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用于在生物催化流动反应器中可控生产过氧化氢的葡萄糖氧化酶的电化学固定化

Electrochemical Immobilisation of Glucose Oxidase for the Controlled Production of HO in a Biocatalytic Flow Reactor.

作者信息

Arshi Simin, Xiao Xinxin, Belochapkine Serguei, Magner Edmond

机构信息

Department of Chemical Sciences Bernal Institute University of Limerick V94 T9PX Limerick Ireland.

Department of Chemistry Technical University of Denmark Kongens Lyngby 2800 Denmark.

出版信息

ChemElectroChem. 2022 Sep 13;9(17):e202200319. doi: 10.1002/celc.202200319. Epub 2022 Sep 8.

Abstract

Electrochemical methods can be used to selectively modify the surfaces of electrodes, enabling the immobilisation of enzymes on defined areas on the surfaces of electrodes. Such selective immobilisation methods can be used to pattern catalysts on surfaces in a controlled manner. Using this approach, the selective patterning of the enzyme glucose oxidase on the electrodes was used to develop a flow reactor for the controlled delivery of the oxidant HO. GOx was immobilised on a glassy carbon electrode using polypyrrole, silica films, and diazonium linkers. The rate of production of HO and the stability of the response was dependent on the immobilisation method. GOx encapsulated in polypyrrole was selected as the optimal method of immobilisation, with a rate of production of 91±11 μM h for 4 hours of continuous operation. The enzyme was subsequently immobilised on carbon rod electrodes (surface area of 5.76 cm) using a polypyrrole/Nafion® film and incorporated into a flow reactor. The rate of production of HO was 602±57 μM h, with 100 % retention of activity after 7 h of continuous operation, demonstrating that such a system can be used to prepare HO at continuous and stable rate for use in downstream oxidation reactions.

摘要

电化学方法可用于选择性地修饰电极表面,从而使酶能够固定在电极表面的特定区域。这种选择性固定方法可用于以可控方式在表面上对催化剂进行图案化。利用这种方法,通过在电极上对葡萄糖氧化酶进行选择性图案化,开发了一种用于可控输送氧化剂HO的流动反应器。使用聚吡咯、二氧化硅膜和重氮连接剂将葡萄糖氧化酶固定在玻碳电极上。HO的产生速率和响应稳定性取决于固定方法。封装在聚吡咯中的葡萄糖氧化酶被选为最佳固定方法,连续运行4小时的产生速率为91±11 μM·h。随后,使用聚吡咯/全氟磺酸膜将该酶固定在碳棒电极(表面积为5.76 cm)上,并将其纳入流动反应器中。HO的产生速率为602±57 μM·h,连续运行7小时后活性保留100%,表明该系统可用于以连续稳定的速率制备HO,用于下游氧化反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b0/9545823/2bf1679037b9/CELC-9-0-g002.jpg

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