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首页> 外文期刊>Applied and Environmental Microbiology >Inhibition of aflatoxin biosynthesis by tolnaftate.
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Inhibition of aflatoxin biosynthesis by tolnaftate.

机译:甲苯磺酸盐对黄曲霉毒素生物合成的抑制作用。

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摘要

Tolnaftate [2-napthyl-N-methyl-N-(m-tolyl)thionocarbamate], an antifungal drug, is widely used to control superficial fungal infections in humans and other animals. In this study the effect of tolnaftate on aflatoxin biosynthesis by Aspergillus parasiticus NRRL 3240 was investigated. Tolnaftate changed the morphology of A. parasiticus to yeastlike forms and inhibited aflatoxin formation. The formation of aflatoxin G was blocked considerably, indicating a metabolic block in the conversion of aflatoxin B to aflatoxin G. The incorporation of [1-14C]acetate into aflatoxin was significantly inhibited at a concentration of 1 mM tolnaftate. The presence of zinc in the resuspension buffer resulted in reversal of the tolnaftate-induced inhibition of aflatoxin G1 biosynthesis.
机译:甲苯磺酸酯[2-萘基-N-甲基-N-(间甲苯基)硫代氨基甲酸酯]是一种抗真菌药,被广泛用于控制人类和其他动物的浅表真菌感染。在这项研究中,研究了托拉夫特对寄生曲霉NRRL 3240合成黄曲霉毒素的影响。 Tolnaftate将寄生曲霉的形态改变为酵母样形式,并抑制了黄曲霉毒素的形成。黄曲霉毒素G的形成被显着阻断,表明在黄曲霉毒素B转化为黄曲霉毒素G的代谢中受到阻滞。[1-14C]乙酸酯混入黄曲霉毒素中的浓度在1 mM甲苯磺酸盐中被显着抑制。重悬缓冲液中锌的存在导致甲苯磺酸盐诱导的黄曲霉毒素G1生物合成抑制作用的逆转。

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