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The High-Efficiency Degradation of Multiple Mycotoxins by Lac-W Laccase in the Presence of Mediators. | LitMetric

AI Article Synopsis

  • Mycotoxin cocontamination poses significant health and economic risks globally, with six mycotoxins being particularly toxic.
  • Lac-W, an enzyme, can degrade these mycotoxins but needs enhancement for better efficiency.
  • The study finds that adding redox mediators drastically improves Lac-W's ability to degrade aflatoxin B and zearalenone quickly and safely, making it a promising solution for reducing mycotoxin contamination in food and feed.

Article Abstract

Mycotoxin cocontamination is a severe threat to health and economic security worldwide. The mycotoxins aflatoxin B (AFB), zearalenone (ZEN), deoxynivalenol, T-2 toxin, fumonisin B, and ochratoxin A are of particular concern due to their substantial toxicity. Lac-W is a laccase with the unique property of degrading these six mycotoxins in the absence of redox mediators. Nevertheless, their degradation rates are low. This work aims to improve the ability of Lac-W to degrade these six mycotoxins and to elucidate its detoxification mechanism. Including redox mediators increased the Lac-W degradation efficiency drastically, and completely degraded AFB and ZEN within one hour. Additionally, Lac-W-AS has good temperature, pH, and ions adaptability in ZEN degradation. Lac-W-AS reduced the ZEN toxicity because ZEN degradation products significantly restored the bioluminescence intensity of . A Lac-W-AS-mediated oxidation product of ZEN was structurally characterized as 15-OH-ZEN by UHPLC-MS/MS. Linear sweep voltammetry showed that AS affected the potential of Lac-W and accelerated the oxidation of ZEN. Finally, the combination of mediators (acetosyringone and 2,2'-azino-bis (3-ethylbenzothiazoline-6-sulfonate)) improved the degradation rate of mycotoxins. This work highlights that the combination of Lac-W with mediators serves as a good candidate for degrading multi-mycotoxin contaminants in food and feedstuff.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11598361PMC
http://dx.doi.org/10.3390/toxins16110477DOI Listing

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