Journal
ANALYTICAL CHEMISTRY
Volume 94, Issue 20, Pages 7210-7218Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.2c00055
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Funding
- National Natural Science Foundation of China [22134003]
- UK Research and Innovation Future Leaders Fellowship [MR/S018875/1]
- US Office of Naval Research Global grant [N62909-20-1-2036]
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This study improves the performance of whole-cell biosensors for arsenic contamination by optimizing the promoter design. The arsenic-responsive system from Escherichia coli is used as the sensing element, and a genetic circuit is constructed to characterize the refactored promoters. A novel promoter with maximal repression efficiency and optimal fold change is discovered, and high sensitivity fluorescence and colorimetric sensors are developed for quantifying arsenic levels in groundwater.
Whole-cell biosensors for arsenic contamination are typically designed based on natural bacterial sensing systems, which are often limited by their poor performance for precisely tuning the genetic response to environmental stimuli. Promoter design remains one of the most important approaches to address such issues. Here, we use the arsenic-responsive ArsR-P-ars regulation system from Escherichia coli MG1655 as the sensing element and coupled gfp or lacZ as the reporter gene to construct the genetic circuit for characterizing the refactored promoters. We first analyzed the ArsR binding site and a library of RNA polymerase binding sites to mine potential promoter sequences. A set of tightly regulated P-ars promoters by ArsR was designed by placing the ArsR binding sites into the promoter's core region, and a novel promoter with maximal repression efficiency and optimal fold change was obtained. The fluorescence sensor P-lacV-P-arsOC2 constructed with the optimized P-arsOC2 promoter showed a fold change of up to 63.80-fold (with green fluorescence visible to the naked eye) at 9.38 ppb arsenic, and the limit of detection was as low as 0.24 ppb. Further, the optimized colorimetric sensor P-lacV-P-arsOC2-lacZ with a linear response between 0 and 5 ppb was used to perform colorimetric reactions in 24-well plates combined with a smartphone application for the quantification of the arsenic level in groundwater. This study offers a new approach to improve the performance of bacterial sensing promoters and will facilitate the on-site application of arsenic whole-cell biosensors.
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