Li Qinghua, Lu Jinchang, Liu Jingya, Li Jianghua, Zhang Guoqiang, Du Guocheng, Chen Jian
Science Center for Future Foods, Jiangnan University, 1800 Lihu Road, Wuxi, 214122, Jiangsu, China.
National Engineering Research Center for Cereal Fermentation and Food Biomanufacturing, Jiangnan University, 1800 Lihu Road, Wuxi, 214122, Jiangsu, China.
Biotechnol Biofuels Bioprod. 2023 Nov 29;16(1):185. doi: 10.1186/s13068-023-02437-6.
The exceptional protein secretion capacity, intricate post-translational modification processes, and inherent safety features of A. oryzae make it a promising expression system. However, heterologous protein expression levels of existing A. oryzae species cannot meet the requirement for industrial-scale production. Therefore, establishing an efficient screening technology is significant for the development of the A. oryzae expression system.
In this work, a high-throughput screening method suitable for A. oryzae has been established by combining the microfluidic system and flow cytometry. Its screening efficiency can reach 350 droplets per minute. The diameter of the microdroplet was enlarged to 290 µm to adapt to the polar growth of A. oryzae hyphae. Through enrichment and screening from approximately 450,000 droplets within 2 weeks, a high-producing strain with α-amylase increased by 6.6 times was successfully obtained. Furthermore, 29 mutated genes were identified by genome resequencing of high-yield strains, with 15 genes subjected to editing and validation. Two genes may individually influence α-amylase expression in A. oryzae by affecting membrane-associated multicellular processes and regulating the transcription of related genes.
The developed high-throughput screening strategy provides a reference for other filamentous fungi and Streptomyces. Besides, the strains with different excellent characteristics obtained by efficient screening can also provide materials for the analysis of genetic and regulatory mechanisms in the A. oryzae expression system.
米曲霉卓越的蛋白质分泌能力、复杂的翻译后修饰过程以及固有的安全特性使其成为一个有前景的表达系统。然而,现有米曲霉菌种的异源蛋白表达水平无法满足工业规模生产的需求。因此,建立高效的筛选技术对米曲霉表达系统的发展具有重要意义。
在本研究中,通过将微流控系统与流式细胞术相结合,建立了一种适用于米曲霉的高通量筛选方法。其筛选效率可达每分钟350个液滴。将微滴直径扩大到290 µm以适应米曲霉菌丝的极性生长。通过在2周内从约450,000个液滴中进行富集和筛选,成功获得了一株α淀粉酶产量提高6.6倍的高产菌株。此外,通过对高产菌株的基因组重测序鉴定出29个突变基因,其中15个基因进行了编辑和验证。两个基因可能分别通过影响膜相关的多细胞过程和调节相关基因的转录来影响米曲霉中α淀粉酶的表达。
所开发的高通量筛选策略为其他丝状真菌和链霉菌提供了参考。此外,通过高效筛选获得的具有不同优良特性的菌株也可为米曲霉表达系统中遗传和调控机制的分析提供材料。