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某些曲霉和青霉霉菌毒素对鼠伤寒沙门氏菌的致突变性。

Mutagenicity to Salmonella typhimurium of some Aspergillus and Penicillium mycotoxins.

作者信息

Wehner F C, Thiel P G, van Rensburg S J, Demasius I P

出版信息

Mutat Res. 1978 Nov;58(2-3):193-203. doi: 10.1016/0165-1218(78)90009-5.

Abstract

17 mycotoxins produced by various Aspergillus and Penicillium species were screened for their mutagenic activity to Salmonella typhimurium strains TA98, TA100, TA1535 and TA1537, both with and without metabolic activation. Austdiol, austocystins A and D, kojic acid and viridicatumtoxin were found to be mutagenic after metabolic activation, while austdiol was also mutagenic per se. Aflatoxin B1, sterigmatocystin and versicolorin A, which were used as positive controls were also mutagenic. No mutagenic activity was evident in the case of citrinin, cyclopiazonic acid, fumitremorgen B, griseofulvin, luteoskyrin, O-methylsterigmatocystin, mycophenolic acid, ochratoxin A, patulin, penicillic acid, secalonic acid D and TR2-toxin. A good relationship was found between the mutagenic activity, or lack of it, of most of the mycotoxins with existing data on carcinogenicity. Inadequate information on the carcinogenicity of austdiol, austocystins A and D, kojic acid and viridicatumtoxin precluded correlations with mutagenicity to S. typhimurium. The relationship between chemical structure and mutagenicity of the mycotoxins is discussed.

摘要

对由各种曲霉菌和青霉菌产生的17种霉菌毒素进行了筛选,检测它们对鼠伤寒沙门氏菌TA98、TA100、TA1535和TA1537菌株的诱变活性,检测条件包括有无代谢活化。发现奥斯特二醇、奥斯特囊肿素A和D、曲酸和绿胶霉素在代谢活化后具有诱变活性,而奥斯特二醇本身也具有诱变活性。用作阳性对照的黄曲霉毒素B1、杂色曲霉素和Versicolorin A也具有诱变活性。在桔霉素、环匹阿尼酸、烟曲霉震颤素B、灰黄霉素、藤黄绿菌素、O - 甲基杂色曲霉素、霉酚酸、赭曲霉毒素A、展青霉素、青霉酸、secalonic酸D和TR2 - 毒素的情况下,未发现明显的诱变活性。发现大多数霉菌毒素的诱变活性(或无诱变活性)与现有的致癌性数据之间存在良好的关系。关于奥斯特二醇、奥斯特囊肿素A和D、曲酸和绿胶霉素致癌性的信息不足,无法将其与对鼠伤寒沙门氏菌的诱变性进行关联。讨论了霉菌毒素的化学结构与诱变性之间的关系。

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