The Metabolic Fate of Deoxynivalenol and Its Acetylated Derivatives in a Wheat Suspension Culture: Identification and Detection of DON-15-O-Glucoside, 15-Acetyl-DON-3-O-Glucoside and 15-Acetyl-DON-3-Sulfate
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Deoxynivalenol (DON) is a protein synthesis inhibitor produced by the Fusarium species, which frequently contaminates grains used for human or animal consumption. We treated a wheat suspension culture with DON or one of its acetylated derivatives, 3-acetyl-DON (3-ADON), 15-acetyl-DON (15-ADON) and 3,15-diacetyl-DON (3,15-diADON), and monitored the metabolization over a course of 96 h. Supernatant and cell extract samples were analyzed using a tailored LC-MS/MS method for the quantification of DON metabolites. We report the formation of tentatively identified DON-15-O-β-D-glucoside (D15G) and of 15-acetyl-DON-3-sulfate (15-ADON3S) as novel deoxynivalenol metabolites in wheat. Furthermore, we found that the recently identified 15-acetyl-DON-3-O-β-D-glucoside (15-ADON3G) is the major metabolite produced after 15-ADON challenge. 3-ADON treatment led to a higher intracellular content of toxic metabolites after six hours compared to all other treatments. 3-ADON was exclusively metabolized into DON before phase II reactions occurred. In contrast, we found that 15-ADON was directly converted into 15-ADON3G and 15-ADON3S in addition to metabolization into deoxynivalenol-3-O-β-D-glucoside (D3G). This study highlights significant differences in the metabolization of DON and its acetylated derivatives.
Yulfo-Soto G, McCormick S, Chen H, Bai G, Trick H, Hao G Front Plant Sci. 2024; 15:1389605.
PMID: 38650698 PMC: 11033581. DOI: 10.3389/fpls.2024.1389605.
Anastasiadis V, Raptis I, Economou A, Kakabakos S, Petrou P Biosensors (Basel). 2020; 10(11).
PMID: 33113758 PMC: 7692517. DOI: 10.3390/bios10110154.
Flasch M, Bueschl C, Woelflingseder L, Schwartz-Zimmermann H, Adam G, Schuhmacher R ACS Chem Biol. 2020; 15(4):970-981.
PMID: 32167285 PMC: 7171601. DOI: 10.1021/acschembio.9b01016.
Bryla M, Waskiewicz A, Ksieniewicz-Wozniak E, Szymczyk K, Jedrzejczak R Molecules. 2018; 23(4).
PMID: 29677133 PMC: 6017960. DOI: 10.3390/molecules23040963.
Michlmayr H, Varga E, Malachova A, Fruhmann P, Piatkowska M, Hametner C Toxins (Basel). 2018; 10(3).
PMID: 29509722 PMC: 5869399. DOI: 10.3390/toxins10030111.