格式化
甘氨酸
丝氨酸
大肠杆菌
营养不良
化学
固碳
生物化学
组合化学
氨基酸
磷酸化
基因
催化作用
光合作用
作者
Yohei Tashiro,Shin-ichi Hirano,Morgan M. Matson,Shota Atsumi,Akihiko Kondo
标识
DOI:10.1016/j.ymben.2018.03.015
摘要
Here we have developed an electrochemical-biological hybrid system to fix CO2. Natural biological CO2 fixation processes are relatively slow. To increase the speed of fixation we applied electrocatalysts to reduce CO2 to formate. We chose a user-friendly organism, Escherichia coli, as host. Overall, the newly constructed CO2 and formate fixation pathway converts two formate and one CO2 to one pyruvate via glycine and L-serine in E. coli. First, one formate and one CO2 are converted to one glycine. Second, L-serine is produced from one glycine and one formate. Lastly, L-serine is converted to pyruvate. E. coli's genetic tractability allowed us to balance various parameters of the pathway. The carbon flux of the pathway was sufficient to compensate L-serine auxotrophy in the strain. In total, we integrated both electrocatalysis and biological systems into a single pot to support E. coli growth with CO2 and electricity. Results show promise for using this hybrid system for chemical production from CO2 and electricity.
科研通智能强力驱动
Strongly Powered by AbleSci AI