Work

Accelerated carbonate weathering by immobilized recombinant carbonic anhydrase

Year: 2025

Type: article

Abstract: CO 2 absorption in aqueous alkaline solutions promoted by carbonic anhydrase (CA) has received increased attention as a solution for post-combustion CO 2 capture. In particular, accelerated weathering has emerged as an alternative approach for CO 2 capture, mimicking nature’s way to sequestrate CO 2 . In this study, an evolved CA from Desulfovibrio vulgaris was immobilized on magnetic nanoparticles (MNPs) offering a promising solution for the effective enzyme separation and recovery from complex and heterogeneous reaction media. The immobilization yields were high (86–98 %) and MNPs-D v CA8.0 were characterized based on standardized CO 2 release and CO 2 absorption assays and compared to the free enzyme. As a following step, MNPs-D v CA8.0 were applied as promoter in the accelerated weathering of insoluble lime mud, originating as a residue from a paper and pulp industry. MNPs-D v CA8.0 could be efficiently separated, washed and reused for up to 10 consecutive reaction cycles, offering a biocatalyst productivity equal to 2.83 g captured CO 2 /g CA opposite to the free enzyme that offered only 1.01 g captured CO 2 /g CA. CA immobilization could offer a mitigation strategy for the non-selective adsorption of the free enzyme on lime mud particles during the CO 2 capturing reaction. The highly reproducible and robust immobilization method, that provides material separation based on its magnetic properties, could be a viable solution for the recovery of enzyme and its separation from the lime mud slurry, aiding in obtaining a highly pure solution rich in bicarbonate, as product. • D v CA8.0 from Desulfovibrio vulgaris was immobilized on magnetic nanoparticles (MNPs). • MNPs D v CA8.0 were characterized based on standard assays and compared with the free enzyme. • MNPs D v CA8.0 were applied in the accelerated weathering offering > 2.5-times higher biocatalyst productivity. • MNPs D v CA8.0 would be reused for up to 10 consecutive cycles.

Source: Journal of CO2 Utilization

DOI: 10.1016/j.jcou.2025.103050