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Simple screening method for molds producing intracellular mycotoxins in pure cultures.

机译:在纯培养物中产生细胞内霉菌毒素的霉菌的简单筛选方法。

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摘要

A simple screening method for molds producing the intracellular mycotoxins brevianamide A, citreoviridin, cyclopiazonic acid, luteoskyrin, penitrem A, roquefortine C, sterigmatocystin, verruculogen, viomellein, and xanthomegnin was developed. After removing an agar plug from the mold culture, the mycelium on the plug is wetted with a drop of methanol-chloroform (1:2). By this treatment the intracellular mycotoxins are extracted within seconds and transferred directly to a thin-layer chromatography plate by immediately placing the plug on the plate while the mycelium is still wet. After removal of the plug, known thin-layer chromatographic procedures are carried out. The substrate (Czapek yeast autolysate agar) and growth conditions (25 degrees C for 7 days) used by Penicillium taxonomists proved suitable for the production of the mycotoxins investigated when 60 known toxigenic isolates and 865 cultures isolated from foods and feedstuffs were tested with this screening method.
机译:开发了一种简单的霉菌筛选方法,用于生产细胞内霉菌毒素布雷维酰胺A,柑桔维京丁素,环吡唑酸,卢托斯基林,青霉烯A,乳清蛋白C,葡萄球菌毒素,Verruculogen,黄变蛋白和黄原菌素。从霉菌培养物中取出琼脂塞后,用一滴甲醇-氯仿(1:2)润湿塞上的菌丝体。通过这种处理,细胞内的真菌毒素在几秒钟内被提取出来,并通过在菌丝体仍然湿润时立即将塞子放在板上而直接转移到薄层色谱板上。取下塞子后,进行已知的薄层色谱程序。青霉分类学家使用的底物(Czapek酵母自溶琼脂)和生长条件(25摄氏度,持续7天)证明适合生产真菌毒素,当通过此筛选测试从食物和饲料中分离出的60种已知产毒分离株和865种培养物时,该菌株被研究。方法。

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