Metabolic and Biomolecular Engineering National Research Laboratory, Department of Chemical and Biomolecular Engineering (BK21 Plus Program), Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141, Republic of Korea; Institute for the BioCentury, KAIST, Daejeon 34141, Republic of Korea.
Metabolic and Biomolecular Engineering National Research Laboratory, Department of Chemical and Biomolecular Engineering (BK21 Plus Program), Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141, Republic of Korea; BioProcess Engineering Research Center and Bioinformatics Research Center, KAIST, Daejeon 34141, Republic of Korea; Institute for the BioCentury, KAIST, Daejeon 34141, Republic of Korea.
Cell Syst. 2017 Oct 25;5(4):418-426.e4. doi: 10.1016/j.cels.2017.08.016. Epub 2017 Sep 27.
Escherichia coli gene expression knockdown using synthetic small RNA (sRNA) can be fine-tuned by altering sRNA sequences to modulate target mRNA-binding ability, but this requires thorough checking for off-target effects. Here, we present an sRNA gene expression knockdown system fine-tuned by using different promoters to modulate synthetic sRNA abundance. Our approach entails selecting knockdown target genes resulting from in silico flux response analysis and those related to product biosynthesis then screening strains transformed with a library of synthetic sRNA-promoter combinations for enhanced production. We engineered two E. coli strains, both utilizing fine-tuned repression of argF and glnA through our approach; one produced putrescine (42.3 ± 1.0 g/L) and the other L-proline (33.8 ± 1.6 g/L) by fed-batch culture. Fine-tuned gene knockdown by controlling sRNA abundance will be useful for rapid design of microbial strains through simultaneously optimizing expression of multiple genes at a systems level, as it overcomes the difficulties of constructing and testing many different sRNAs and checking their cross-reactivity.
利用合成小 RNA(sRNA)对大肠杆菌基因表达进行敲低,可以通过改变 sRNA 序列来精细调节靶 mRNA 结合能力,但这需要彻底检查脱靶效应。在这里,我们提出了一种通过使用不同启动子来调节合成 sRNA 丰度的 sRNA 基因表达敲低系统。我们的方法包括选择基于计算机通量响应分析的敲低靶基因和与产物生物合成相关的基因,然后筛选转化有合成 sRNA-启动子组合文库的菌株,以提高产量。我们构建了两种大肠杆菌菌株,都通过我们的方法精细调节了 argF 和 glnA 的抑制;一种通过分批补料培养生产腐胺(42.3±1.0 g/L),另一种生产 L-脯氨酸(33.8±1.6 g/L)。通过控制 sRNA 丰度进行精细的基因敲低,将有助于通过在系统水平上同时优化多个基因的表达来快速设计微生物菌株,因为它克服了构建和测试许多不同 sRNA 并检查它们的交叉反应性的困难。