Cleavage of Zearalenone by Trichosporon mycotoxinivorans to a Novel Nonestrogenic Metabolite

• Published in: Applied and Environmental Microbiology 2010-04, Vol.76 (7), p.2353-2359
• Main Authors: Vekiru, Elisavet, Hametner, Christian, Mitterbauer, Rudolf, Rechthaler, Justyna, Adam, Gerhard, Schatzmayr, Gerd, Krska, Rudolf, Schuhmacher, Rainer
• Format: Article
• Language: English
• Subjects: Biofuels; Biological and medical sciences; Biotransformation; Chromatography, Liquid; Corn; Estrogens; Fundamental and applied biological sciences. Psychology; Fusarium; Magnetic Resonance Spectroscopy; Microbiology; Molecular Weight; Mycology; NMR; Nuclear magnetic resonance; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Spectrum analysis; Steroids - chemistry; Steroids - metabolism; Tandem Mass Spectrometry; Toxins; Trichosporon - metabolism; Yeast; Zearalenone - antagonists & inhibitors; Zearalenone - metabolism
• ISSN: 0099-2240; 1098-5336; 1098-6596
• DOI: 10.1128/AEM.01438-09

Zearalenone (ZON) is a potent estrogenic mycotoxin produced by several Fusarium species most frequently on maize and therefore can be found in food and animal feed. Since animal production performance is negatively affected by the presence of ZON, its detoxification in contaminated plant material or by-products of bioethanol production would be advantageous. Microbial biotransformation into nontoxic metabolites is one promising approach. In this study the main transformation product of ZON formed by the yeast Trichosporon mycotoxinivorans was identified and characterized by liquid chromatography-tandem mass spectrometry (LC-MS/MS) and LC-diode array detector (DAD) analysis. The metabolite, named ZOM-1, was purified, and its molecular formula, C₁₈H₂₄O₇, was established by time of flight MS (TOF MS) from the ions observed at m/z 351.1445 [M-H]⁻ and at m/z 375.1416 [M+Na]⁺. Employing nuclear magnetic resonance (NMR) spectroscopy, the novel ZON metabolite was finally identified as (5S)-5-({2,4-dihydroxy-6-[(1E)-5-hydroxypent-1-en-1-yl]benzoyl}oxy)hexanoic acid. The structure of ZOM-1 is characterized by an opening of the macrocyclic ring of ZON at the ketone group at C6'. ZOM-1 did not show estrogenic activity in a sensitive yeast bioassay, even at a concentration 1,000-fold higher than that of ZON and did not interact with the human estrogen receptor in an in vitro competitive binding assay.