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在黄曲霉毒素生物合成中,OrdA 酶催化 M-/GM-组黄曲霉毒素的产生。

Production of M-/GM-group aflatoxins catalyzed by the OrdA enzyme in aflatoxin biosynthesis.

机构信息

National Food Research Institute, National Agriculture and Food Research Organization, Tsukuba, Ibaraki 305-8642, Japan.

出版信息

Fungal Genet Biol. 2012 Sep;49(9):744-54. doi: 10.1016/j.fgb.2012.06.011. Epub 2012 Jun 30.

Abstract

Aspergillus parasiticus produces the minor aflatoxins M(1) (AFM(1)), M(2) (AFM(2)), GM(1) (AFGM(1)), and GM(2) (AFGM(2)), as well as the major aflatoxins B(1) (AFB(1)), B(2) (AFB(2)), G(1) (AFG(1)), and G(2) (AFG(2)). Feeding of A. parasiticus with aspertoxin (12c-hydroxyOMST) caused AFM(1) and AFGM(1), and cell-free experiments using the microsomal fraction of A. parasiticus and aspertoxin caused production of AFM(1), indicating that aspertoxin is a precursor of AFM(1) and AFGM(1). Feeding of the same fungus with O-methylsterigmatocystin (OMST) caused AFM(1) and AFGM(1) together with AFB(1) and AFG(1); feeding with dihydroOMST (DHOMST) caused AFM(2) and AFGM(2) together with AFB(2) and AFG(2). Incubation of either the microsomal fraction or OrdA enzyme-expressing yeast with OMST caused production of aspertoxin together with AFM(1) and AFB(1). These results demonstrated that the OrdA enzyme catalyzes both 12c-hydroxylation reaction from OMST to aspertoxin and the successive reaction from aspertoxin to AFM(1). In contrast, feeding of the fungus with AFB(1) did not produce any AFM(1), demonstrating that M-/GM-aflatoxins are not produced from B-/G-aflatoxins. Furthermore, AFM(1) together with AFB(1) and AFG(1) was also produced from 11-hydroxyOMST (HOMST) in feeding experiment of A. parasiticus, whereas no aflatoxins were produced when used the ordA deletion mutant. These results demonstrated that OrdA enzyme can also catalyze 12c-hydroxylation of HOMST to produce 11-hydroxyaspertoxin, which serves as a precursor for the production of AFM(1) and AFGM(1). The same pathway may work for the production of AFM(2) and AFGM(2) from DHOMST and dihydroHOMST through the formation of dihydroaspertoxin and dihydro-11-hydroxyaspertoxin, respectively.

摘要

寄生曲霉菌产生的次要黄曲霉毒素有 M(1)(AFM(1))、M(2)(AFM(2))、GM(1)(AFGM(1))和 GM(2)(AFGM(2)),以及主要黄曲霉毒素有 B(1)(AFB(1))、B(2)(AFB(2))、G(1)(AFG(1))和 G(2)(AFG(2))。用 Aspertoxin(12c-羟基 OMST)喂养寄生曲霉菌会导致 AFM(1)和 AFGM(1)的产生,而利用寄生曲霉菌的微粒体部分和 Aspertoxin 进行的无细胞实验导致了 AFM(1)的产生,表明 Aspertoxin 是 AFM(1)和 AFGM(1)的前体。用相同的真菌喂养 O-甲基斯特格马毒素(OMST)会导致 AFM(1)和 AFGM(1)与 AFB(1)和 AFG(1)一起产生;用二氢 OMST(DHOMST)喂养会导致 AFM(2)和 AFGM(2)与 AFB(2)和 AFG(2)一起产生。用 OMST 孵育微粒体部分或表达 OrdA 酶的酵母会导致 Aspertoxin 与 AFM(1)和 AFB(1)一起产生。这些结果表明,OrdA 酶催化 OMST 向 Aspertoxin 的 12c-羟化反应和 Aspertoxin 向 AFM(1)的连续反应。相比之下,用真菌喂养 AFB(1)不会产生任何 AFM(1),表明 M-/GM-黄曲霉毒素不是由 B-/G-黄曲霉毒素产生的。此外,在寄生曲霉菌的喂养实验中,AFM(1)与 AFB(1)和 AFG(1)也由 11-羟基 OMST(HOMST)产生,而在用 ordA 缺失突变体时则没有产生任何黄曲霉毒素。这些结果表明,OrdA 酶还可以催化 HOMST 的 12c-羟化,生成 11-羟基 Aspertoxin,作为 AFM(1)和 AFGM(1)产生的前体。同样的途径可能适用于通过形成二氢 Aspertoxin 和二氢-11-羟基 Aspertoxin,分别从 DHOMST 和二氢 HOMST 产生 AFM(2)和 AFGM(2)。

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