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Inhibitory Activities of Blasticidin S Derivatives on Aflatoxin Production by Aspergillus Flavus

机译:弹性蛋白S衍生物对黄曲霉产生黄曲霉毒素的抑制活性

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摘要

Blasticidin S (BcS) is a protein synthesis inhibitor which shows strong growth inhibitory activity against a number of microorganisms. However, BcS inhibited aflatoxin production by Aspergillus flavus without affecting its growth. In order to obtain information about the structure–activity relationship of BcS as an aflatoxin production inhibitor, BcS derivatives were prepared and their aflatoxin production inhibitory activities were evaluated. Among five derivatives, blasticidin S carboxymethyl ester, deaminohydroxyblasticidin S, and pyrimidinoblasticidin S showed inhibitory activity, while the others did not. The IC50 value for aflatoxin production of the carboxymethyl ester derivative was one-fifth of that of BcS although their antimicrobial activities were almost the same. These results indicate that the inhibitory activity of BcS against aflatoxin production was enhanced by esterification of its carboxyl group and that the carboxymethyl ester derivative might be more suitable for practical use than BcS because of the specificity of the carboxymethyl ester derivative, which inhibited aflatoxin production more than BcS.
机译:弹性蛋白S(BcS)是一种蛋白质合成抑制剂,对多种微生物显示出强大的生长抑制活性。但是,BcS抑制了黄曲霉产生黄曲霉毒素而不影响其生长。为了获得有关作为黄曲霉毒素生产抑制剂的BcS的构效关系的信息,制备了BcS衍生物并评估了其对黄曲霉毒素生产的抑制活性。在五种衍生物中,杀稻瘟菌素S羧甲基酯,脱氨基羟基杀稻瘟素S和嘧啶菌杀稻瘟素S具有抑制活性,而其他的则没有抑制活性。羧甲基酯衍生物的黄曲霉毒素生产的IC50值是BcS的五分之一,尽管它们的抗菌活性几乎相同。这些结果表明,通过其羧基的酯化增强了BcS对黄曲霉毒素产生的抑制活性,并且由于羧甲基酯衍生物的特异性,羧甲基酯衍生物可能比BcS更适合于实际使用,从而更抑制了黄曲霉毒素的产生。比BCS。

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