Navigating Side Reactions for Robust Colorimetric Detection of Galactose Oxidase Activity

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Navigating Side Reactions for Robust Colorimetric Detection of Galactose Oxidase Activity
Title:
Navigating Side Reactions for Robust Colorimetric Detection of Galactose Oxidase Activity
Journal Title:
Analytical Chemistry
Publication Date:
01 March 2025
Citation:
Koo, Y. S., Chen, A. X., Tay, C. Y. J., Wang, V. Y. E., See, J. Y., Lim, Y. H., & Tay, D. W. P. (2025). Navigating Side Reactions for Robust Colorimetric Detection of Galactose Oxidase Activity. Analytical Chemistry. https://doi.org/10.1021/acs.analchem.4c07034
Abstract:
Colorimetric assays are a rapid, scalable technique well suited for enzyme activity screening. However, side reactions or chromogenic reagent instability can result in false positives or false negatives that compromise the accuracy of such assays. Here, we identify three classes of compounds incompatible with the 2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) colorimetric assay for galactose oxidase activity. Dark green ABTS•+ cationic radicals indicating enzyme activity can get quenched to yield colorless solutions or couple with substrates to form differently colored adducts, thus preventing accurate colorimetric measurements. These side reactions limit the utility of the ABTS assay and introduce uncertainty on the substrate scope it is applicable to. We have investigated the underlying mechanisms behind these side reactions to conclude that free radical scavengers, phenols with electron-donating substituents, and beta-gamma-unsaturated aryl ketones are incompatible with the ABTS colorimetric assay. In search of a viable alternative, we have developed an assay using 2,4-dinitrophenylhydrazine under neutral conditions with isopropyl alcohol as a solubilizing agent. The use of neutral conditions was found to be critical to avoid hydrolysis of hydrazone adducts, ensuring reproducible measurements. Our assay is compatible with free radical scavengers (R2 = 0.98), phenols with electron-donating substituents (R2 = 0.97), and beta-gamma-unsaturated aryl ketones (R2 = 0.88). This modified assay enables galactose oxidase activity screening across a broader substrate scope, thus facilitating enzyme use for more practical applications.
License type:
Publisher Copyright
Funding Info:
This research / project is supported by the Agency for Science, Technology and Research (A*STAR), Singapore - Advanced Manufacturing and Engineering (AME) Industry Alignment Fund Pre-positioning (IAF-PP) PIPS
Grant Reference no. : A19B3a0009

This research / project is supported by the Agency for Science, Technology and Research (A*STAR), Singapore - Manufacturing Trade and Connectivity (MTC) Individual Research Grant (IRG)
Grant Reference no. : M22K2c0086

This research / project is supported by the Agency for Science, Technology and Research (A*STAR), Singapore - Advanced Manufacturing and Engineering (AME) SERC Strategic Funds
Grant Reference no. : A1718g0092
Description:
This document is the Accepted Manuscript version of a Published Work that appeared in final form in Analytical Chemistry, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see 10.1021/acs.analchem.4c07034.
ISSN:
0003-2700
1520-6882
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