Wong J J, Singh R, Hsieh D P
Mutat Res. 1977 Sep;44(3):447-50. doi: 10.1016/0027-5107(77)90102-6.
Fungal metabolites identified as the intermediates in aflatoxin biosynthetic pathway were screened for their mutagenic activity to Salmonella typhimurium TA98. Norsolorinic acid, averufin, and versiconal acetate were found to possess questionable mutagenic activity, but versicolorin A, and sterigmatocystin were significant mutagens relative to aflatoxin B1. The mutagenic activity appears to be related to the bisfuran and not the anthraquinone moiety of the molecule, even though the latter is a key structure of such potent carcinogenic mycotoxin as luteoskyrin.
对黄曲霉毒素生物合成途径中的中间产物真菌代谢物进行了鼠伤寒沙门氏菌TA98致突变活性筛选。发现诺索洛林酸、黄绿青霉素和醋酸杂色曲菌素具有可疑的致突变活性,但相对于黄曲霉毒素B1,杂色曲霉素A和柄曲霉素是显著的诱变剂。即使蒽醌部分是如黄天精这种强效致癌霉菌毒素的关键结构,但致突变活性似乎与双呋喃而非分子中的蒽醌部分有关。