College of Bioengineering, Henan University of Technology, Zhengzhou 450001, China.
Henan Provincial Key Laboratory of Biological Processing and Nutritional Function of Wheat, Zhengzhou 450001, China.
Toxins (Basel). 2022 Aug 12;14(8):551. doi: 10.3390/toxins14080551.
produces carcinogenic ochratoxin A (OTA), a serious food safety and human health concern. Here, the ability of CBS 513.88 to produce OTA using different carbon sources was investigated and the underlying regulatory mechanism was elucidated. The results indicated that 6% sucrose, glucose, and arabinose could trigger OTA biosynthesis and that 1586 differentially expressed genes (DEGs) overlapped compared to a non-inducing nutritional source, peptone. The genes that participated in OTA and its precursor phenylalanine biosynthesis, including , , , , and , were up-regulated, while the genes involved in oxidant detoxification, such as and , were down-regulated. Correspondingly, the activities of catalase and peroxidase were also decreased. Notably, the novel -like transcription factor An12g00840 (), which is vital in regulating OTA biosynthesis, was identified. Deletion of elevated the OTA yields by 47.65%, 54.60%, and 309.23% using sucrose, glucose, and arabinose as carbon sources, respectively. Additionally, deletion of increased the superoxide anion and HO contents, as well as the sensitivity to HO, using the three carbon sources. These results suggest that these three carbon sources repressed , leading to the up-regulation of the OTA biosynthetic genes and alteration of cellular redox homeostasis, ultimately triggering OTA biosynthesis in .
产生致癌的赭曲霉毒素 A(OTA),这是一个严重的食品安全和人类健康问题。在这里,研究了 CBS 513.88 使用不同碳源产生 OTA 的能力,并阐明了其潜在的调控机制。结果表明,6%的蔗糖、葡萄糖和阿拉伯糖可以触发 OTA 的生物合成,与非诱导营养源蛋白胨相比,有 1586 个差异表达基因(DEGs)重叠。参与 OTA 和其前体苯丙氨酸生物合成的基因,包括、、、、和,上调,而参与氧化应激解毒的基因,如和,下调。相应地,过氧化氢酶和过氧化物酶的活性也降低了。值得注意的是,鉴定了一种新型的转录因子 An12g00840(),它在调节 OTA 生物合成中起着至关重要的作用。使用蔗糖、葡萄糖和阿拉伯糖作为碳源时,缺失会分别使 OTA 的产量提高 47.65%、54.60%和 309.23%。此外,缺失会增加三种碳源的超氧阴离子和 HO 含量,以及对 HO 的敏感性。这些结果表明,这三种碳源抑制了,导致 OTA 生物合成基因的上调和细胞氧化还原稳态的改变,最终触发了 CBS 513.88 中的 OTA 生物合成。