UV-induced oxidase activity of carbon dots in visible UVA dosage, Escherichia coli quantification and bacterial typing

Anal Chim Acta. 2024 Feb 1:1288:342140. doi: 10.1016/j.aca.2023.342140. Epub 2023 Dec 17.

Abstract

Ultraviolet (UV) light and foodborne pathogenic bacteriais are an important risk to the environment's safety. They endanger human health, and also lead to outbreaks of infectious disease, posing great threats to global public health security, national economy, and social stability. The appearance of carbon dot (CD) nanozymes offers a new perspective to solve the problems of detection of UV light and pathogenic bacteria in environment. This paper reports the preparation of CDs with dual enzyme-like activities (superoxide dismutase activity and UV-induced oxidase activity). The product can catalyze the oxidation of the substrate 3, 3', 5, 5'-tetramethylbenzidine (TMB) under UV light (365 nm) to achieve rapid color development. Based on the excellent fluorescence properties of CDs, the colorimetric-fluorescence dual-channel real-time detection of UVA dose was realized, the mechanism underlying the catalytic oxidation of TMB by UV-induced oxidase CDs was also investigated. Furthermore, a portable CDs-TMB-PA hydrogel was prepared which could realize the real-time monitoring of UV in outdoor environment with the assistance of smartphone. Based on the pH dependency of the CD nanozymes and specific glycolytic response of the pathogenic bacteria Escherichia coli (E. coli) O157:H7, the direct, simple, quick, and sensitive typing and detection have been realized. This research offers new perspectives for studying CD nanozymes and their applications in UV and bacterial detection, demonstrating the remarkable potential of CD nanozymes in detecting environmental hazards.

Keywords: Carbon dot nanozymes; Escherichia coli O157:H7; Photocatalysis; Portable gel; Ultraviolet A dose; Visual detection.

MeSH terms

  • Bacteria
  • Bacterial Typing Techniques
  • Carbon
  • Catalysis
  • Escherichia coli O157*
  • Humans
  • Oxidoreductases*

Substances

  • Oxidoreductases
  • Carbon