Integrating PEGylated peptide-oriented bacteria-imprinted matrix and PdPt bimetallic-doped imidazolium zeolite framework-8 for sensitive detection of Escherichia coli with smartphone readout system

Abstract

Escherichia coli (E. coli) is one of the major foodborne pathogens, and its efficient isolation and detection from complex samples are crucial. Herein, we fabricated a novel hydrophilic-PEGylated peptide-oriented bacteria-imprinted PDMS matrix (HPBIM) for highly efficient capture of E. coli from complex samples. The antibody-free HPBIM possessed a hierarchical structure of imprinted cavities, which were inlaid with peptide-functionalized SiO2 (SiO2@peptide). Meanwhile, PEGylation was performed on the non-imprinted region of HPBIM to limit the non-specific absorption. So HPBIM could specifically capture target E. coli due to the synergistic effect of peptide affinity, bacteria-imprinting and PEGylation of non-imprinted region. Additionally, a new polyethylene glycol-covered / boronic acid-modified PdPt bimetallic-doped ZIF-8 (PBPPZ) was prepared for electively labeling E. coli captured by HPBIM. PBPPZ exhibited excellent peroxidase-like activity and could generate sensitive output signals, which could be further quantitatively determined by smartphone readout device. To prove the practicability, we proposed an innovative HPBIM-PBPPZ strategy, in which the HPBIM first selectively captured E. coli, then the PBPPZ specific labeled E. coli and oxidized colorless substrate into colored product, and finally the change in color was quantitatively determined by a smartphone readout device equipped with a Color Grab APP. The biomacromolecule-free HPBIM-PBPPZ strategy exhibited excellent sensitivity with limit of detection of 69 CFU mL−1 for grapefruit juice and 257 CFU mL−1 for milk, and was successfully applied in the determination of E. coli in spiked sample with recovery and relative standard deviation in the range of 88.1–106.7% and 4.0–7.8%, respectively. Therefore, we believe that the HPBIM-PBPPZ strategy has great potential to become a powerful tool for the ultrasensitive detection of pathogens in complex biological samples.