Abstract
The healthcare industry emits significant amounts of CO2and has an imperative need for decarbonization. This study demonstrated a new hybrid electro-enzymatic process that converts waste CO2into high-value C6 pharmaceutical precursor compounds. A novel three-chamber electrolyzer equipped with a Cu-based gas diffusion electrode converted gaseous CO2into ethanol at a high current density (40-60 mA/cm2), high selectivity (43-81 mol %), and production rate (368-428 mg/L/h). Purified ethanol from the electrolyzer was then sent to an enzymatic bioreactor where ADH and DERA enzymes upgraded ethanol into C6 statin precursor molecules at high yields (29-35%) via acetaldehyde. Competitive C6 lactol synthesis rates (4.7-5.7 mM/day) and titers (712-752 mg/L) were achieved, demonstrating the potential of the end-to-end process. The C6 lactol product can seamlessly be converted to statins, a class of lipid-lowering medication that is among the largest selling class of drugs in the world. This hybrid process provides a new pathway for CO2valorization to high-value products and accelerates healthcare sector decarbonization.
Original language | English (US) |
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Pages (from-to) | 4114-4121 |
Number of pages | 8 |
Journal | ACS Sustainable Chemistry and Engineering |
Volume | 10 |
Issue number | 13 |
DOIs | |
State | Published - Apr 4 2022 |
Externally published | Yes |
All Science Journal Classification (ASJC) codes
- General Chemistry
- Environmental Chemistry
- General Chemical Engineering
- Renewable Energy, Sustainability and the Environment
Keywords
- 2-deoxy-ribose-5-phosphate aldolase
- COvalorization
- electro-enzymatic synthesis
- hybrid COreduction
- sustainable chemicals