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Protease Immobilization on gamma-Fe_(2)O_(3)/Fe_(3)O_(4) Magnetic Nanoparticles for the Synthesis of Oligopeptides in Organic Solvents

机译:蛋白酶固定在γ-Fe_(2)O_(3)/ Fe_(3)O_(4)磁性纳米粒子上,用于有机溶剂中寡肽的合成

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摘要

The use of nanobiocatalysts, with the combination of nanotechnology and biotechnology, is considered as an exciting and rapidly emerging area. The use of iron oxide magnetic nanoparticles, as enzyme immobilization carriers, has drawn great attention because of their unique properties, such as controllable particle size, large surface area, modifiable surface, and easy recovery. In this study, various gamma-Fe_(2)O_(3)/Fe_(3)O_(4) magnetic nanoparticles with immobilized proteases were successfully prepared by three different immobilization strategies including A) direct binding, B) with thiophene as a linker, and C) with triazole as a linker. The oligopeptides syntheses catalyzed by these magnetic nanoparticles (MNPs) with immobilized proteases were systematically studied. Our results show that i) for magnetic nanoparticles immobilized alpha-chymotrypsin, both immobilization strategies A and B furnished good reusability for the Z-Tyr-Gly-Gly-OEt synthesis, the MNPs enzymes can be readily used at least five times without significant loss of its catalytic performance: ii) In the case of Z-Asp-Phe-OMe synthesis catalyzed by magnetic nanoparticles immobilized thermolysin, immobilization Strategy B provided the best recyclability: iii) For the immobilized papain, although Strategy A or B afforded an immobilized enzyme for the first cycle of Z-Ala-Leu-NHNHPh synthesis in good yield, their subsequent catalytic activity decreased rapidly. In general, the gamma-Fe_(2)O_(3) MNPs were better for use as an immobilization matrix, rather than the Fe_(3)O_(4) MNPs, owing to their smaller particle size and higher surface area.
机译:纳米生物催化剂的使用以及纳米技术和生物技术的结合,被认为是一个令人兴奋且迅速兴起的领域。氧化铁磁性纳米颗粒作为酶固定载体的使用,由于其独特的特性(如可控制的粒径,较大的表面积,可修饰的表面以及易于回收)而备受关注。在这项研究中,通过三种不同的固定化策略成功制备了各种具有固定蛋白酶的γ-Fe_(2)O_(3)/ Fe_(3)O_(4)磁性纳米粒子,包括A)直接结合,B)以噻吩为接头的固定化策略。和C),其中三唑为连接基。系统地研究了这些磁性纳米颗粒(MNP)与固定化蛋白酶催化的寡肽合成。我们的结果表明,i)对于磁性纳米颗粒固定化的α-胰凝乳蛋白酶,固定化策略A和B都为Z-Tyr-Gly-Gly-OEt合成提供了良好的可重用性,MNPs酶可轻松使用至少五次而不会造成重大损失的催化性能:ii)在固定有嗜热菌素的磁性纳米颗粒催化的Z-Asp-Phe-OMe合成中,固定化策略B提供了最佳的可回收性:iii)对于固定化的木瓜蛋​​白酶,尽管策略A或B提供了固定化酶Z-Ala-Leu-NHNHPh合成的第一个周期以高收率反应,其随后的催化活性迅速下降。通常,由于γ-Fe_(2)O_(3)MNPs的粒径较小且表面积较大,因此比Fe_(3)O_(4)MNPs更好地用作固定基质。

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