Shima Yoko, Shiina Marisa, Shinozawa Takao, Ito Yasuhiro, Nakajima Hiromitsu, Adachi Yoshikazu, Yabe Kimiko
National Food Research Institute, National Agriculture and Food Research Organization (NARO), Tsukuba, Ibaraki, Japan.
Fungal Genet Biol. 2009 Mar;46(3):221-31. doi: 10.1016/j.fgb.2008.12.005. Epub 2009 Jan 3.
Three reactions from hydroxyversicolorone to versicolorone, from versiconal hemiacetal acetate to versiconol acetate, and from versiconal to versiconol are involved in a metabolic grid in aflatoxin biosynthesis. This work demonstrated that the same reductase of Aspergillus parasiticus catalyzes the three reactions. The gene (named vrdA) encoding the reductase was cloned, and its sequence did not show homology to any regions in aflatoxin gene cluster. Its cDNA encoding a 38,566Da protein was separated by three introns in the genome. Deletion of the vrdA gene in A. parasiticus caused a significant decrease in enzyme activity, but did not affect aflatoxin productivity of the fungi. Although the vrdA gene was expressed in culture conditions conducive to aflatoxin production, it was expressed even in the aflR deletion mutant. These results suggest that the vrdA is not an aflatoxin biosynthesis gene, although it actually participates in aflatoxin biosynthesis in cells.
在黄曲霉毒素生物合成的代谢网络中,存在从羟基杂色曲菌素到杂色曲菌素、从杂色曲酸半缩醛乙酸酯到杂色曲醇乙酸酯以及从杂色曲酸到杂色曲醇的三种反应。这项研究表明,寄生曲霉的同一种还原酶催化这三种反应。编码该还原酶的基因(命名为vrdA)被克隆,其序列与黄曲霉毒素基因簇中的任何区域均无同源性。其编码38,566Da蛋白质的cDNA在基因组中被三个内含子隔开。寄生曲霉中vrdA基因的缺失导致酶活性显著降低,但不影响真菌的黄曲霉毒素产生能力。尽管vrdA基因在有利于黄曲霉毒素产生的培养条件下表达,但它甚至在aflR缺失突变体中也有表达。这些结果表明,vrdA不是黄曲霉毒素生物合成基因,尽管它实际上在细胞中参与黄曲霉毒素的生物合成。