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基于抗菌肽介导的纳米复合物对的三明治免疫测定法,使用个人血糖仪作为读出物来测定大肠杆菌 O157:H7。

Sandwich immunoassay based on antimicrobial peptide-mediated nanocomposite pair for determination of Escherichia coli O157:H7 using personal glucose meter as readout.

机构信息

School of Chemical Engineering and Technology, Tianjin University, Tianjin, 300072, China.

Institute of Military Veterinary, Academy of Military Medical Sciences, Changchun, 130122, China.

出版信息

Mikrochim Acta. 2020 Mar 12;187(4):220. doi: 10.1007/s00604-020-4200-4.

Abstract

A sandwich immunoassay was developed for determination of E. coli O157:H7. This is based on an antimicrobial peptide-mediated nanocomposite pair and uses a personal glucose meter as signal readout. The antimicrobial peptides, magainins I, and cecropin P1 were employed as recognition molecules for the nanocomposite pair, respectively. With a one-step process, copper phosphate nanocomposites embedded by magainins I and FeO were used as "capturing" probes for bacterial magnetic isolation, and calcium phosphate nanocomplexes composed of cecropin P1 and invertase were used as signal tags. After magnetic separation, the invertase of the signal tags hydrolyzed sucrose to glucose, thereby converting E. coli O157:H7 levels to glucose levels. This latter can be quantified by a personal glucose meter. Under optimal conditions, the concentration of E. coli O157:H7 can be determined in a linear range of 10 to 10 CFU·mL with a detection limit of 10 CFU·mL. The method was successfully applied to the determination of E. coli O157:H7 in milk samples. Graphical abstract Schematic representation of sandwich immunoassay for E. coli O157:H7. One-pot synthetic of FeO-magainins I nanocomposites (MMP) were used for magnetic capture. Cecropin P1-invertase nanocomposites (PIP) were used as signal tags. A personal glucose meter was used as readout to determine the target.

摘要

夹心免疫测定法用于检测大肠杆菌 O157:H7。它基于抗菌肽介导的纳米复合材料对,并使用个人血糖仪作为信号读出。抗菌肽、magainins I 和 cecropin P1 分别用作纳米复合材料对的识别分子。采用一步法,嵌入 magainins I 和 FeO 的磷酸铜纳米复合材料被用作细菌磁性分离的“捕获”探针,而由 cecropin P1 和转化酶组成的磷酸钙纳米复合物则用作信号标签。在磁性分离后,信号标签的转化酶将蔗糖水解成葡萄糖,从而将大肠杆菌 O157:H7 的水平转换为葡萄糖水平。后者可以通过个人血糖仪进行定量。在最佳条件下,大肠杆菌 O157:H7 的浓度可以在 10 到 10 CFU·mL 的线性范围内确定,检测限为 10 CFU·mL。该方法成功应用于牛奶样品中大肠杆菌 O157:H7 的测定。

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