Find in Library

The need for greener processes to satisfy the demand of platform chemicals together with the possibility of reusing CO₂ from human activities has recently encouraged research on the set-up, optimization, and development of bioelectrochemical systems (BESs) for the electrosynthesis of organic compounds from inorganic carbon (CO₂, HCO₃⁻). In the present study, we tested the ability of <i>Clostridium saccharoperbutylacetonicum</i> N1-4 (DSMZ 14923) to produce acetate and D-3-hydroxybutyrate from inorganic carbon present in a CO₂:N₂ gas mix. At the same time, we tested the ability of a <i>Shewanella oneidensis</i> MR1 and <i>Pseudomonas aeruginosa</i> PA1430/CO1 consortium to provide reducing power to sustain carbon assimilation at the cathode. We tested the performance of three different systems with the same layouts, inocula, and media, but with the application of 1.5 V external voltage, of a 1000 Ω external load, and without any connection between the electrodes or external devices (open circuit voltage, OCV). We compared both CO₂ assimilation rate and production of metabolites (formate, acetate 3-D-hydroxybutyrate) in our BESs with the values obtained in non-electrogenic control cultures and estimated the energy used by our BESs to assimilate 1 mol of CO₂. Our results showed that <i>C. saccharoperbutylacetonicum</i> NT-1 achieved the maximum CO₂ assimilation (95.5%) when the microbial fuel cells (MFCs) were connected to the 1000 Ω external resistor, with the <i>Shewanella</i>/<i>Pseudomonas</i> consortium as the only source of electrons. Furthermore, we detected a shift in the metabolism of <i>C. saccharoperbutylacetonicum</i> NT-1 because of its prolonged activity in BESs. Our results open new perspectives for the utilization of BESs in carbon capture and electrosynthesis of platform chemicals.