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首页> 外文期刊>RSC Advances >Evaluating effective factors on the activity and loading of immobilized alpha-amylase onto magnetic nanoparticles using a response surface-desirability approach
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Evaluating effective factors on the activity and loading of immobilized alpha-amylase onto magnetic nanoparticles using a response surface-desirability approach

机译:使用响应表面期望方法评估对磁性纳米粒子的活性和加载活性和加载的有效因素

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摘要

The effects of different operational conditions of alpha-amylase covalent immobilization on magnetic nanoparticles (MNPs), such as initial enzyme concentration, glutaraldehyde (GA) concentration, pH, and ionic strength were investigated using a central composite design (CCD). Moreover, two responses, the biocatalyst activity and amount of immobilized enzyme were simultaneously studied using Derringer's desirability function. The optimum amount and activity of immobilized enzyme were determined to be 24.83% and 556.41 mg g(MNP)(-1) at an initial enzyme concentration of 999.86 ppm, solution pH of 4.6, GA concentration of 0.59%, ionic strength of 99.99 mM and a process time of 4 h. The study of the kinetic parameters and enzyme stability showed a significant enhancement in the performance of the immobilized enzyme with respect to the free enzyme. The storage stability and reusability of the immobilized biocatalyst were found to be about 50 and 40% of the initial activity after 12 days and 6 cycles, respectively.
机译:使用中央复合设计(CCD)研究了α-淀粉酶的不同操作条件对磁性纳米颗粒(MNP)的影响,例如初始酶浓度,戊二醛(Ga)浓度,pH和离子强度。此外,使用Derringer的期望函数同时研究了两个反应,生物催化剂活性和固定化酶的量。将固定化酶的最佳量和活性测定为24.83%和556.41mg(MNP)( - 1),初始酶浓度为999.86ppm,溶液pH为4.6,GA浓度为0.59%,离子强度为99.99mm和4小时的过程时间。对动力学参数和酶稳定性的研究表明,固定化酶相对于游离酶的性能显着增强。发现固定化生物催化剂的储存稳定性和可重用性分别为12天和6个循环后的初始活性的约50和40%。

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  • 来源
    《RSC Advances》 |2016年第24期|共11页
  • 作者

    Eslamipour F.; Hejazi P.;

  • 作者单位

    Iran Univ Sci &

    Technol Sch Chem Engn Biotechnol Res Lab POB 16846-13114 Tehran Iran;

    Iran Univ Sci &

    Technol Sch Chem Engn Biotechnol Res Lab POB 16846-13114 Tehran Iran;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

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