A better understanding of the biological functions of microorganism is required to reduce their threats and increase their usefulness. Therefore, an importance of real-time evaluation of bacterial activity increase for various purposes such as hygiene management, development of antibacterial agents, and effective utilization of bacterial resources.1 This necessitates a quantitative assessment of metabolic processes, including growth and respiration. Here we would like to introduce the development of electrochemical methods for assessing bacterial activity.Electrochemical detection of viable bacterial cells was performed using cell membrane permeable electron mediator and redox active pigment. Shewanella oneidensis MR-1 transfers electrons generated within the cell to the extracellular environment via the cytochrome complex in the inner/outer membranes and is one of the most useful bacteria for the recovery of metals, treatment of wastewater, and preparation of microbial fuel cells. By using potentiometric measurements, we have examined intracellular electron generation in bacterial suspensions of S. oneidensis supplemented with different carbon sources or ferricyanide, which was almost completely reduced to ferrocyanide during the incubation without affecting bacterial cell viability.2 On the other hand, a tetrazolium salt (MTT), which was converted to an insoluble reduction form (formazan) through the respiration of microbial cells.3 The insolubility of this formazan was effectively exploited as a surface-confined redox event. The electrochemical detection of formazan was effectively coupled with the thermal lysis of microbes. The sensitivity of the present technique is up to 10,000-fold higher than that of MTT colorimetry and requires an incubation time of only 1 h, which is approximately 1/4 of that required for other metabolism-based techniques. Furthermore, the measurement of the reduction current of dissolved oxygen provides an effective mean for assessing the respiratory activity of bacteria in suspension.4 1) T. Kinoshita, K. Ishiki, D. Q. Nguyen, H. Shiigi, T. Nagaoka, Anal. Chem., 90(6), 4098 (2018).2) K. Ishiki, H. Shiigi, Anal. Chem., 91(22), 14401-14406 (2019).3) K. Ishiki, D. Q. Nguyen, A. Morishita, H. Shiigi, T. Nagaoka, Anal. Chem., 90(18), 10903 (2018).4) M. Saito, K. Ishiki, D. Q. Nguyen, H. Shiigi, Anal. Chem., 91(20), 12793-12798 (2019).