Liu Lina, Duan Xuguo, Wu Jing
State Key Laboratory of Food Science and Technology, Jiangnan University, 1800 Lihu Avenue, Wuxi, 214122, China; School of Biotechnology and Key Laboratory of Industrial Biotechnology Ministry of Education, Jiangnan University, 1800 Lihu Avenue, Wuxi, 214122, China.
J Biotechnol. 2016 Aug 10;231:141-148. doi: 10.1016/j.jbiotec.2016.06.008. Epub 2016 Jun 11.
The fructose repressor (FruR) affects carbon flux through the central metabolic pathways of Escherichia coli. In this study, l-tryptophan production in Escherichia coli FB-04 was improved by knocking out the fruR gene, thereby inactivating FruR. This fruR knockout strain, E. coli FB-04(ΔfruR), not only exhibited higher growth efficiency, it also showed substantially improved l-tryptophan production. l-tryptophan production by E. coli FB-04(ΔfruR) and l-tryptophan yield per glucose were increased by 62.5% and 52.4%, respectively, compared with the parent E. coli FB-04. Metabolomics analysis showed that the fruR knockout significantly enhances metabolic flow through glycolysis, the pentose phosphate pathway and the TCA cycle, increasing levels of critical precursors and substrates for l-tryptophan biosynthesis. These results indicate that fruR deletion should enhance l-tryptophan production and improve the efficiency of carbon source utilization independent of genetic background.
果糖阻遏物(FruR)影响大肠杆菌中心代谢途径中的碳通量。在本研究中,通过敲除fruR基因使FruR失活,提高了大肠杆菌FB - 04中l - 色氨酸的产量。这种敲除fruR基因的菌株,即大肠杆菌FB - 04(ΔfruR),不仅表现出更高的生长效率,其l - 色氨酸产量也显著提高。与亲本大肠杆菌FB - 04相比,大肠杆菌FB - 04(ΔfruR)的l - 色氨酸产量和每葡萄糖的l - 色氨酸产率分别提高了62.5%和52.4%。代谢组学分析表明,敲除fruR显著增强了通过糖酵解、磷酸戊糖途径和三羧酸循环的代谢流,增加了l - 色氨酸生物合成关键前体和底物的水平。这些结果表明,删除fruR应能提高l - 色氨酸产量并提高碳源利用效率,且与遗传背景无关。