Guzmán-de-Peña D, Ruiz-Herrera J
Departamento de Genética, Centro de Investigación y de Estudios Avanzados del IPN, Unidad Irapuato, Guanajuato, México.
Fungal Genet Biol. 1997 Apr;21(2):198-205. doi: 10.1006/fgbi.1996.0945.
Regulation of aflatoxin biosynthesis during differentiation of Aspergillus parasiticus was analyzed by using a drug that inhibits the development of the fungus and mutants affected in sporulation. Diaminobutanone, a competitive inhibitor of ornithine decarboxylase, repressed spore germination. If added after spore germination had occurred, it blocked sporulation completely and suppressed aflatoxin biosynthesis, but was only partially inhibitory of mycelial growth. Putrescine partially counteracted the inhibitory effect of the drug on both sporulation and aflatoxin biosynthesis. Analysis of mutants affected in sporulation confirmed the existence of a relationship between sporulation and aflatoxin formation. A nonsporulating mutant was unable to synthesize aflatoxins. In a sectorial mutant, the sporulating sector synthesized aflatoxins normally, whereas the asporogenous sector was unable to do so. It is suggested that regulation of aflatoxin biosynthesis is correlated with the sporulation process.
利用一种抑制真菌发育的药物以及在孢子形成方面有缺陷的突变体,分析了寄生曲霉分化过程中黄曲霉毒素生物合成的调控情况。二氨基丁酮是鸟氨酸脱羧酶的竞争性抑制剂,它能抑制孢子萌发。如果在孢子萌发后添加,它会完全阻断孢子形成并抑制黄曲霉毒素的生物合成,但对菌丝体生长只有部分抑制作用。腐胺能部分抵消该药物对孢子形成和黄曲霉毒素生物合成的抑制作用。对孢子形成有缺陷的突变体的分析证实了孢子形成与黄曲霉毒素形成之间存在关联。一个不产孢的突变体无法合成黄曲霉毒素。在一个扇形突变体中,产孢扇形区能正常合成黄曲霉毒素,而不产孢扇形区则无法合成。研究表明,黄曲霉毒素生物合成的调控与孢子形成过程相关。