Primary technical activities focused on testing GDEs for effective CO2 capture, selecting appropriate biocatalysts for both the bioanode and biocathode, and developing a prototype MES system. To achieve this, a number of gas-diffusion bioelectrodes (GDBs) was tested, promoting stable biofilm growth and bio-electrochemical CO2 conversion. The project team also optimized a bioanode specifically for glycerol oxidation, enhancing the MES’s overall functionality. Bioelectrochemical tests, including cyclic voltammetry and chronoamperometry, revealed increased current densities and intensified redox peaks, suggesting heightened electrocatalytic activity with CO2-based MES. High-performance liquid chromatography (HPLC) confirmed increased production of volatile fatty acids (VFAs), particularly of acetate, propionate, and butyrate, demonstrating improved CO2 conversion into valuable chemicals. The key outcome was the improvement in current density and stability of MES systems fed with CO2 compared to those using bicarbonate, indicating enhanced system efficiency. Microbial enrichment and community analyses were conducted to better understand biofilm dynamics. The integrated dual bio-catalytic MES system has successfully merged CO2 reduction with glycerol oxidation, establishing a foundational technology for efficient CO2 transformation. The integrated bio-catalytic MES system was implemented, achieving a combination of CO2-reducing and glycerol-oxidizing functionalities.