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Low Toxicity of Deoxynivalenol-3-Glucoside in Microbial Cells

Host plants excrete a glucosylation enzyme onto the plant surface that changes mycotoxins derived from fungal secondary metabolites to glucosylated products. Deoxynivalenol-3-glucoside (DON3G) is synthesized by grain uridine diphosphate-glucosyltransferase, and is found worldwide, although informati...

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Autores principales: Suzuki, Tadahiro, Iwahashi, Yumiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4303822/
https://www.ncbi.nlm.nih.gov/pubmed/25609182
http://dx.doi.org/10.3390/toxins7010187
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author Suzuki, Tadahiro
Iwahashi, Yumiko
author_facet Suzuki, Tadahiro
Iwahashi, Yumiko
author_sort Suzuki, Tadahiro
collection PubMed
description Host plants excrete a glucosylation enzyme onto the plant surface that changes mycotoxins derived from fungal secondary metabolites to glucosylated products. Deoxynivalenol-3-glucoside (DON3G) is synthesized by grain uridine diphosphate-glucosyltransferase, and is found worldwide, although information on its toxicity is lacking. Here, we conducted growth tests and DNA microarray analysis to elucidate the characteristics of DON3G. The Saccharomyces cerevisiae PDR5 mutant strain exposed to DON3G demonstrated similar growth to the dimethyl sulfoxide control, and DNA microarray analysis revealed limited differences. Only 10 genes were extracted, and the expression profile of stress response genes was similar to that of DON, in contrast to metabolism genes like SER3, which encodes 3-phosphoglycerate dehydrogenase. Growth tests with Chlamydomonas reinhardtii also showed a similar growth rate to the control sample. These results suggest that DON3G has extremely low toxicity to these cells, and the glucosylation of mycotoxins is a useful protective mechanism not only for host plants, but also for other species.
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spelling pubmed-43038222015-02-02 Low Toxicity of Deoxynivalenol-3-Glucoside in Microbial Cells Suzuki, Tadahiro Iwahashi, Yumiko Toxins (Basel) Article Host plants excrete a glucosylation enzyme onto the plant surface that changes mycotoxins derived from fungal secondary metabolites to glucosylated products. Deoxynivalenol-3-glucoside (DON3G) is synthesized by grain uridine diphosphate-glucosyltransferase, and is found worldwide, although information on its toxicity is lacking. Here, we conducted growth tests and DNA microarray analysis to elucidate the characteristics of DON3G. The Saccharomyces cerevisiae PDR5 mutant strain exposed to DON3G demonstrated similar growth to the dimethyl sulfoxide control, and DNA microarray analysis revealed limited differences. Only 10 genes were extracted, and the expression profile of stress response genes was similar to that of DON, in contrast to metabolism genes like SER3, which encodes 3-phosphoglycerate dehydrogenase. Growth tests with Chlamydomonas reinhardtii also showed a similar growth rate to the control sample. These results suggest that DON3G has extremely low toxicity to these cells, and the glucosylation of mycotoxins is a useful protective mechanism not only for host plants, but also for other species. MDPI 2015-01-20 /pmc/articles/PMC4303822/ /pubmed/25609182 http://dx.doi.org/10.3390/toxins7010187 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Suzuki, Tadahiro
Iwahashi, Yumiko
Low Toxicity of Deoxynivalenol-3-Glucoside in Microbial Cells
title Low Toxicity of Deoxynivalenol-3-Glucoside in Microbial Cells
title_full Low Toxicity of Deoxynivalenol-3-Glucoside in Microbial Cells
title_fullStr Low Toxicity of Deoxynivalenol-3-Glucoside in Microbial Cells
title_full_unstemmed Low Toxicity of Deoxynivalenol-3-Glucoside in Microbial Cells
title_short Low Toxicity of Deoxynivalenol-3-Glucoside in Microbial Cells
title_sort low toxicity of deoxynivalenol-3-glucoside in microbial cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4303822/
https://www.ncbi.nlm.nih.gov/pubmed/25609182
http://dx.doi.org/10.3390/toxins7010187
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