{"title":"A nano-biosensing platform based on CuS-BSA for label-free fluorescence detection of Escherichia coli†","authors":"Xiaoqing Zhang, Shanglin Li and Mei Liu","doi":"10.1039/D4AN01060D","DOIUrl":null,"url":null,"abstract":"<p >Bacterial contamination is a serious issue for public health and food safety. In this work, a simple and label-free fluorescence detection nanoplatform for <em>Escherichia coli</em> (<em>E. coli</em>) was established on the basis of the competitive relationship for the reduction of Cu<small><sup>2+</sup></small> in CuS-BSA between <em>E. coli</em> and <em>O</em>-phenylenediamine (OPD). OPD could be directly oxidized by Cu<small><sup>2+</sup></small> to produce 2,3-diaminophenazine (ox OPD) with fluorescence properties. When OPD was introduced into an aqueous solution containing CuS-BSA and <em>E. coli</em>, the oxidation of OPD was inhibited owing to the reduction of Cu<small><sup>2+</sup></small> to Cu<small><sup>+</sup></small>/Cu<small><sup>0</sup></small> by NADH-2 dehydrogenase in the bacterial copper homeostasis mechanism, thus decreasing the fluorescence response signal of the system. Meanwhile, our strategy exhibited a satisfactory performance with a broad linear response to <em>E. coli</em> ranging from 12 to 1.2 × 10<small><sup>7</sup></small> CFU mL<small><sup>−1</sup></small>, and the limit of detection was 9 CFU mL<small><sup>−1</sup></small>. The practicability of the developed fluorescence biosensing platform in real samples was evaluated by successful determination of <em>E. coli</em> in drinking water and orange juice. These findings provide a new sensing strategy for analyzing other foodborne bacteria and ensuring food safety assessment.</p>","PeriodicalId":63,"journal":{"name":"Analyst","volume":" 22","pages":" 5394-5400"},"PeriodicalIF":3.6000,"publicationDate":"2024-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Analyst","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/an/d4an01060d","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Bacterial contamination is a serious issue for public health and food safety. In this work, a simple and label-free fluorescence detection nanoplatform for Escherichia coli (E. coli) was established on the basis of the competitive relationship for the reduction of Cu2+ in CuS-BSA between E. coli and O-phenylenediamine (OPD). OPD could be directly oxidized by Cu2+ to produce 2,3-diaminophenazine (ox OPD) with fluorescence properties. When OPD was introduced into an aqueous solution containing CuS-BSA and E. coli, the oxidation of OPD was inhibited owing to the reduction of Cu2+ to Cu+/Cu0 by NADH-2 dehydrogenase in the bacterial copper homeostasis mechanism, thus decreasing the fluorescence response signal of the system. Meanwhile, our strategy exhibited a satisfactory performance with a broad linear response to E. coli ranging from 12 to 1.2 × 107 CFU mL−1, and the limit of detection was 9 CFU mL−1. The practicability of the developed fluorescence biosensing platform in real samples was evaluated by successful determination of E. coli in drinking water and orange juice. These findings provide a new sensing strategy for analyzing other foodborne bacteria and ensuring food safety assessment.