Appl Environ Microbiol. 1997 Oct;63(10):3995-4000. doi: 10.1128/aem.63.10.3995-4000.1997.
The aflatoxin biosynthetic pathway regulatory gene, aflR, encodes a putative 47-kDa protein containing a zinc cluster DNA binding motif. It is required for the transcription of all of the characterized aflatoxin pathway genes in both Aspergillus flavus and Aspergillus parasiticus. The objective of this study was to examine the effects of aflR overexpression on temporal gene expression, aflatoxin production, and nitrate inhibition of aflatoxin biosynthesis in A. flavus. An inducible expression construct was made by fusing the coding region of aflR to the promoter region of the A. flavus adh1 gene. This construct was transformed into A. flavus 656-2 (FGSC A1010), a strain mutated at the aflR locus. Strain 656-2 containing the adh1(p)::aflR construct had induced transcription of two early aflatoxin pathway genes, nor-1 and pksA, and produced wild-type concentrations of aflatoxin in a temporal pattern similar to that of wild-type strains of A. flavus. Strains 656-2 and 86-10 (FGSC A1009) an aflatoxigenic strain, were transformed with a construct containing the constitutive promoter gpdA driving aflR. Transformants of these strains constitutively expressed aflR, fas-1A, pksA, nor-1, and omtA but did not constitutively produce aflatoxin. Strain 86-10 containing the gpdA(p)::aflR construct produced 50 times more aflatoxin than 86-10, but the temporal pattern of aflatoxin production was the same as for 86-10, and aflatoxin production was also induced by sucrose. The addition of 10 g of nitrate per liter to sucrose low salts medium inhibited aflatoxin production by both strain 86-10 and a transformant of 86-10 containing the gpdA(p)::aflR construct, indicating that nitrate inhibition of aflatoxin biosynthesis does not occur solely at the level of aflR transcription. These studies show that constitutive overexpression of the pathway transcriptional regulatory gene aflR leads to higher transcript accumulation of pathway genes and increased aflatoxin production but that the initiation of aflatoxin biosynthesis is not solely regulated by the transcriptional activities of the biosynthetic pathway.
黄曲霉毒素生物合成途径调控基因 aflR 编码一个假定的 47kDa 蛋白,含有锌簇 DNA 结合基序。它是曲霉属黄曲霉和寄生曲霉中所有特征化的黄曲霉毒素途径基因转录所必需的。本研究的目的是研究 aflR 过表达对黄曲霉时空基因表达、黄曲霉毒素产生和硝酸盐抑制黄曲霉毒素生物合成的影响。通过将 aflR 的编码区与黄曲霉 adh1 基因的启动子区域融合,构建了一个可诱导表达的构建体。该构建体转化到 aflR 基因座突变的黄曲霉 656-2(FGSC A1010)菌株中。含有 adh1(p)::aflR 构建体的 656-2 菌株诱导了两个早期黄曲霉毒素途径基因 nor-1 和 pksA 的转录,并以类似于野生型黄曲霉菌株的时空模式产生了野生型浓度的黄曲霉毒素。菌株 656-2 和 86-10(FGSC A1009)是一个产黄曲霉毒素的菌株,用含有组成型启动子 gpdA 驱动 aflR 的构建体转化。这些菌株的转化体组成性表达 aflR、fas-1A、pksA、nor-1 和 omtA,但不组成性地产生黄曲霉毒素。含有 gpdA(p)::aflR 构建体的 86-10 菌株产生的黄曲霉毒素比 86-10 菌株多 50 倍,但黄曲霉毒素产生的时空模式与 86-10 菌株相同,蔗糖也能诱导黄曲霉毒素的产生。在蔗糖低盐培养基中添加 10g/L 的硝酸盐抑制了 86-10 菌株和含有 gpdA(p)::aflR 构建体的 86-10 转化株的黄曲霉毒素产生,表明硝酸盐抑制黄曲霉毒素生物合成不仅发生在 aflR 转录水平上。这些研究表明,途径转录调控基因 aflR 的组成性过表达导致途径基因的转录物积累增加,黄曲霉毒素产量增加,但黄曲霉毒素生物合成的起始并不完全受生物合成途径的转录活性调节。