Literature DB >> 24746119

Polyethyleneimine as a promoter layer for the immobilization of cellobiose dehydrogenase from Myriococcum thermophilum on graphite electrodes.

Christopher Schulz1, Roland Ludwig, Lo Gorton.   

Abstract

Cellobiose dehydrogenase (CDH) is a promising enzyme for the construction of biofuel cell anodes and biosensors capable of oxidizing aldoses as cellobiose as well as lactose and glucose and with the ability to connect to an electrode through a direct electron transfer mechanism. In the present study, we point out the beneficial effect of a premodification of spectrographic graphite electrodes with the polycation polyethyleneimine (PEI) prior to adsorption of CDH from Myriococcum thermophilum (MtCDH). The application of PEI shifts the pH optimum of the response of the MtCDH modified electrode from pH 5.5 to 8. The catalytic currents to lactose were increased up to 140 times, and the K(M)(app) values were increased up to 9 times. The previously investigated, beneficial effect of divalent cations on the activity of CDH was also present for graphite/PEI/MtCDH electrodes but was less pronounced. Polarization curves revealed a second unexpected catalytic wave for graphite/PEI/MtCDH electrodes especially pronounced at pH 8. Square wave voltammetric studies revealed the presence of an unknown redox functionality present at 192 mV vs Ag|AgCl (0.1 M KCl) at pH 8, probably originating from an oxidized adenosine derivative. Adenosine is a structural part of the flavin adenine dinucleotide (FAD) cofactor of the dehydrogenase domain of CDH. It is suggested that for some enzyme molecules FAD leaks out from the active site, adsorbs onto graphite, and is oxidized on the electrode surface into a product able to mediate the electron transfer between CDH and the electrode. PEI is suggested and discussed to act in several manners by (a) increasing the surface loading of the enzyme, (b) possibly increasing the electron transfer rate between CDH and the electrode, and (c) facilitating the creation or immobilization of redox active adenosine derivatives able to additionally mediate the electron transfer between CDH and the electrode.

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Year:  2014        PMID: 24746119     DOI: 10.1021/ac403957t

Source DB:  PubMed          Journal:  Anal Chem        ISSN: 0003-2700            Impact factor:   6.986


  5 in total

1.  Studying direct electron transfer by site-directed immobilization of cellobiose dehydrogenase.

Authors:  Marta Meneghello; Firas A Al-Lolage; Su Ma; Roland Ludwig; Philip N Bartlett
Journal:  ChemElectroChem       Date:  2019-01-30       Impact factor: 4.590

Review 2.  Cellobiose dehydrogenase in biofuel cells.

Authors:  Stefan Scheiblbrandner; Florian Csarman; Roland Ludwig
Journal:  Curr Opin Biotechnol       Date:  2021-09-03       Impact factor: 10.279

3.  Bioinspired Immobilization of Glycerol Dehydrogenase by Metal Ion-Chelated Polyethyleneimines as Artificial Polypeptides.

Authors:  Yonghui Zhang; Hong Ren; Yali Wang; Kainan Chen; Baishan Fang; Shizhen Wang
Journal:  Sci Rep       Date:  2016-04-07       Impact factor: 4.379

4.  A Third Generation Glucose Biosensor Based on Cellobiose Dehydrogenase Immobilized on a Glassy Carbon Electrode Decorated with Electrodeposited Gold Nanoparticles: Characterization and Application in Human Saliva.

Authors:  Paolo Bollella; Lo Gorton; Roland Ludwig; Riccarda Antiochia
Journal:  Sensors (Basel)       Date:  2017-08-18       Impact factor: 3.576

5.  The influence of pH and divalent/monovalent cations on the internal electron transfer (IET), enzymatic activity, and structure of fructose dehydrogenase.

Authors:  Paolo Bollella; Yuya Hibino; Kenji Kano; Lo Gorton; Riccarda Antiochia
Journal:  Anal Bioanal Chem       Date:  2018-03-22       Impact factor: 4.142

  5 in total

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