Effects of Zinc Chelators on Aflatoxin Production in Aspergillus parasiticus
Zinc concentrations strongly influence aflatoxin accumulation in laboratory media and in food and feed crops. The presence of zinc stimulates aflatoxin production, and the absence of zinc impedes toxin production. Initial studies that suggested a link between zinc and aflatoxin biosynthesis were pre...
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doaj-d25981b34a4e4182bcc7a4ec2c97980c2020-11-25T01:04:29ZengMDPI AGToxins2072-66512016-06-018617110.3390/toxins8060171toxins8060171Effects of Zinc Chelators on Aflatoxin Production in Aspergillus parasiticusJosephine Wee0Devin M. Day1John E. Linz2Department of Food Science and Human Nutrition, Michigan State University, East Lansing, MI 48824, USADepartment of Food Science and Human Nutrition, Michigan State University, East Lansing, MI 48824, USADepartment of Food Science and Human Nutrition, Michigan State University, East Lansing, MI 48824, USAZinc concentrations strongly influence aflatoxin accumulation in laboratory media and in food and feed crops. The presence of zinc stimulates aflatoxin production, and the absence of zinc impedes toxin production. Initial studies that suggested a link between zinc and aflatoxin biosynthesis were presented in the 1970s. In the present study, we utilized two zinc chelators, N,N,N′,N′-tetrakis (2-pyridylmethyl) ethane-1,2-diamine (TPEN) and 2,3-dimercapto-1-propanesulfonic acid (DMPS) to explore the effect of zinc limitation on aflatoxin synthesis in Aspergillus parasiticus. TPEN but not DMPS decreased aflatoxin biosynthesis up to six-fold depending on whether A. parasiticus was grown on rich or minimal medium. Although we observed significant inhibition of aflatoxin production by TPEN, no detectable changes were observed in expression levels of the aflatoxin pathway gene ver-1 and the zinc binuclear cluster transcription factor, AflR. Treatment of growing A. parasiticus solid culture with a fluorescent zinc probe demonstrated an increase in intracellular zinc levels assessed by increases in fluorescent intensity of cultures treated with TPEN compared to controls. These data suggest that TPEN binds to cytoplasmic zinc therefore limiting fungal access to zinc. To investigate the efficacy of TPEN on food and feed crops, we found that TPEN effectively decreases aflatoxin accumulation on peanut medium but not in a sunflower seeds-derived medium. From an application perspective, these data provide the basis for biological differences that exist in the efficacy of different zinc chelators in various food and feed crops frequently contaminated by aflatoxin.http://www.mdpi.com/2072-6651/8/6/171Aspergillus parasiticusaflatoxin biosynthesiszinczinc chelators |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Josephine Wee Devin M. Day John E. Linz |
spellingShingle |
Josephine Wee Devin M. Day John E. Linz Effects of Zinc Chelators on Aflatoxin Production in Aspergillus parasiticus Toxins Aspergillus parasiticus aflatoxin biosynthesis zinc zinc chelators |
author_facet |
Josephine Wee Devin M. Day John E. Linz |
author_sort |
Josephine Wee |
title |
Effects of Zinc Chelators on Aflatoxin Production in Aspergillus parasiticus |
title_short |
Effects of Zinc Chelators on Aflatoxin Production in Aspergillus parasiticus |
title_full |
Effects of Zinc Chelators on Aflatoxin Production in Aspergillus parasiticus |
title_fullStr |
Effects of Zinc Chelators on Aflatoxin Production in Aspergillus parasiticus |
title_full_unstemmed |
Effects of Zinc Chelators on Aflatoxin Production in Aspergillus parasiticus |
title_sort |
effects of zinc chelators on aflatoxin production in aspergillus parasiticus |
publisher |
MDPI AG |
series |
Toxins |
issn |
2072-6651 |
publishDate |
2016-06-01 |
description |
Zinc concentrations strongly influence aflatoxin accumulation in laboratory media and in food and feed crops. The presence of zinc stimulates aflatoxin production, and the absence of zinc impedes toxin production. Initial studies that suggested a link between zinc and aflatoxin biosynthesis were presented in the 1970s. In the present study, we utilized two zinc chelators, N,N,N′,N′-tetrakis (2-pyridylmethyl) ethane-1,2-diamine (TPEN) and 2,3-dimercapto-1-propanesulfonic acid (DMPS) to explore the effect of zinc limitation on aflatoxin synthesis in Aspergillus parasiticus. TPEN but not DMPS decreased aflatoxin biosynthesis up to six-fold depending on whether A. parasiticus was grown on rich or minimal medium. Although we observed significant inhibition of aflatoxin production by TPEN, no detectable changes were observed in expression levels of the aflatoxin pathway gene ver-1 and the zinc binuclear cluster transcription factor, AflR. Treatment of growing A. parasiticus solid culture with a fluorescent zinc probe demonstrated an increase in intracellular zinc levels assessed by increases in fluorescent intensity of cultures treated with TPEN compared to controls. These data suggest that TPEN binds to cytoplasmic zinc therefore limiting fungal access to zinc. To investigate the efficacy of TPEN on food and feed crops, we found that TPEN effectively decreases aflatoxin accumulation on peanut medium but not in a sunflower seeds-derived medium. From an application perspective, these data provide the basis for biological differences that exist in the efficacy of different zinc chelators in various food and feed crops frequently contaminated by aflatoxin. |
topic |
Aspergillus parasiticus aflatoxin biosynthesis zinc zinc chelators |
url |
http://www.mdpi.com/2072-6651/8/6/171 |
work_keys_str_mv |
AT josephinewee effectsofzincchelatorsonaflatoxinproductioninaspergillusparasiticus AT devinmday effectsofzincchelatorsonaflatoxinproductioninaspergillusparasiticus AT johnelinz effectsofzincchelatorsonaflatoxinproductioninaspergillusparasiticus |
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