Enhanced Microbial Protein Production from CO 2 and Air by a MoS 2 Catalyzed Bioelectrochemical System.
Lixia ZhangLizhen ZengJingting WangHaoran WangDecong ZhengXiaomei WangDaping LiGuoqiang ZhanPublished in: ChemPlusChem (2024)
Carbon dioxide can be relatively easily reduced to organic matter in a bioelectrochemical system (BES). However, due to insufficient reduction force from in-situ hydrogen evolution, it is difficult for nitrogen reduction. In this study, MoS 2 was firstly used as an electrocatalyst for the simultaneous reduction of CO 2 and N 2 to produce microbial protein (MP) in a BES. Cell dry weight (CDW) could reach 0.81±0.04 g/L after 14 d operation at -0.7 V (vs. RHE), which was 108±3 % higher than that from non-catalyst control group (0.39±0.01 g/L). The produced protein had a better amino acid profile in the BES than that in a direct hydrogen system (DHS), particularly for proline (Pro). Besides, MoS 2 promoted the growth of bacterial cell on an electrode and improved the biofilm extracellular electron transfer (EET) by microscopic observation and electrochemical characterization of MoS 2 biocathode. The composition of the microbial community and the relative abundance of functional enzymes revealed that MoS 2 as an electrocatalyst was beneficial for enriching Xanthobacter and enhancing CO 2 and N 2 reduction by electrical energy. These results demonstrated that an efficient strategy to improve MP production of BES is to use MoS 2 as an electrocatalyst to shift amino acid profile and microbial community.
Keyphrases
- microbial community
- room temperature
- amino acid
- quantum dots
- antibiotic resistance genes
- reduced graphene oxide
- visible light
- carbon dioxide
- single cell
- highly efficient
- ionic liquid
- transition metal
- electron transfer
- gold nanoparticles
- organic matter
- cell therapy
- protein protein
- binding protein
- staphylococcus aureus
- pseudomonas aeruginosa
- small molecule
- weight loss
- escherichia coli
- single molecule
- weight gain