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用于 CO 还原的电-生物混合系统。

Electrical-biological hybrid system for CO reduction.

机构信息

Center for Sustainable Resource Science, RIKEN, 1-7-22, Suehiro-cho, Tsurimi-ku, Yokohama, Kanagawa 230-0045, Japan; Department of Chemistry, University of California, One Shields Ave, Davis, CA 95616, USA.

Environmental Science Research Laboratory, Central Research Institute of Electric Power Industry, 1646 Abiko, Abiko, Chiba 270-1194, Japan.

出版信息

Metab Eng. 2018 May;47:211-218. doi: 10.1016/j.ymben.2018.03.015. Epub 2018 Mar 23.

Abstract

Here we have developed an electrochemical-biological hybrid system to fix CO. Natural biological CO fixation processes are relatively slow. To increase the speed of fixation we applied electrocatalysts to reduce CO to formate. We chose a user-friendly organism, Escherichia coli, as host. Overall, the newly constructed CO and formate fixation pathway converts two formate and one CO to one pyruvate via glycine and L-serine in E. coli. First, one formate and one CO 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 CO and electricity. Results show promise for using this hybrid system for chemical production from CO and electricity.

摘要

在这里,我们开发了一种电化学-生物混合系统来固定 CO。自然的生物 CO 固定过程相对较慢。为了提高固定速度,我们应用电催化剂将 CO 还原为甲酸盐。我们选择了一种用户友好的生物体大肠杆菌作为宿主。总的来说,新构建的 CO 和甲酸盐固定途径通过大肠杆菌中的甘氨酸和 L-丝氨酸将两个甲酸盐和一个 CO 转化为一个丙酮酸。首先,一个甲酸盐和一个 CO 转化为一个甘氨酸。其次,L-丝氨酸由一个甘氨酸和一个甲酸盐产生。最后,L-丝氨酸转化为丙酮酸。大肠杆菌的遗传可操作性使我们能够平衡途径的各种参数。该途径的碳通量足以补偿该菌株中 L-丝氨酸的营养缺陷。总的来说,我们将电催化和生物系统集成到一个单一的容器中,以支持大肠杆菌利用 CO 和电力生长。结果表明,该混合系统有望用于从 CO 和电力生产化学品。

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