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首页> 外文期刊>Applied and Environmental Microbiology >Cyclo(l-Leucyl-l-Prolyl) Produced by Achromobacter xylosoxidans Inhibits Aflatoxin Production by Aspergillus parasiticus
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Cyclo(l-Leucyl-l-Prolyl) Produced by Achromobacter xylosoxidans Inhibits Aflatoxin Production by Aspergillus parasiticus

机译:木氧化无色杆菌产生的环(1-亮氨酰-1-脯氨酰)抑制寄生曲霉产生黄曲霉毒素

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Aflatoxins are potent carcinogenic and toxic substances that are produced primarily by Aspergillus flavus and Aspergillus parasiticus. We found that a bacterium remarkably inhibited production of norsolorinic acid, a precursor of aflatoxin, by A. parasiticus. This bacterium was identified as Achromobacter xylosoxidans based on its 16S ribosomal DNA sequence and was designated A. xylosoxidans NFRI-A1. A. xylosoxidans strains commonly showed similar inhibition. The inhibitory substance(s) was excreted into the medium and was stable after heat, acid, or alkaline treatment. Although the bacterium appeared to produce several inhibitory substances, we finally succeeded in purifying a major inhibitory substance from the culture medium using Diaion HP20 column chromatography, thin-layer chromatography, and high-performance liquid chromatography. The purified inhibitory substance was identified as cyclo(l-leucyl-l-prolyl) based on physicochemical methods. The 50% inhibitory concentration for aflatoxin production by A. parasiticus SYS-4 (= NRRL2999) was 0.20 mg ml?1, as determined by the tip culture method. High concentrations (more than 6.0 mg ml?1) of cyclo(l-leucyl-l-prolyl) further inhibited fungal growth. Similar inhibitory activities were observed with cyclo(d-leucyl-d-prolyl) and cyclo(l-valyl-l-prolyl), whereas cyclo(d-prolyl-l-leucyl) and cyclo(l-prolyl-d-leucyl) showed weaker activities. Reverse transcription-PCR analyses showed that cyclo(l-leucyl-l-prolyl) repressed transcription of the aflatoxin-related genes aflR, hexB, pksL1, and dmtA. This is the first report of a cyclodipeptide that affects aflatoxin production.
机译:黄曲霉毒素是有效的致癌和有毒物质,主要由黄曲霉和寄生曲霉产生。我们发现一种细菌显着抑制了寄生曲霉产生的黄曲霉毒素的前体去甲鸟尿酸。根据其16S核糖体DNA序列,该细菌被鉴定为木氧化无色杆菌,并被命名为木氧化农杆菌NFRI-A1。木氧化木霉菌株通常显示出相似的抑制作用。抑制性物质被排到培养基中,经过加热,酸或碱处理后稳定。尽管细菌似乎会产生几种抑制物质,但我们最终成功地使用Diaion HP20柱色谱,薄层色谱和高效液相色谱从培养基中纯化出了一种主要的抑制物质。根据理化方法将纯化的抑制物质鉴定为环(1-亮氨酰-1-脯氨酰)。用尖端培养法测定,寄生寄生曲霉SYS-4产生的黄曲霉毒素的50%抑制浓度(= NRRL2999)为0.20 mg ml?1。高浓度(大于6.0 mg ml?1)的环(1-亮氨酰-1-脯氨酰基)进一步抑制了真菌的生长。观察到类似的抑制活性与环(d-亮氨酰-d-脯氨酰)和环(l-缬氨酰基-l-脯氨酰),而环(d-脯氨酰基-l-亮氨酰)和环(1-脯氨酰基-d-亮氨酰)表现出较弱的活动。逆转录-PCR分析表明,环(1-亮氨酰-1-脯氨酰)抑制了黄曲霉毒素相关基因aflR,hexB,pksL1和dmtA的转录。这是影响黄曲霉毒素生产的环二肽的首次报道。

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