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1.
J Agric Food Chem ; 69(5): 1684-1692, 2021 Feb 10.
Artículo en Inglés | MEDLINE | ID: mdl-33522237

RESUMEN

In recent years, deoxynivalenol (DON) has frequently been detected in wheat grains and their products. The enantioselective impact of flutriafol on the growth and DON biosynthesis of Fusarium graminearum was investigated in relation to water activity (αw, 0.97 and 0.99) and temperature (20, 25, and 30 °C) on the wheat-based medium. R-(-)-flutriafol exhibited higher bioactivity than S-(+)-flutriafol and Rac-flutriafol under the above conditions. Flutriafol enantiomers reduced or stimulated DON biosynthesis depending on αw. DON levels were negligible after 14 or 7 days of incubation times under 0.97 and 0.99 aw, respectively. Quantitative real-time polymerase chain reaction (qRT-PCR) analyses showed that the expression levels of trichothecene biosynthetic (TRI) genes of F. graminearum under 0.97 aw were significantly higher than those under 0.99 aw. In addition, R-(-)-flutriafol can induce more TRI gene expression than S-(+)-flutriafol. Taken together, this study indicated that aw and temperature play important roles in regulating DON biosynthesis in F. graminearum with flutriafol enantiomers.


Asunto(s)
Fungicidas Industriales/química , Fungicidas Industriales/farmacología , Fusarium/efectos de los fármacos , Fusarium/crecimiento & desarrollo , Triazoles/química , Triazoles/farmacología , Tricotecenos/metabolismo , Proteínas Fúngicas/genética , Proteínas Fúngicas/metabolismo , Fusarium/genética , Fusarium/metabolismo , Regulación Fúngica de la Expresión Génica/efectos de los fármacos , Enfermedades de las Plantas/microbiología , Estereoisomerismo , Triticum/microbiología
2.
J Hazard Mater ; 284: 65-72, 2015 Mar 02.
Artículo en Inglés | MEDLINE | ID: mdl-25463219

RESUMEN

The enantioselective bioactivity, acute toxicity and stereoselective degradation of the chiral triazole fungicide flutriafol in vegetables were investigated for the first time using the (R)-, (S)- and rac-flutriafol. The order of the bioactivity against five target pathogens (Rhizoctonia solani, Alternaria solani, Pyricularia grisea, Gibberella zeae, Botrytis cinerea) was found to be (R)-flutriafol>rac-flutriafol>(S)-flutriafol. The fungicidal activity of (R)-flutriafol was 1.49-6.23 times higher than that of (S)-flutriafol. The (R)-flutriafol also showed 2.17-3.52 times higher acute toxicity to Eisenia fetida and Scenedesmus obliquus than (S)-flutriafol. The stereoselective degradation of flutriafol in tomato showed that the active (R)-flutriafol degraded faster, resulting in an enrichment of inactive (S)-form, and the half-lives were 9.23 d and 10.18 d, respectively. Inversely, the (S)-flutriafol, with a half-life of 4.76 d, was preferentially degraded in cucumber. In conclusion, the systemic assessments of the triazole fungicide flutriafol stereoisomers on the enantioselective bioactivity, acute toxicity and environmental behavior may have implications for better environmental and ecological risk assessment.


Asunto(s)
Fungicidas Industriales/química , Fungicidas Industriales/toxicidad , Triazoles/química , Alternaria , Animales , Botrytis , Calibración , Cromatografía Líquida de Alta Presión , Cucumis sativus , Ecología , Gibberella , Solanum lycopersicum , Oligoquetos , Rhizoctonia , Medición de Riesgo , Estereoisomerismo , Triazoles/toxicidad , Verduras
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