Shandong Provincial Key Laboratory of Synthetic Biology, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, Qingdao, Shandong, 266101, China; Shandong Energy Institute, Qingdao, Shandong, 266101, China; Qingdao New Energy Shandong Laboratory, Qingdao, Shandong, 266101, China; University of Chinese Academy of Sciences, Beijing, 100049, China.
Shandong Provincial Key Laboratory of Synthetic Biology, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, Qingdao, Shandong, 266101, China; Shandong Energy Institute, Qingdao, Shandong, 266101, China; Qingdao New Energy Shandong Laboratory, Qingdao, Shandong, 266101, China.
Metab Eng. 2022 Nov;74:130-138. doi: 10.1016/j.ymben.2022.10.007. Epub 2022 Nov 1.
Physcion is a characteristic component of the traditional herb rhubarb with diverse pharmacological activities that has been commercially approved as an herbal fungicide. Nevertheless, its extremely low contents, costly purification procedure and geographically restricted planting severely hinder its application. Here, a cell factory was constructed in the filamentous fungus Aspergillus terreus for physcion production via microbial fermentation by integrating a pathway-modified emodin accumulation module and a position-selective emodin methylation module. Specifically, 1.71 g/L emodin accumulated when the transcriptional activator GedR and the emodin-1-OH-O-methyltransferase GedA in the geodin biosynthetic pathway were overexpressed and knocked out, respectively. Subsequently, potential emodin-3-OH-O-methyltransferase candidates were enzymatically screened in vitro and introduced into the emodin-accumulating mutant in vivo to generate a physcion-producing strain showing the highest titre of 6.3 g/L in fed-batch fermentation. Thus, our study provides an alternative strategy for the highly efficient, economical production of physcion and a representative example for microbial synthetic biology.
大黄素是传统草药大黄的特征成分,具有多种药理活性,已被商业批准为草药杀菌剂。然而,其含量极低、纯化工艺昂贵且种植地域受限,严重阻碍了其应用。在这里,通过微生物发酵,在丝状真菌土曲霉中构建了一个细胞工厂,用于通过整合途径修饰的大黄素积累模块和位置选择性大黄素甲基化模块来生产大黄素。具体而言,当在大黄素生物合成途径中过表达转录激活因子 GedR 和大黄素-1-OH-O-甲基转移酶 GedA 并分别敲除时,可积累 1.71g/L 的大黄素。随后,在体外对潜在的大黄素-3-OH-O-甲基转移酶候选物进行酶筛选,并将其引入大黄素积累突变体中,在分批补料发酵中产生了最高产量为 6.3g/L 的大黄素产生菌株。因此,本研究为大黄素的高效、经济生产提供了一种替代策略,也是微生物合成生物学的一个代表性例子。