Nitrogen repression of fumonisin B1 biosynthesis in Gibberella fujikuroi

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 myce...

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Veröffentlicht in:FEMS microbiology letters 1999-08, Vol.177 (1), p.109-116
Hauptverfasser: Shim, W.B, Woloshuk, C.P
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description 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.
doi_str_mv 10.1111/j.1574-6968.1999.tb13720.x
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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.</description><identifier>ISSN: 0378-1097</identifier><identifier>EISSN: 1574-6968</identifier><identifier>DOI: 10.1111/j.1574-6968.1999.tb13720.x</identifier><identifier>PMID: 10436928</identifier><identifier>CODEN: FMLED7</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Ammonium ; Ammonium phosphates ; Biological and medical sciences ; Biosynthesis ; Carbon/nitrogen ratio ; Carboxylic Acids - metabolism ; Corn ; Culture Media ; Food contamination ; Fumonisin ; Fumonisin B1 ; Fumonisins ; Fundamental and applied biological sciences. Psychology ; Fungal plant pathogens ; Fungi ; Fusarium moniliforme ; Gibberella - drug effects ; Gibberella - growth &amp; development ; Gibberella - metabolism ; Gibberella fujikuroi ; Inoculum ; Kinetics ; Metabolites ; Microbiology ; Mycelia ; Mycology ; Mycotoxin ; Mycotoxins ; Mycotoxins - biosynthesis ; Nitrogen ; Nitrogen - metabolism ; Nitrogen metabolite repression ; Pathogenicity, host-agent relations, miscellaneous strains, epidemiology ; Phosphates - metabolism ; Phosphates - pharmacology ; Phytopathology. Animal pests. Plant and forest protection ; plant pathogenic fungi ; Regulatory sequences ; Risk reduction ; Sucrose - metabolism ; Systematics. Morphology. Development cycle. Physiology</subject><ispartof>FEMS microbiology letters, 1999-08, Vol.177 (1), p.109-116</ispartof><rights>1999 Federation of European Microbiological Societies. Published by Elsevier Science B.V. 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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.</description><subject>Ammonium</subject><subject>Ammonium phosphates</subject><subject>Biological and medical sciences</subject><subject>Biosynthesis</subject><subject>Carbon/nitrogen ratio</subject><subject>Carboxylic Acids - metabolism</subject><subject>Corn</subject><subject>Culture Media</subject><subject>Food contamination</subject><subject>Fumonisin</subject><subject>Fumonisin B1</subject><subject>Fumonisins</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fungal plant pathogens</subject><subject>Fungi</subject><subject>Fusarium moniliforme</subject><subject>Gibberella - drug effects</subject><subject>Gibberella - growth &amp; development</subject><subject>Gibberella - metabolism</subject><subject>Gibberella fujikuroi</subject><subject>Inoculum</subject><subject>Kinetics</subject><subject>Metabolites</subject><subject>Microbiology</subject><subject>Mycelia</subject><subject>Mycology</subject><subject>Mycotoxin</subject><subject>Mycotoxins</subject><subject>Mycotoxins - biosynthesis</subject><subject>Nitrogen</subject><subject>Nitrogen - metabolism</subject><subject>Nitrogen metabolite repression</subject><subject>Pathogenicity, host-agent relations, miscellaneous strains, epidemiology</subject><subject>Phosphates - metabolism</subject><subject>Phosphates - pharmacology</subject><subject>Phytopathology. Animal pests. Plant and forest protection</subject><subject>plant pathogenic fungi</subject><subject>Regulatory sequences</subject><subject>Risk reduction</subject><subject>Sucrose - metabolism</subject><subject>Systematics. Morphology. Development cycle. 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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.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>10436928</pmid><doi>10.1111/j.1574-6968.1999.tb13720.x</doi><tpages>8</tpages></addata></record>
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identifier ISSN: 0378-1097
ispartof FEMS microbiology letters, 1999-08, Vol.177 (1), p.109-116
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subjects Ammonium
Ammonium phosphates
Biological and medical sciences
Biosynthesis
Carbon/nitrogen ratio
Carboxylic Acids - metabolism
Corn
Culture Media
Food contamination
Fumonisin
Fumonisin B1
Fumonisins
Fundamental and applied biological sciences. Psychology
Fungal plant pathogens
Fungi
Fusarium moniliforme
Gibberella - drug effects
Gibberella - growth & development
Gibberella - metabolism
Gibberella fujikuroi
Inoculum
Kinetics
Metabolites
Microbiology
Mycelia
Mycology
Mycotoxin
Mycotoxins
Mycotoxins - biosynthesis
Nitrogen
Nitrogen - metabolism
Nitrogen metabolite repression
Pathogenicity, host-agent relations, miscellaneous strains, epidemiology
Phosphates - metabolism
Phosphates - pharmacology
Phytopathology. Animal pests. Plant and forest protection
plant pathogenic fungi
Regulatory sequences
Risk reduction
Sucrose - metabolism
Systematics. Morphology. Development cycle. Physiology
title Nitrogen repression of fumonisin B1 biosynthesis in Gibberella fujikuroi
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