Payne G A, Nystrom G J, Bhatnagar D, Cleveland T E, Woloshuk C P
Department of Plant Pathology, North Carolina State University, Raleigh, 27695-7616.
Appl Environ Microbiol. 1993 Jan;59(1):156-62. doi: 10.1128/aem.59.1.156-162.1993.
Aflatoxins are extremely potent carcinogens produced by Aspergillus flavus and Aspergillus parasiticus. Cloning of genes in the aflatoxin pathway provides a specific approach to understanding the regulation of aflatoxin biosynthesis and, subsequently, to the control of aflatoxin contamination of food and feed. This paper reports the isolation of a gene involved in aflatoxin biosynthesis by complementation of an aflatoxin-nonproducing mutant with a wild-type genomic cosmid library of A. flavus. Strain 650-33, blocked in aflatoxin biosynthesis at the afl-2 allele, was complemented by a 32-kb cosmid clone (B9), resulting in the production of aflatoxin. The onset and profile of aflatoxin accumulation was similar for the transformed strain and the wild-type strain (NRRL 3357) of the fungus, indicating that the integrated gene is under the same control as in wild-type strains. Complementation analyses with DNA fragments from B9 indicated that the gene resides within a 2.2-kb fragment. Because this gene complements the mutated afl-2 allele, it was designated afl-2. Genetic evidence obtained from a double mutant showed that afl-2 is involved in aflatoxin biosynthesis before the formation of norsolorinic acid, the first stable intermediate identified in the pathway. Further, metabolite feeding studies with the mutant, transformed, and wild-type cultures and enzymatic activity measurements in cell extracts of these cultures suggest that afl-2 regulates gene expression or the activity of other aflatoxin pathway enzymes. This is the first reported isolation of a gene for aflatoxin biosynthesis in A. flavus.
黄曲霉毒素是由黄曲霉和寄生曲霉产生的极具毒性的致癌物。克隆黄曲霉毒素合成途径中的基因,为理解黄曲霉毒素生物合成的调控机制以及随后控制食品和饲料中的黄曲霉毒素污染提供了一种特定方法。本文报道了通过用黄曲霉野生型基因组黏粒文库对黄曲霉毒素非产生突变体进行互补,从而分离出一个参与黄曲霉毒素生物合成的基因。在 afl-2 等位基因处阻断黄曲霉毒素生物合成的菌株 650-33,被一个 32 kb 的黏粒克隆(B9)互补,从而产生了黄曲霉毒素。转化菌株和该真菌的野生型菌株(NRRL 3357)中黄曲霉毒素积累的起始和模式相似,这表明整合的基因与野生型菌株受相同的调控。用来自 B9 的 DNA 片段进行的互补分析表明,该基因位于一个 2.2 kb 的片段内。由于该基因互补了突变的 afl-2 等位基因,因此将其命名为 afl-2。从双突变体获得的遗传证据表明,afl-2 在途径中第一个被鉴定出的稳定中间体——降索尔酸形成之前就参与了黄曲霉毒素的生物合成。此外,对突变体、转化体和野生型培养物进行的代谢物饲喂研究以及对这些培养物细胞提取物中的酶活性测量表明,afl-2 调节基因表达或其他黄曲霉毒素途径酶的活性。这是首次报道在黄曲霉中分离出黄曲霉毒素生物合成基因。