Electrochemical Assay for a Total Cellulase Activity with Improved Sensitivity.

Anal Chem

Interdisciplinary Nanoscience Center, Faculty of Science and Technology, Aarhus University, Gustav Wieds Vej 14, 8000 Aarhus C, Denmark.

Published: April 2017

AI Article Synopsis

  • Electrochemical methods provide rapid and cost-effective analysis of enzymatic activities, specifically for cellulase, an enzyme used in food, textiles, and bioethanol production.
  • The developed electrochemical assay uses ferricyanide on nitrocellulose films, where cellular digestion increases electrochemical signals, revealing enzyme activity.
  • This technique shows a sensitivity of 10 U per assay and significantly outperforms traditional optical assays, making it a promising option for both research and industrial applications.

Article Abstract

Electrochemical methods allow fast and inexpensive analysis of enzymatic activities. Here, we report a simple and yet efficient electrochemical assay for the total activity of cellulase, a hydrolytic enzyme widely used in food and textiles industries, and for production of bioethanol. The assay exploits the difference in electrochemical signals from a soluble redox indicator, ferricyanide, on nitrocellulose films treated by cellulases. Ferricyanide electrochemistry is totally inhibited on graphite electrodes modified with an insulating nitrocellulose film and is evoked after the cellulase treatment. Ferricyanide voltammetric responses correlate with the increased permeability of the films and electrochemically active surface area of electrodes becoming accessible to the ferricyanide reaction after nitrocellulose digestion by cellulase. Trichoderma and Aspergillus niger cellulases activities were determined in a 5 min assay with a sensitivity of 10 U per assay, being 10-10-fold more sensitive than the standard commercially available optical assays. That makes the developed electrochemical approach the most prospective cost-effective alternative both for research and automated industrial applications.

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Source
http://dx.doi.org/10.1021/acs.analchem.6b04391DOI Listing

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