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首页> 外文期刊>Nanotechnology >The on-line synthesis of enzyme functionalized silica nanoparticles in a microfluidic reactor using polyethylenimine polymer and R5 peptide
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The on-line synthesis of enzyme functionalized silica nanoparticles in a microfluidic reactor using polyethylenimine polymer and R5 peptide

机译:使用聚乙烯亚胺聚合物和R5肽在微流控反应器中在线合成酶功能化二氧化硅纳米粒子

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摘要

A simple microfluidic reactor system is described for the effective synthesis of enzyme functionalized nanoparticles which offers many advantages over batch reactions, including excellent enzyme efficiencies. Better control of the process parameters in the microfluidic reactor system over batch based methodology enables the production of silica nanoparticles with the optimum size for efficient enzyme immobilization with long-term stability. The synthetic approach is demonstrated with glucose oxidase (GOD) and two different nucleation catalysts of similar molecular mass: the natural R5 peptide, and polyethylenimine (PEI) polymer. Near-quantitative immobilization of GOD in the nanoparticles is obtained using PEI; the immobilization is attributed to electrostatic interaction between PEI and GOD. This interaction, however, limits the mobility of the immobilized enzyme, producing orientation hindrance of the enzyme's active sites as compared to free GOD in solution. In contrast, when the GOD is immobilized inside the silica nanoparticles using R5, lower enzyme immobilization efficiencies are obtained compared to using PEI polymers; however, similar Michaelis -Menten kinetic parameters (i.e. Michaelis constant and turnover number) to those of free GOD are observed. Reactions were monitored in situ using simple, rapid, separation-free amperometric detection.
机译:描述了一种简单的微流体反应器系统,用于有效合成酶功能化的纳米粒子,与批反应相比,该系统具有许多优势,包括出色的酶效率。通过基于批处理的方法更好地控制微流体反应器系统中的工艺参数,可以生产具有最佳尺寸的二氧化硅纳米粒子,以实现具有长期稳定性的有效酶固定。用葡萄糖氧化酶(GOD)和两种不同分子量相似的成核催化剂证明了合成方法:天然R5肽和聚乙烯亚胺(PEI)聚合物。使用PEI获得了近乎定量的GOD在纳米颗粒中的固定化。固定化归因于PEI和GOD之间的静电相互作用。然而,与溶液中的游离GOD相比,这种相互作用限制了固定化酶的移动性,产生了酶活性位点的取向障碍。相反,当使用R5将GOD固定在二氧化硅纳米颗粒内部时,与使用PEI聚合物相比,获得的酶固定效率较低;然而,观察到与游离GOD相似的Michaelis-Menten动力学参数(即Michaelis常数和周转数)。使用简单,快速,无分离的安培检测法对反应进行原位监测。

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