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Abstract: Electrolyte pH tremendously affects the electricity output of microbial fuel cells. However, its underlying molecular mechanism remains elusive, in particular for Shewanella oneidensis MR-1, one of the most widely adopted electrogenic microorganisms. Herein, we found that MFCs were able to deliver a significant (but different) electricity output in a wide range of pH (from 6 to 10), with the maximum at pH=9 (alkaline), which delivers ∼1.5times’ higher power output than that at pH=7 (neutral). Furthermore, cyclic voltammetry analysis showed an enhanced electrochemical activity of riboflavin (responsible for extracellular electron transfer of Shewanella) at alkaline pH. Strikingly, the concentration of riboflavin synthesized by Shewanella in MFCs at different pH showed a good correlation with the electricity output of MFCs. Thus, our results substantiated that the increase of riboflavin biosynthesis by Shewanella at the alkaline condition underlies the improvement of the electricity output in MFCs. [Copyright &y& Elsevier]

Nitrogen doped carbon nanoparticles (NDCN) were applied to modify the carbon cloth anodes of microbial fuel cells (MFCs) inoculated with Shewanella oneidensis MR-1, one of the most well-studied exoelectrogens. Experimental results demonstrated that the use of NDCN increased anodic absorption of flavins ( i.e. , the soluble electron mediator secreted by S. oneidensis MR-1), facilitating shuttle-mediated extracellular electron transfer. In addition, we also found that NDCN enabled enhanced contact-based direct electron transfer via outer-membrane c-type cytochromes. Taken together, the performance of MFCs with the NDCN-modified anode was enormously enhanced, delivering a maximum power density 3.5 times’ higher than that of the MFCs without the modification of carbon cloth anodes. [ABSTRACT FROM AUTHOR]

[Display omitted] • Shewanella loihica PV-4 exhibited high performance in reducing CO 2 to formate. • A novel three-dimensional biological self-assembled cathode was constructed. • No involvement of electron mediators was found in whole cell catalysis. • Faraday efficiency of bioelectrosynthetic CO 2 -to-formate reached 99.95%. Bioelectrochemical CO 2 reduction (bio-CO 2 R) provides a sustainable and carbon neutral power-to-chemical route. Whole-cell electrosynthesis is one of the attractive strategies to realize CO 2 R due to its simple and low-cost superiorities. However, it is still challenging to overcome the sluggish transmembrane electron transfer of microorganisms without exogenously added mediators. Here, we described the fabrication of biohydrogel that contains bio-reduced graphene oxide (rGO) and living electroactive bacteria (EAB) for bio-CO 2 R. The EAB exhibited surprising ability to self-assemble biohydrogel that was further served as biocathode to drive CO 2 -to-formate electrosynthesis. With the close interaction between EAB and rGO nanosheets, the transmembrane electron transfer achieved at high Faradaic efficiency (∼99.5 %) and 46-fold increase of formate titer without exogenous mediator. This work provided the facile and practical approach to bridge the bacterial cell and electrode for efficient electron transfer and implied the new possibility to store the electric energy into chemicals with bio-CO 2 R. [ABSTRACT FROM AUTHOR]

Although microbial fuel cells (MFCs) is considered as one of the most promising technology for renewable energy harvesting, low power output still accounts one of the bottlenecks and limits its further development. In this work, it is found that Cu 2+ (0.1 μg L −1 –0.1 mg L −1 ) or Cd 2+ (0.1 μg L −1 –1 mg L −1 ) significantly improve the electricity generation in MFCs. The maximum power output achieved with trace level of Cu 2+ (∼6 nM) or Cd 2+ (∼5 nM) is 1.3 times and 1.6 times higher than that of the control, respectively. Further analysis verifies that addition of Cu 2+ or Cd 2+ effectively improves riboflavin production and bacteria attachment on the electrode, which enhances bacterial extracellular electron transfer (EET) in MFCs. These results unveil the mechanism for power output enhancement by Cu 2+ or Cd 2+ addition, and suggest that metal ion addition should be a promising strategy to enhance EET as well as power generation of MFCs. [ABSTRACT FROM AUTHOR]

• Cytocompatible bacterial ATRP (b- ATRP) was developed. • Bacterial nanohybrids with high viability were obtained with b -ATRP. • The surface electric property of bacterial cells was well-controlled by b- ATRP. • Cr(VI) removal rate was improved by 3 times with bacterial nanohybrid. Surface-initiated activator regenerated by electron transfer atom transfer radical polymerization (SI-ARGET ATRP) has great potential to modify living cell surface with controlled architecture and tailored phenotype. However, it is challenging to engineer the bacterial cells with current SI-ARGET ATRP due to low cellular tolerance to the toxic reagents in polymerization. In this study, a cytocompatible bacterial SI-ARGET ATRP (b -ATRP) strategy was developed for individual nanoencapsulation of living bacterial cell. With step by step optimization of reaction conditions, living nanohybrid with high cell viability (>70%) was achieved with b -ATRP. Furthermore, living Shewanella nanohybrids with controllable surface electric property were fabricated with b -ATRP and applied for aqueous Cr(VI) treatment. Impressively, nanoencapsulation of cells with poly(4-vinylpyridine) improved the Cr(VI) removal rate by 3 times. This work provided a new approach to engineer the living bacterial cell surface and expanded the ATRP applications to prokaryotic cell and bioremediation. [ABSTRACT FROM AUTHOR]