米颗粒上。

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  • 来源
    《Chemical Communications》 |2009年第25期|3780-3782|共3页
  • 作者单位

    Department of Applied Chemistry, College of Applied Sciences, Kyung Hee University, Gyeonggi-do 449-701, Korea;

    Department of Food Science and Biotechnology, Kyungsung University, Busan 608-736, Korea;

    Department of Food Science and Biotechnology, Kyungsung University, Busan 608-736, Korea;

    Department of Chemical Engineering, College of Engineering, Kyung Hee University, Gyeonggi-do 449-701, Korea;

    Department of Applied Chemistry, College of Applied Sciences, Kyung Hee University, Gyeonggi-do 449-701, Korea;

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