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Updated: Jan 10, 2026

Waste Water Derived Electroactive Microbial Biofilms: Growth, Maintenance, and Basic Characterization
Published on: December 29, 2013
Interfacing nitrogen biochemistry with electrochemical output in Saccharomyces cerevisiae microbial fuel cells
Marcelinus Christwardana1, Muhammad Fahrul Riza2, Purbowatiningrum Ria Sarjono2
1Department of Chemistry, Faculty of Science and Mathematics, Diponegoro University, Semarang 50275, Indonesia; Master Program of Energy, School of Postgraduate Studies, Diponegoro University, Semarang 50241, Indonesia; Research Collaboration Center for Electrochemistry, BRIN - Diponegoro University, Semarang 50275, Indonesia.
Abstract:
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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