Microbial fuel cells (MFCs) utilize microbial metabolism to convert organic substrates into electrical energy. Saccharomyces cerevisiae presents a promising eukaryotic biocatalyst due to its fermentative capacity and non-pathogenic nature, yet its electron transfer efficiency remains a major bottleneck. This study evaluates the influence of nitrogen source variation, peptone, tryptone, and bovine serum albumin (BSA) at concentrations of 1, 2.5, and 5 mg.mL-1 on the electrochemical performance of Saccharomyces cerevisiae-based MFCs. Half-cell analyses, including cyclic voltammetry and rate-determining step (RDS) assessments, revealed diffusion-controlled electron transfer via cytochromes. The highest electron transfer rate constant (Ks) was obtained with peptone 5 mg.mL-1 (1.61 ± 0.285 s-1), followed by tryptone 1 mg.mL-1 (1.53 ± 0.332 s-1) and BSA 1 mg.mL-1 (0.95 ± 0.055 s-1). Full-cell experiments showed maximum voltage outputs of 0.132 V (peptone 5 mg.mL-1), 0.117 V (tryptone 1 mg.mL-1), and 0.039 V (BSA 1 mg.mL-1), and corresponding peak power densities of 46.6, 44.0, and 7.1 mW m-2. SEM confirmed enhanced biofilm formation with increased nitrogen concentration, supporting stronger electrochemical activity. These results highlight nitrogen source optimization as a strategic approach to enhance microbial electron transfer and energy yield in yeast-based MFC systems.
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| Evidence ID | Analyze ID | Gene/Complex | Systematic Name/Complex Accession | Qualifier | Gene Ontology Term ID | Gene Ontology Term | Aspect | Annotation Extension | Evidence | Method | Source | Assigned On | Reference |
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| Evidence ID | Analyze ID | Gene | Gene Systematic Name | Phenotype | Experiment Type | Experiment Type Category | Mutant Information | Strain Background | Chemical | Details | Reference |
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| Evidence ID | Analyze ID | Gene | Gene Systematic Name | Disease Ontology Term | Disease Ontology Term ID | Qualifier | Evidence | Method | Source | Assigned On | Reference |
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| Evidence ID | Analyze ID | Regulator | Regulator Systematic Name | Target | Target Systematic Name | Direction | Regulation of | Happens During | Regulator Type | Direction | Regulation Of | Happens During | Method | Evidence | Strain Background | Reference |
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| Site | Modification | Modifier | Source | Reference |
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| Evidence ID | Analyze ID | Interactor | Interactor Systematic Name | Interactor | Interactor Systematic Name | Allele | Assay | Annotation | Action | Phenotype | SGA score | P-value | Source | Reference | Note |
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| Evidence ID | Analyze ID | Interactor | Interactor Systematic Name | Interactor | Interactor Systematic Name | Assay | Annotation | Action | Modification | Source | Reference | Note |
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| Complement ID | Locus ID | Gene | Species | Gene ID | Strain background | Direction | Details | Source | Reference |
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| Evidence ID | Analyze ID | Dataset | Description | Keywords | Number of Conditions | Reference |
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