AI summary

82% confidence

This study investigates Pseudomonas stutzeri S116, a sulfur-oxidizing bacterium isolated from marine sludge, as a bifunctional biocatalyst for both anodic and cathodic microbial fuel cells. Complete genome sequencing revealed 4,402 coding sequences with genes encoding cytochrome c, redox mediators (riboflavin and phenazine), type IV pili, and an integrated electron transport chain. The strain demonstrated maximum power densities of 765 mW/m² and 656.6 mW/m² in dual-chamber MFCs, with cyclic voltammetry confirming extracellular electron transfer capability. Metabolic pathways for thiosulfate oxidation and dissimilatory nitrate reduction suggest potential for wastewater treatment applications.

Generated by MESSAI extraction pipeline · review against source PDF

Generic MFCRepresentative model
Click to animate flow
loading 3D model…

Representative MFC — matched on the paper’s system type only, not its reactor or geometry.

Extraction

Reported parameters

4 extracted values

View extracted values

Open in lab for full controls, parameter editing, and template overlays.

Open in lab →

What they did

System
MFC

What worked

No outcome metrics extracted yet.

Abstract

Abstract Background Pseudomonas stutzeri S116 is a sulfur-oxidizing bacteria isolated from marine sludge. It exhibited excellent electricity generation as bioanode and biocathode applied in microbial fuel cells (MFCs). Complete genome sequencing of P. stutzeri and cyclic voltammetry method were performed to reveal its mechanism in microbial fuel cells system. Results This study indicated that the MFCs generated a maximum output voltage of 254.2 mV and 226.0 mV, and maximum power density of 765 mW/m 2 and 656.6 mW/m 2 respectively. Complete genome sequencing of P. stutzeri S116 was performed to indicate that most function genes showed high similarities with P. stutzeri , and its primary annotations were associated with energy production and conversion (6.84%), amino acid transport and metabolism (6.82%) and inorganic ion transport and metabolism (6.77%). Homology of 36 genes involved in oxidative phosphorylation was detected, which suggests the strain S116 possesses an integrated electron transport chain. Additionally, many genes encoding pilus-assembly proteins and redox mediators (riboflavin and phenazine) were detected in the databases. Thiosulfate oxidization and dissimilatory nitrate reduction were annotated in the sulfur metabolism pathway and nitrogen metabolism pathway, respectively. Gene function analysis and cyclic voltammetry indicated that P. stutzeri probably possesses cellular machinery such as cytochrome c and redox mediators and can perform extracellular electron transfer and produce electricity in MFCs. Conclusion The redox mediators secreted by P. stutzeri S116 were probably responsible for performance of MFCs. The critical genes and metabolic pathways involved in thiosulfate oxide and nitrate reduction were detected, which indicated that the strain can treat wastewater containing sulfide and nitrite efficiently.

Keywords

Pseudomonas stutzeriMicrobial fuel cellBiochemistrySulfur metabolismGeobacter sulfurreducensRedox

Identifiers

Journal
BMC Microbiology
Year
2022