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首页> 外文期刊>Chemical engineering journal >Well-defined bioarchitecture for immobilization of chloroperoxidase on magnetic nanoparticles and its application in dye decolorization
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Well-defined bioarchitecture for immobilization of chloroperoxidase on magnetic nanoparticles and its application in dye decolorization

机译:定义明确的生物体系结构将氯过氧化物酶固定在磁性纳米颗粒上及其在染料脱色中的应用

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摘要

Molecular orientation of chloroperoxidase (CPO) on surface of Fe3O4 magnetic nanoparticles (MNPs) was achieved through layer-by-layer (LBL) controlled assembly by site specific interactions of avidin and bio-tin. Enzymatic oxidative decolorization of soluble aniline blue was employed to evaluate the catalytic performance of immobilized CPO (I-CPO). The decolorization efficiency of dye by I-CPO was higher than 90% within 10 min. Moreover, I-CPO displayed improved thermostability and kept higher activity in wider pH range and in the presence of high concentration of oxidant (H2O2) compared to that of free enzyme. When incubated at 70 °C for an hour, 42.35% of the activity of immobilized enzyme was reserved compared with that at 25 °C, whereas free CPO remained only 8.46%. The tolerance to H2O2 was improved from 2 mmol L~(-1) to 4 mmol L~(-1) and the suitable pH range become wider. The relative activities of I-CPO in the 20 times use maintained 62% of that in the first run. The enzymatic kinetic constants confirmed that the entrapping CPO into this well-defined architecture could reduce diffusional limitation of reac-tants and products.
机译:Fe3O4磁性纳米颗粒(MNPs)表面上的氯过氧化物酶(CPO)的分子取向是通过抗生物素蛋白和生物素的位点特异性相互作用通过逐层(LBL)控制的组装来实现的。可溶性苯胺蓝的酶氧化脱色用于评估固定化CPO(I-CPO)的催化性能。 I-CPO在10分钟内对染料的脱色效率高于90%。此外,与游离酶相比,I-CPO在更宽的pH范围内和高浓度氧化剂(H2O2)的存在下表现出更高的热稳定性,并保持较高的活性。在70°C下孵育一个小时,与25°C下相比,保留了42.35%的固定化酶活性,而游离CPO仅保留8.46%。对H2O2的耐受性从2 mmol L〜(-1)提高到4 mmol L〜(-1),合适的pH范围变宽。 I-CPO在20次使用中的相对活动保持了第一次运行时的62%。酶促动力学常数证实,将CPO包埋在这种定义明确的结构中可以减少反应物和产物的扩散限制。

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