Dipartimento di Biologia Vegetable, Universitá "La Sapienza", Largo Cristina di Svezia 24, 00165, Roma, Italy.
Mycotoxin Res. 2006 Mar;22(1):39-47. doi: 10.1007/BF02954556.
A close correlation between lipoperoxide formation in cells ofAspergillus parasiticus and aflatoxin biosynthesis has been established in rich and poor media in which oxidative stress was induced by addition of cumene hydroperoxide, a lipoperoxidation inducer. The presence of hydroperoxides of linoleic acid inA. parasiticus mycelia was analysed by liquid chromatography-mass spectrometry (LC-MS). This relation appears to be driven by activation of certain oxidative stress related transcription factors, such asyap1-like,skn7-like andhsf2-like. Activation of these factors then leads to the promotion of transcription of genes encoding antioxidant-related enzymes, such as superoxide dismutase, catalase and glutathione peroxidase.The incomplete seavenging of intracellular oxidation inA. parasiticus cells can lead to aflatoxin biosynthesis. The relationship between oxidative stress and aflatoxin biosynthesis is indicated by the high correlation among increased activity of lipoperoxidation and the antioxidant defence system with formation of aflatoxins.With regard to the relationship of oxidative stress and aflatoxin biosynthesis, the mechanism of action of butylated hydroxyl anisole (BHA), an antioxidant compound, in the control of aflatoxin biosynthesis was also investigated. Results indicate this compound can act,per se, by inhibiting lipoperoxidation and by inducing antioxidative defence responses of the fungal cell.
在富营养和贫营养培养基中,通过添加脂氢过氧化物(一种脂过氧化诱导剂)诱导氧化应激,已确立细胞中脂过氧化物的形成与黄曲霉菌产黄曲霉毒素之间的密切相关性。通过液相色谱-质谱(LC-MS)分析了黄曲霉菌丝体中亚油酸的过氧化物。这种关系似乎是由某些与氧化应激相关的转录因子的激活驱动的,如 yap1 样、skn7 样和 hsf2 样。这些因子的激活导致编码抗氧化相关酶的基因转录的促进,如超氧化物歧化酶、过氧化氢酶和谷胱甘肽过氧化物酶。黄曲霉菌细胞内氧化的不完全清除会导致黄曲霉毒素的生物合成。氧化应激与黄曲霉毒素生物合成之间的关系表明,脂过氧化和抗氧化防御系统活性的增加与黄曲霉毒素的形成之间存在高度相关性。关于氧化应激与黄曲霉毒素生物合成的关系,还研究了抗氧化化合物丁基羟基茴香醚(BHA)在控制黄曲霉毒素生物合成中的作用机制。结果表明,该化合物本身可以通过抑制脂过氧化和诱导真菌细胞的抗氧化防御反应来发挥作用。