Abstract
The steady increase in atmospheric CO2 levels is a key driver of anthropogenic climate change, prompting widespread global concern. In this context, the sustainable conversion of CO2 into value-added chemicals represents an attractive route toward carbon-neutral manufacturing and green chemistry. Here, we developed a proof-of-concept hybrid microbial-enzymatic electrosynthesis system that combines microbial electrosynthesis (MES) and enzymatic electrosynthesis (EES) to convert CO2 into decanoic acid under ambient conditions, using electrical energy. In the MES module, CO2 was converted to acetate via the Wood–Ljungdahl pathway of Clostridium ljungdahlii, using H2 produced by electrochemical water splitting as the electron donor. In the downstream EES module, acetate was transformed into acetyl-CoA, which was then elongated to decanoic acid through an in vitro reversed β-oxidation (rBOX) pathway driven by bioelectrocatalytic NADH regeneration. To verify the functional coupling between the two modules, 13C isotopic labeling was employed to trace carbon flow from CO2 to acetate and further to decanoic acid, confirming that MES-derived carbon served directly as the precursor for downstream chain elongation in the EES module. Under optimized conditions, the hybrid MES-EES system produced 0.80 mM decanoic acid with 81.3% specificity. These results demonstrate the successful hybrid of MES and EES, enabling the de novo bio electrosynthesis of decanoic acid from CO2 and presenting a promising approach for coupling CO2 resource utilization with renewable electrical energy.
Recommended Citation
Y. Wang et al., "Hybrid Microbial-Enzymatic Electrosynthesis For De Novo Decanoic Acid Production From CO2," Jacs Au, vol. 6, no. 7, pp. 4118 - 4127, American Chemical Society, Jul 2026.
The definitive version is available at https://doi.org/10.1021/jacsau.6c00621
Department(s)
Chemistry
Publication Status
Open Access
Keywords and Phrases
CO2conversion; cofactor regeneration; decanoic acid; enzymatic electrosynthesis; microbial electrosynthesis
International Standard Serial Number (ISSN)
2691-3704
Document Type
Article - Journal
Document Version
Final Version
File Type
text
Language(s)
English
Rights
© 2026 American Chemical Society, All rights reserved.
Creative Commons Licensing

This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 4.0 License.
Publication Date
27 Jul 2026

Comments
National Science Foundation, Grant 2002158