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Published on: April 23, 2012
Nitrogen repression of fumonisin B1 biosynthesis in Gibberella fujikuroi
1Department of Botany and Plant Pathology, Purdue University, West Lafayette, IN 47907, USA.
Abstract:
Fumonisins are a group of structurally related mycotoxins produced by Gibberella fujikuroi. The fungus produced fumonisin B1 (FB1) as early as 18 hour in a defined medium containing 1.25 mM or 2.5 mM ammonium phosphate, whereas fumonisin B1 production was repressed for 75 hour and 125 hour when mycelia were resuspended in media containing ammonium phosphate at 10 mM or 20 mM, respectively. Although total fumonisin B1 production was greater in resuspension cultures grown in higher concentrations of ammonium phosphate, the accumulation was independent of the inoculum size and carbon/nitrogen ratio. The addition of ammonium phosphate to cracked corn cultures also repressed fumonisin B1 production by 97%, and persisted for at least three weeks. Thus, biosynthesis of fumonisin B1 is regulated by a mechanism involving nitrogen metabolite repression, suggesting that control strategies that target the regulatory elements of nitrogen metabolism may be effective at reducing the risk of fumonisin contamination in food.
Insights
High nitrogen levels, specifically ammonium phosphate, significantly repress fumonisin B1 (FB1) production in fungi. This nitrogen metabolite repression suggests strategies targeting nitrogen metabolism can reduce fumonisin contamination in food.
Area of Science:
- Mycology
- Food Science
- Biochemistry
Background:
- Fumonisins are mycotoxins produced by the fungus Gibberella fujikuroi.
- Fumonisin B1 (FB1) is a major concern due to its potential toxicity.
Purpose of the Study:
- To investigate the effect of ammonium phosphate concentration on fumonisin B1 production.
- To understand the regulatory mechanisms controlling fumonisin biosynthesis.
Main Methods:
- Culturing Gibberella fujikuroi in defined media with varying ammonium phosphate concentrations.
- Resuspending mycelia in media with different nitrogen levels.
- Analyzing FB1 production in cracked corn cultures with ammonium phosphate addition.
Main Results:
- Ammonium phosphate repressed FB1 production, with repression duration increasing at higher concentrations (10 mM and 20 mM).
- Total FB1 production was higher in resuspension cultures with increased ammonium phosphate, but accumulation was independent of inoculum size and C/N ratio.
- Addition of ammonium phosphate to cracked corn cultures reduced FB1 production by 97%.
Conclusions:
- Fumonisin B1 biosynthesis is regulated by nitrogen metabolite repression.
- Targeting nitrogen metabolism pathways offers a potential strategy to control fumonisin contamination in food products.
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