Engineering cyanobacterial carbonic anhydrase surface mutations for fast CO2 hydration and capture
- 1Lawrence Berkeley National Laboratory
Abstract
Equilibration between CO 2 and the other forms of dissolved inorganic carbon (DIC) is slow under ambient conditions, bottlenecked by the hydration of dissolved CO 2 to form bicarbonate and a proton. This step is often rate-limiting for aqueous CO 2 capture processes under ambient temperature and pressure, and is precisely the chemistry catalyzed by the family of carbonic anhydrase enzymes. As a result, incorporation of carbonic anhydrases (CAs) into various CO 2 capture schemes may be used to accelerate CO 2 hydration, increasing the rates of downstream processes coupled to this DIC equilibrium. While this potential use for CA has been long-studied, extending these basic chemical principles to real applications have been hampered by practical questions of how to economically source carbonic anhydrase enzymes at mass scale. This work explores the use of modified cyanobacterial expression hosts as a potential resolution to that problem. Successful engineering of carbonic anhydrase surface display in fast-growing, marine cyanobacteria would yield a self-sustaining CO 2 hydration catalyst that requires only sunlight, CO 2 itself, and nutrients freely available in seawater, as inputs for passively generating carbonic anhydrases on the cell envelope during cell growth.
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BibTeX
@misc{agbo2026engineering,
title = {{Engineering cyanobacterial carbonic anhydrase surface mutations for fast CO2 hydration and capture}},
author = {Peter Agbo},
howpublished = {ChemRxiv},
year = {2026},
month = oct,
doi = {10.26434/chemrxiv-2025-0rnx8/v3},
url = {https://chemrxiv.org/doi/full/10.26434/chemrxiv-2025-0rnx8/v3},
note = {CC BY},
}
RIS
TY - UNPB
TI - Engineering cyanobacterial carbonic anhydrase surface mutations for fast CO2 hydration and capture
AU - Peter Agbo
PY - 2026
DA - 2026/10/22
PB - ChemRxiv
DO - 10.26434/chemrxiv-2025-0rnx8/v3
UR - https://chemrxiv.org/doi/full/10.26434/chemrxiv-2025-0rnx8/v3
AB - Equilibration between CO 2 and the other forms of dissolved inorganic carbon (DIC) is slow under ambient conditions, bottlenecked by the hydration of dissolved CO 2 to form bicarbonate and a proton. This step is often rate-limiting for aqueous CO 2 capture processes under ambient temperature and pressure, and is precisely the chemistry catalyzed by the family of carbonic anhydrase enzymes. As a result, incorporation of carbonic anhydrases (CAs) into various CO 2 capture schemes may be used to accelerate CO 2 hydration, increasing the rates of downstream processes coupled to this DIC equilibrium. While this potential use for CA has been long-studied, extending these basic chemical principles to real applications have been hampered by practical questions of how to economically source carbonic anhydrase enzymes at mass scale. This work explores the use of modified cyanobacterial expression hosts as a potential resolution to that problem. Successful engineering of carbonic anhydrase surface display in fast-growing, marine cyanobacteria would yield a self-sustaining CO 2 hydration catalyst that requires only sunlight, CO 2 itself, and nutrients freely available in seawater, as inputs for passively generating carbonic anhydrases on the cell envelope during cell growth.
ER -