Increasing industrialization and urbanization have contributed to a significant rise in wastewater discharge and exerted extensive pressure on the existing natural energy resources. Microbial fuel cell (MFC) is a sustainable technology that utilizes wastewater for electricity generation. MFC comprises a bioelectrochemical system employing electroactive biofilms of several aerobic and anaerobic bacteria, such as Geobacter sulfurreducens, Shewanella oneidensis, Pseudomonas aeruginosa, and Ochrobacterum pseudiintermedium. Since the electroactive biofilms constitute a vital part of the MFC, it is crucial to understand the biofilm-mediated pollutant metabolism and electron transfer mechanisms. Engineering electroactive biofilm communities for improved biofilm formation and extracellular polymeric substances (EPS) secretion can positively impact the bioelectrochemical system and improve fuel cell performance. This review article summarizes the role of electroactive bacterial communities in MFC for wastewater treatment and bioelectricity generation. A significant focus has been laid on understanding the composition, structure, and function of electroactive biofilms in MFC. Various electron transport mechanisms, including direct electron transfer (DET), indirect electron transfer (IET), and long-distance electron transfer (LDET), have been discussed. A detailed summary of the optimization of process parameters and genetic engineering strategies for improving the performance of MFC has been provided. Lastly, the applications of MFC for wastewater treatment, bioelectricity generation, and biosensor development have been reviewed.
Keyphrases
- electron transfer
- wastewater treatment
- biofilm formation
- pseudomonas aeruginosa
- candida albicans
- staphylococcus aureus
- antibiotic resistance genes
- cystic fibrosis
- single cell
- acinetobacter baumannii
- escherichia coli
- cell therapy
- drug delivery
- induced apoptosis
- mesenchymal stem cells
- gene expression
- cancer therapy
- gold nanoparticles
- bone marrow
- high intensity
- dna methylation
- drug resistant
- cell proliferation
- multidrug resistant
- cell cycle arrest
- combination therapy
- pi k akt
- replacement therapy
- label free
- smoking cessation
- cell death