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Development of enzyme immobilized monolith micro-reactors integrated with microfluidic electrochemical cell for the evaluation of enzyme kinetics

机译:与微流电化学电池集成的固定化酶的整体式微反应器的开发,用于评估酶动力学

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This paper describes a simple and efficient method for producing an on-chip enzyme immobilized monolith micro-reactor that integrates a microfluidic electrochemical cell for rapid characterization of enzymatic kinetics. The monolith was generated using a sol-gel method, followed by PEI functionalization and enzyme immobilization via electrostatic attraction between electronegative enzymes and electropositive PEI polymers. Using the proposed immobilization strategy, a glucose oxidase (GOD) immobilized monolith micro-reactor has been produced with the controllable porosity that gives better enzyme kinetics compared to previously reported devices. This can be attributed to a favourable enzyme-substrate affinity in which more than 98% of the immobilized enzyme remains in an active conformation. The kinetic studies conducted have identified that a similar value of the k_(cat) is obtained for immobilized GOD (13.4 s~(-1)) and GOD free in solution (14 s~(-1)) whilst the immobilized Michaelis constant K_(m(app)) (7.2 mM) is ~4 times lower than GOD in solution (25 mM). In addition, the immobilized GOD exhibits increased stability, retaining at least 95% of the initial activity when stored of 30 days at 4℃, compared to only 60% for GOD in solution. Furthermore, the same enzyme immobilization strategy has been used for choline oxidase immobilization and similar kinetics to choline oxidase in solution were observed, once again indicating better maintenance of the enzyme conformation provided by the proposed method.
机译:本文介绍了一种简单有效的方法,用于生产片上固定化酶的整体式微反应器,该反应器集成了微流电化学电池,可快速表征酶动力学。使用溶胶-凝胶法生成整料,然后通过负电性酶和正电性PEI聚合物之间的静电吸引作用将PEI官能化并固定化酶。使用提出的固定化策略,已经生产了葡萄糖可氧化酶(GOD)固定的整体式微反应器,其孔隙率可控,与先前报道的设备相比,可提供更好的酶动力学。这可以归因于良好的酶-底物亲和力,其中超过98%的固定化酶保留在活性构象中。进行的动力学研究已经确定,固定化的GOD(13.4 s〜(-1))和溶液中不含GOD(14 s〜(-1))的k_(cat)值相似,而固定化的Michaelis常数K_ (m(app))(7.2 mM)比溶液中的GOD(25 mM)低约4倍。此外,固定的GOD表现出更高的稳定性,在4℃下储存30天时,其初始活性至少保持95%,而溶液中的GOD仅为60%。此外,相同的酶固定策略已用于胆碱氧化酶的固定,并观察到与溶液中胆碱氧化酶相似的动力学,再次表明所提出的方法提供的酶构象得到更好的维持。

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