Related Experiment Video
Updated: Aug 15, 2026

Foodborne Pathogen Screening Using Magneto-fluorescent Nanosensor: Rapid Detection of E. Coli O157:H7
Published on: September 17, 2017
Mannose-engineered Eu-MOF for ratiometric fluorescent/colorimetric dual-detection and inhibition of E. coli
Weiqi Wu1, Zhen Wu1, Sihang Yuan1
1Institute for Frontier Medical Technology, College of Chemistry and Chemical Engineering, Shanghai University of Engineering Science, Shanghai, 201620, China.
Abstract:
Reliable detection and fast inhibition of Escherichia coli (E. coli) are critical for public health and food safety, so the detection-inhibition-integrated strategies become critical. Herein, a mannose-engineered 3,5-dicarboxyphenylboronic acid/curcumin dual-ligand Eu-metal-organic framework (Eu-MOF) was designed as dcMOF@man. Mannose realized the specific identification to E. coli; Eu-MOF exhibited dual-emission at 350 and 633 nm for robust ratiometric fluorescence sensing to E. coli as boronic acid-surface glycan interaction enhanced the emission at 350 nm, while mannose-FimH-mediated interaction attenuates the Eu3+ emission at 633 nm. The intensity ratio of I633/I350 exhibits a good linear relationship to E. coli at the concentration range of 10-107 CFU/mL with a low detection limit of 5 CFU/mL. Concurrently, the dcMOF@man exhibited peroxidase-like activity, enabling E. coli-dependent colorimetric detection based on tetramethylbenzidine oxidation, with the linear range of 10-107 CFU/mL and detection limit of 9 CFU/mL, which was also quantified via smartphone-based RGB analysis for on-site detection. The intrinsic antibacterial activity of curcumin afforded the effective inhibition of E. coli. Moreover, curcumin-mediated antibacterial activity synergizes with mannose targeting, resulting in nearly 100% antibacterial efficiency. Thus, dcMOF@man integrates targeting identification, ratiometric fluorescence sensing, colorimetric detection, and antibacterial functionality within single composite, as a generalizable strategy for on-site bacterial detection and inhibition.
