Literature DB >> 11665729

Stability of the fusarium mycotoxins nivalenol, deoxynivalenol and zearalenone in ground maize under typical cooking environments.

D R Lauren1, W A Smith.   

Abstract

The effects of moisture, pH and heat on the stability of nivalenol (NIV), deoxtnivalenol (DON) and zearalenone (ZEN) present as natural contaminants of ground maize were measured for different periods. Standard solution tests were also performed to measure pH, salt and temperature effects on NIV and DON. The solution tests showed NIV and DON to be relatively stable in buffer solutions over the pH range 1-10. Quite harsh conditions (pH 12, high salt concentration, 80 degrees C, prolonged exposure) were needed to give substantial breakdown. In the ground maize substrate, these toxins were further stabilized relative to the solution tests. NIV and DON were both reduced (range 60-100%) by treatment with aqueous bicarbonate solution at 10, 20 or 50% of the ground maize dry weight, and subsequent heating at 80 or 110 degrees C for 2 and 12 days. There was no measurable reduction at lower test temperatures (20, 40 degrees C). NIV (but not DON) also showed some reduction following addition of water and heating at 80 or 110 degrees C for 12 days. ZEN content was not reduced even by 12 days of heating at 110 degrees C after treatment with a sodium bicarbonate solution.

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Year:  2001        PMID: 11665729     DOI: 10.1080/02652030110052283

Source DB:  PubMed          Journal:  Food Addit Contam        ISSN: 0265-203X


  13 in total

1.  Characterization of deoxynivalenol-induced anorexia using mouse bioassay.

Authors:  Brenna M Flannery; Wenda Wu; James J Pestka
Journal:  Food Chem Toxicol       Date:  2011-05-07       Impact factor: 6.023

2.  Reduction of deoxynivalenol in barley by treatment with aqueous sodium carbonate and heat.

Authors:  David Abramson; James D House; C Martin Nyachoti
Journal:  Mycopathologia       Date:  2005-11       Impact factor: 2.574

3.  Nocardioides sp. strain WSN05-2, isolated from a wheat field, degrades deoxynivalenol, producing the novel intermediate 3-epi-deoxynivalenol.

Authors:  Yoko Ikunaga; Ikuo Sato; Stephanie Grond; Nobutaka Numaziri; Shigenobu Yoshida; Hiroko Yamaya; Syuntaro Hiradate; Morifumi Hasegawa; Hiroaki Toshima; Motoo Koitabashi; Michihiro Ito; Petr Karlovsky; Seiya Tsushima
Journal:  Appl Microbiol Biotechnol       Date:  2010-09-21       Impact factor: 4.813

4.  [Isolation and structural elucidation of thermal degradation products of theFusarium mycotoxin nivalenol].

Authors:  M Bretz; S Göckler; H U Humpf
Journal:  Mycotoxin Res       Date:  2005-03       Impact factor: 3.833

5.  Microbial Detoxification of Deoxynivalenol (DON), Assessed via a Lemna minor L. Bioassay, through Biotransformation to 3-epi-DON and 3-epi-DOM-1.

Authors:  Ilse Vanhoutte; Laura De Mets; Marthe De Boevre; Valdet Uka; José Diana Di Mavungu; Sarah De Saeger; Leen De Gelder; Kris Audenaert
Journal:  Toxins (Basel)       Date:  2017-02-13       Impact factor: 4.546

6.  The Antagonistic Effect of Mycotoxins Deoxynivalenol and Zearalenone on Metabolic Profiling in Serum and Liver of Mice.

Authors:  Jian Ji; Pei Zhu; Fangchao Cui; Fuwei Pi; Yinzhi Zhang; Yun Li; Jiasheng Wang; Xiulan Sun
Journal:  Toxins (Basel)       Date:  2017-01-10       Impact factor: 4.546

7.  Stability of Mycotoxins in Individual Stock and Multi-Analyte Standard Solutions.

Authors:  Mariya Kiseleva; Zakhar Chalyy; Irina Sedova; Ilya Aksenov
Journal:  Toxins (Basel)       Date:  2020-01-30       Impact factor: 4.546

8.  Inhibition of mycotoxin-producing Aspergillus nomius vsc 23 by lactic acid bacteria and Saccharomyces cerevisiae.

Authors:  R Muñoz; M E Arena; J Silva; S N González
Journal:  Braz J Microbiol       Date:  2010-12-01       Impact factor: 2.476

9.  Isolation and identification of a strain of Aspergillus tubingensis with deoxynivalenol biotransformation capability.

Authors:  Chenghua He; Yanhong Fan; Guofang Liu; Haibin Zhang
Journal:  Int J Mol Sci       Date:  2008-11-27       Impact factor: 6.208

10.  Fumonisins, trichothecenes and zearalenone in cereals.

Authors:  Selma Yazar; Gülden Z Omurtag
Journal:  Int J Mol Sci       Date:  2008-10-31       Impact factor: 6.208

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