摘要
Escherichia coli ( E. coli ) is one of the most prevalent foodborne pathogens, releasing toxic substances and causing infectious and life-threatening diseases. Thus, the rapid and sensitive detection of E. coli is essential for safeguarding human health. Herein, a ratiometric colorimetric sensor was constructed for detecting E. coli , utilizing the coordination between zirconium (Zr)-tetraphenylporphyrin tetrasulfonic acid (TPPS) hydrate metal–organic frameworks (Zr-TMs) and copper ions (Cu 2+ ). E. coli can capture and convert external Cu 2+ into Cu + through its distinctive metabolic activities. This capability further enhances the coordination interaction between the porphyrin ligands in Zr-TMs and the metal ions. As a result, the ultraviolet–visible (UV–vis) absorption spectral properties of Zr-TMs changed, exhibiting an enhanced absorption peak at 413 nm (A 413 ) and a weakened peak at 434 nm (A 434 ). By monitoring the increase in ratio of A 413 to A 434 , this sensor achieved rapid and sensitive detection of E. coli at concentrations ranging from 10 2 to 10 7 CFU/mL within 63 min, with a detection limit of 19 CFU/mL. The color of the solution gradually changed from green to colorless. This proposed ratiometric method utilized the opposite changes in the two UV–vis absorption peak signals (A 413 and A 434 ) generated by the Zr-TMs probes, improving detection accuracy and achieving visual analysis. Additionally, this method accurately identified E. coli in milk samples, demonstrating substantial potential for detecting pathogenic bacteria in food.
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