Transcription factor-based whole-cell
biosensors have recently
become promising alternatives to conventional analytical methods due
to their advantage of simplicity, cost-effectiveness, and environmental
friendliness. In this study, we used genetic engineering to develop
a whole-cell biosensor based on the activation of promoters by CupR
via interactions with gold ions, leading to the expression of reporter
genes that yield output signals. Altering the promoter sequences was
shown to significantly improve the performance of the biosensor strain
in terms of gold-specificity. The detection sensitivity of our engineered
strains was 42-fold higher than that of wild-type strains. The linear
range of the purposed sensor was 125–1000 nM with a limit of
detection at 46.5 nM. The effectiveness of the sensor strain was verified
in wastewater samples.