You are here : Home > News > An enzymatic process for reducing CO2

Découvertes et avancées | Scientific result | Bioenergy | Molecular mechanisms | Chemistry

An enzymatic process for reducing CO2


​Researchers from the CEA-Irig and their partners have developed a new enzymatic process for reducing CO2 and oxidizing CO. Efficient and able to operate under mild conditions, it could be used to purify gas from biomass pyrolysis in order to produce fuels or chemical precursors. 

Published on 6 September 2021

The conversion of biomass into synthesis gas would make it possible to exploit the energy contained in wood in the absence of any direct combustion. This process involves gasifying the organic matter by pyrolysis. The resulting mixture consists of recoverable gases (CH4 and CO), as well as numerous impurities (CO2, H2S, etc.) which must be eliminated, in particular by reduction of CO2 (to CO) or oxidation of CO (to CO2).

In this context, biocatalysts of CO2 reduction have the advantage of being highly selective and efficient under mild conditions (ambient temperature and pressure, aqueous solvents). However, they suffer from a lack of stability and the high cost of large-scale enzyme production. This is especially the case for "CO dehydrogenase" (CODH), the main biocatalyst that activates small molecules such as CO and CO2.

The distinctive feature of CODH is its active site consisting of a multi-metallic NiFe4S4 center, whose biosynthesis requires a specific multi-protein machinery that is still poorly understood.

In their previous work, researchers at Irig developed a CODH production system that uses the gene from a CO metabolizing bacterium (Rhodospirillum rubrum) expressed in the bacterium Escherichia coli. This process can produce an enzyme that is as stable and active as natural CODH, in a single purification step.

Now, the scientists are going even further by immobilizing the recombinant CODH on functionalized carbon nanotubes. They can thus create a stable bioelectro-catalytic system for several hours, which allows them to inter-convert CO2 into CO and vice versa. Current densities of 4.2 mA.cm-2 for CO2 reduction and 1.5 mA.cm-2 for CO oxidation have thereby been achieved.

The performance of this system compares favorably with electrochemical CO2 reduction processes using molecular catalysts. Furthermore, it has the added advantage of operating reversibly, under mild conditions and with very low overpotentials.

This work was supported by the Labex Arcane and was conducted in collaboration with researchers from Aix-Marseille University and Grenoble Alpes University.



Top page

Top page