Key Laboratory of Carbohydrate Chemistry and Biotechnology, Ministry of Education, Jiangnan University, Wuxi, 214122, China; Key Laboratory of Industrial Biotechnology, Ministry of Education, Jiangnan University, Wuxi, 214122, China.
Key Laboratory of Carbohydrate Chemistry and Biotechnology, Ministry of Education, Jiangnan University, Wuxi, 214122, China; Key Laboratory of Industrial Biotechnology, Ministry of Education, Jiangnan University, Wuxi, 214122, China.
Metab Eng. 2019 Sep;55:131-141. doi: 10.1016/j.ymben.2019.07.001. Epub 2019 Jul 6.
N-terminal coding sequences (NCSs) of genes significantly influence gene expression at the translation level and are important for fine-tuning gene expression in bacteria, however, engineering NCSs to fine-tune metabolic pathways is challenging. Here, we developed a statistics-guided native and synthetic NCSs engineering approach to fine-tune gene expression in the industrially important microorganism Bacillus subtilis. This method is based on experimentally characterizing and statistically analyzing 96 rationally selected NCSs from B. subtilis endogenous genes. These NCSs exhibited a magnitude difference of greater than 4 orders in their ability to drive gene expression in 4 different dynamic patterns, including growth-coupled, growth-delayed, consistent expression, and inhibitory patterns. Synthetic and native NCSs were used to fine-tune expression of key enzymes, identified via pathway analysis and kinetic modeling, in the biosynthetic pathway of the useful nutraceutical N-acetylneuraminic acid (NeuAc). We observed a 3.21-fold improvement in NeuAc biosynthesis, indicating that NCSs can provide a synthetic biology toolbox to fine-tune gene expression for metabolic engineering.
基因的 N 末端编码序列(NCSs)在翻译水平上显著影响基因表达,对于细菌中基因表达的精细调控非常重要,然而,工程 NCSs 以精细调控代谢途径是具有挑战性的。在这里,我们开发了一种基于统计学的天然和合成 NCSs 工程方法,以精细调控工业上重要的微生物枯草芽孢杆菌中的基因表达。该方法基于对枯草芽孢杆菌内源基因中 96 个经过合理选择的 NCSs 的实验表征和统计分析。这些 NCSs 在 4 种不同的动态模式(包括生长偶联、生长延迟、一致表达和抑制模式)中驱动基因表达的能力差异大于 4 个数量级。通过途径分析和动力学建模,我们使用合成和天然 NCSs 来精细调控生物合成途径中关键酶的表达,这些酶是通过途径分析和动力学建模确定的。我们观察到 NeuAc 生物合成的 3.21 倍提高,表明 NCSs 可以为代谢工程提供一个精细调控基因表达的合成生物学工具箱。