Results 11 to 20 of about 10,139 (158)

Reduced toxicity of 3-epi-deoxynivalenol and de-epoxy-deoxynivalenol through deoxynivalenol bacterial biotransformation: In vivo analysis in piglets

open access: yesFood and Chemical Toxicology, 2020
International audienceIngestion of deoxynivalenol (DON), one of the most common mycotoxin contaminants of cereals, leads to adverse effects for animal and human health. Bacterial biotransformation is a strategy to mitigate the toxicity of this mycotoxin.
Gerez, Juliana, R   +8 more
core   +4 more sources

Nucleophilic Addition of Thiols to Deoxynivalenol [PDF]

open access: yesJournal of Agricultural and Food Chemistry, 2015
Conjugation of deoxynivalenol (DON) with sulfur compounds is recognized as a significant reaction pathway, and putative DON–glutathione (DON–GSH) conjugates have been reported in planta.
Alistair L. Wilkins   +19 more
core   +6 more sources

Chemical Synthesis of Deoxynivalenol-3-β-d-[13C6]-glucoside and Application in Stable Isotope Dilution Assays

open access: yesMolecules, 2016
Modified mycotoxins have been gaining importance in recent years and present a certain challenge in LC-MS/MS analysis. Due to the previous lack of a labeled isotopologue of the modified mycotoxin deoxynivalenol-3-glucoside, in our study we synthesized ...
Katharina Habler   +2 more
doaj   +2 more sources

Monitoring of the occurrence of deoxynivalenol in beers from outlet shops in 2009-2012.

open access: yesKvasný průmysl, 2013
In 2009-2012, the occurrence of mycotoxin deoxynivalenol in beer samples from Czech outlet shops was monitored . Samples included pale, dark, dispensed, lager and non-alcoholic beers .
Sylvie BĚLÁKOVÁ   +4 more
doaj   +2 more sources

Lauric acid reduces apoptosis by inhibiting FOXO3a-signaling in deoxynivalenol-treated IPEC-J2 cells

open access: yesJournal of Animal Science and Technology
Deoxynivalenol (DON) is the most common mycotoxin contaminant of food or feed worldwide and causes disease in animals. Lauric acid (LA) is a medium-chain fatty acid useful for barrier functions such as antimicrobial activity in the intestine of ...
Na Yeon Kim, Sang In Lee
doaj   +2 more sources

Analytical Strategies for the Determination of Deoxynivalenol and its Modified Forms in Beer: A Mini Review [PDF]

open access: yesKvasný průmysl, 2015
The aim of this review is to provide a brief overview of analytical methods used for the determination of deoxynivalenol and its modified forms deoxynivalenol-3-β-D-glucoside, 3-acetyl-deoxynivalenol and 15-acetyl-deoxynivalenol in beer.
Alexandra Malachová   +3 more
doaj   +2 more sources

Analysis of the regulatory mechanism of deoxynivalenol production using omics

open access: yesAMB Express, 2018
Fusarium species are plant pathogens that produce various mycotoxins. Here, the regulatory mechanism of deoxynivalenol production in Fusarium asiaticum was analyzed using proteomic, metabolomic and transcriptomic methods. F.
Yumiko Iwahashi
doaj   +2 more sources

Conversion of Deoxynivalenol-3-Glucoside to Deoxynivalenol during Chinese Steamed Bread Processing [PDF]

open access: yesToxins, 2020
We reported the conversion of deoxynivalenol-3-glucoside (D3G) to deoxynivalenol (DON) during Chinese steamed bread (CSB) processing by artificial D3G contamination.
Weixi Li   +8 more
core   +4 more sources

Phage Display Selection of an Anti-Idiotype-Antibody with Broad-Specificity to Deoxynivalenol Mycotoxins [PDF]

open access: yesToxins, 2020
The use of synthetic antibody libraries and phage displays provides an efficient and robust method for the generation of antibodies against a wide range of targets with highly specific binding properties.
Janne Leivo   +2 more
doaj   +2 more sources

Enzymatic synthesis of the modified mycotoxins 3-lactyl- and 3-propionyl-deoxynivalenol

open access: yesFrontiers in Sustainable Food Systems
The use of lactic acid bacteria as a low-cost sustainable management tool to prevent further build-up of Fusarium mycotoxins during grain storage is increasingly propagated.
Herbert Michlmayr   +7 more
doaj   +2 more sources

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