Bioelectrochemical system achieves a 63-fold increase in pyruvic acid production rate, suggesting a route for green synthesis from biomass.
The enzymatic synthesis of pyruvic acid (PyA) from biomass‐derived lactic acid (LA) using oxidases under mild conditions represents a promising sustainable route. However, its efficiency is hindered by insufficient O 2 mass transfer and undesired PyA degradation resulting from the enzymatic byproduct H 2 O 2 . Herein, we present an gas‐liquid‐solid triphase bioelectrochemical reaction system that can address these two challenges symmetrically. This design ensures an efficient supply of O 2 from the air phase to the lactate oxidase (LOx) active zone, thereby overcoming the mass‐transfer constraint of oxygen. Simultaneously, the in situ electro‐oxidation of H 2 O 2 minimizes the degradation of PyA. Consequently, the reaction system achieves a production rate of 54.34 µM h −1 U −1 , which is 63‐fold greater than that of conventional liquid‐solid diphase enzymatic systems. Mathematical modeling and electrochemical studies revealed that enhanced local O 2 levels and efficient H 2 O 2 removal are the keys to superior performance. This work provides a sustainable and efficient route for PyA biosynthesis while demonstrating the potential of engineered bioelectrocatalytic environments for green synthesis.
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Huang et al. (2026) studied this question.
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