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Graphene composite has been widely used in various bioelectrochemical systems (BES). However, it is suffered from tedious fabrication procedure and ambiguous mechanism for its effect on BES. Here, a one-step and in-situ strategy for simultaneously graphene exfoliation and aniline polymerization was developed for fabrication of graphene/PANI composite electrode (GO/PANI OS ). This GO/PANI OS outperformed graphite paper (GP), GP with PANI (GP/PANI) and GP with electrochemical exfoliated graphene (GO H2SO4 ) in Shewanella oneidensis MR-1 inoculated BES (improved the power density output, i.e., 24, 3.4 and 5.7 times of GP , GP/PANI and GO H2SO4 , respectively). Further analysis revealed a synergistic improvement on both direct and mediated extracellular electron transfer of S. oneidensis MR-1 by GO/PANI OS contributed to its performance enhancement in BES. This work not only provided a simple strategy for graphene composite fabrication, but also unveiled the underlying mechanism for its stimulation on BES, which promises new opportunity of graphene composite application in various biosystems., (Copyright © 2016 Elsevier B.V. All rights reserved.)

Fumarate is of great importance as it is an oncometabolite as well as food spoilage indicator. However, cost-effective and fast quantification method for fumarate is lacking although it is urgently required. This work developed an electrochemical whole-cell biosensing system for fumarate quantification. A sensitive inwards electric output (electron flow from electrode into bacteria) responded to fumarate in Shewanella oneidensis MR-1 was characterized, and an electrochemical fumarate biosensing system was developed without genetic engineering. The biosensing system delivered symmetric current peak immediately upon fumarate addition, where the peak area increased in proportion to the increasing fumarate concentration with a wide range of 2 μM-10 mM (R(2)=0.9997). The limit of detection (LOD) and the limit of quantification (LOQ) are 0.83 μM and 1.2 μM, respectively. This biosensing system displayed remarkable specificity to fumarate against other possible interferences. It was also successfully applied to samples of apple juice and kidney tissue. This study added new dimension to electrochemical biosensor design, and provide a simple, cost-effective, fast and robust tool for fumarate quantification., (Copyright © 2014 Elsevier B.V. All rights reserved.)

Toxicity assessment of water is of great important to the safety of human health and to social security because of more and more toxic compounds that are spilled into the aquatic environment. Therefore, the development of fast and reliable toxicity assessment methods is of great interest and attracts much attention. In this study, by using the electrochemical activity of Shewanella oneidensis MR-1 cells as the toxicity indicator, 3,5-dichlorophenol (DCP) as the model toxic compound, a new biosensor for water toxicity assessment was developed. Strikingly, the presence of DCP in the water significantly inhibited the maximum current output of the S. oneidensis MR-1 in a three-electrode system and also retarded the current evolution by the cells. Under the optimized conditions, the maximum current output of the biosensor was proportional to the concentration of DCP up to 30 mg/L. The half maximal inhibitory concentration of DCP determined by this biosensor is about 14.5 mg/L. Furthermore, simultaneous monitoring of the retarded time (Δ t) for current generation allowed the identification of another biosensor signal in response to DCP which could be employed to verify the electrochemical result by dual confirmation. Thus, the present study has provided a reliable and promising approach for water quality assessment and risk warning of water toxicity. [ABSTRACT FROM AUTHOR]

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]

• 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]

• Size-controlled biosynthesis of FeS nanoparticles was achieved. • Cr(VI) removal capacity of 565.6 mg/g was achieved by FeS NP with size of 30–40 nm. • Small nanoparticle size reduced FeS passivation in Cr(VI) treatment. In this study, biogenic iron sulfide nanoparticles (FeS NPs) were synthesized by Shewanella and used for Cr(VI) removal. To control the size of FeS NPs, the biological S(-II) releasing rate was proposed as the key parameter in Fe(III) reduction and was subtly tuned with the aid of a kinetic model. Field emission scanning electron microscope (FESEM) observation revealed that gradually increased S(-II) releasing rate lead to the formation of FeS NPs with size from 30 nm to 90 nm. Impressively, the biogenic FeS NPs with 30–40 nm showed high removal rate and large removal capacity (565.6 mg/g) for removal of aqueous Cr(VI). Further analyses revealed that the improved performance of small FeS NPs was ascribed to the reduced passivation of FeS. Therefore, this study provided a facile approach for size-controlled biosynthesis of FeS NPs, and demonstrated the promise to use biogenic FeS NPs for chromate remediation. [ABSTRACT FROM AUTHOR]