Valcarcel R, Bennett J W, Vitanza J
Mycopathologia. 1986 Apr;94(1):7-10. doi: 10.1007/BF00437255.
We have treated a wild type strain of Aspergillus parasiticus with several known aflatoxin inhibitors in hopes of finding specific metabolic blocks in the aflatoxin biosynthetic pathway. In defined medium, benzoic acid (2 and 3 mg/ml), cinnamon (1 mg/ml), and sodium acetate (5 mg/ml) were fungitoxic. Benzoic acid (0.5 and 1 mg/ml), chlorox (5 microliters/ml), and dimethyl sulfoxide (5 microliters/ml) did not affect dry weight or mycelial pigmentation. Sodium benzoate (1, 2, 4 and 8 mg/ml) added after 2 days growth inhibited aflatoxin production in two defined media. We were unable to confirm previously published reports that an uncharacterized yellow pigment accumulates with benzoate-inhibition of aflatoxin biosynthesis.
我们用几种已知的黄曲霉毒素抑制剂处理了寄生曲霉的野生型菌株,希望能在黄曲霉毒素生物合成途径中找到特定的代谢阻断点。在限定培养基中,苯甲酸(2和3毫克/毫升)、肉桂(1毫克/毫升)和醋酸钠(5毫克/毫升)具有真菌毒性。苯甲酸(0.5和1毫克/毫升)、含氯消毒剂(5微升/毫升)和二甲基亚砜(5微升/毫升)不影响干重或菌丝色素沉着。在生长2天后添加苯甲酸钠(1、2、4和8毫克/毫升)可抑制两种限定培养基中的黄曲霉毒素产生。我们无法证实之前发表的报告,即苯甲酸抑制黄曲霉毒素生物合成时会积累一种未鉴定的黄色色素。