Multichannel bioelectronic sensing using engineered Escherichia coli.

Zhang, Xu; Charrier, Marimikel; Ajo-Franklin, Caroline M · Nat Commun · 2025

basic_science · Level V

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Abstract

To advance environmental health and hazard detection, researchers have developed whole-cell bioelectronic sensors by engineering extracellular electron transfer to be dependent on an analyte<sup>1</sup>. However, these sensors regulate a single electron transfer pathway as an electrochemical channel, limiting the sensing information to a single analyte. We have developed a multichannel bioelectronic sensor where different chemicals regulate distinct extracellular electron transfer pathways within a single Escherichia coli cell. One channel utilizes the flavin synthesis pathway from Bacillus subtilis<sup>2</sup> and is controlled by a cadmium-responsive promoter. Another channel, the CymA-Mtr pathway from Shewanella oneidensis<sup>3</sup>, is controlled by an arsenite-responsive promoter and activates cytochrome CymA expression<sup>4,5</sup>. We exploit the differing redox potentials of the two extracellular electron transfer pathways<sup>6</sup> to develop a redox-potential-dependent algorithm that efficiently converts biological signals into 2-bit binary outputs. This enables our bioelectronic sensor to detect and differentiate heavy metals at EPA limits. When deployed in complex environmental water samples, our sensor effectively and accurately encodes 2-bit binary signals across various analyte conditions. Thus, our multichannel bioelectronic sensor advances the field through simultaneous detection of different chemicals by a single cell, significantly expanding information transmission and helping to safeguard human and environmental health.

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