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开发一种生物传感器蛋白子弹作为快速检测饮用水中大肠杆菌的荧光方法。

Development of a biosensor protein bullet as a fluorescent method for fast detection of Escherichia coli in drinking water.

作者信息

Gutiérrez-Del-Río Ignacio, Marín Laura, Fernández Javier, Álvarez San Millán María, Ferrero Francisco Javier, Valledor Marta, Campo Juan Carlos, Cobián Natalia, Méndez Ignacio, Lombó Felipe

机构信息

Research Group BIONUC, Departamento de Biología Funcional, Área de Microbiología, University of Oviedo, Oviedo, Principality of Asturias, Spain.

Department of Electric, Electronic, Computer and Systems Engineering, University of Oviedo, Campus of Gijón, Gijón, Principality of Asturias, Spain.

出版信息

PLoS One. 2018 Jan 5;13(1):e0184277. doi: 10.1371/journal.pone.0184277. eCollection 2018.

Abstract

Drinking water can be exposed to different biological contaminants from the source, through the pipelines, until reaching the final consumer or industry. Some of these are pathogenic bacteria and viruses which may cause important gastrointestinal or systemic diseases. The microbiological quality of drinking water relies mainly in monitoring three indicator bacteria of faecal origin, Escherichia coli, Enterococcus faecalis and Clostridium perfringens, which serve as early sentinels of potential health hazards for the population. Here we describe the analysis of three chimeric fluorescent protein bullets as biosensor candidates for fast detection of E. coli in drinking water. Two of the chimeric proteins (based on GFP-hadrurin and GFP-pb5 chimera proteins) failed with respect to specificity and/or sensitivity, but the GFP-colS4 chimera protein was able to carry out specific detection of E. coli in drinking water samples in a procedure encompassing about 8 min for final result and this biosensor protein was able to detect in a linear way between 20 and 103 CFU of this bacterium. Below 20 CFU, the system cannot differentiate presence or absence of the target bacterium. The fluorescence in this biosensor system is provided by the GFP subunit of the chimeric protein, which, in the case of the better performing sensor bullet, GFP-colS4 chimera, is covalently bound to a flexible peptide bridge and to a bacteriocin binding specifically to E. coli cells. Once bound to the target bacteria, the excitation step with 395 nm LED light causes emission of fluorescence from the GFP domain, which is amplified in a photomultiplier tube, and finally this signal is converted into an output voltage which can be associated with a CFU value and these data distributed along mobile phone networks, for example. This method, and the portable fluorimeter which has been developed for it, may contribute to reduce the analysis time for detecting E. coli presence in drinking water.

摘要

从水源到通过管道输送,直至到达最终消费者或工业用户,饮用水都可能受到不同生物污染物的污染。其中一些是致病细菌和病毒,可能导致严重的胃肠道或全身性疾病。饮用水的微生物质量主要依赖于监测三种粪便来源的指示细菌,即大肠杆菌、粪肠球菌和产气荚膜梭菌,它们是人群潜在健康危害的早期哨兵。在此,我们描述了三种嵌合荧光蛋白弹头作为饮用水中大肠杆菌快速检测生物传感器候选物的分析。其中两种嵌合蛋白(基于绿色荧光蛋白 - 哈德鲁林和绿色荧光蛋白 - pb5嵌合蛋白)在特异性和/或灵敏度方面表现不佳,但绿色荧光蛋白 - colS4嵌合蛋白能够在约8分钟的流程内对饮用水样本中的大肠杆菌进行特异性检测并得出最终结果,这种生物传感器蛋白能够以线性方式检测该细菌20至10³CFU的数量。低于20CFU时,该系统无法区分目标细菌的存在与否。此生物传感器系统中的荧光由嵌合蛋白的绿色荧光蛋白亚基提供,在性能更佳的传感器弹头绿色荧光蛋白 - colS4嵌合蛋白中,绿色荧光蛋白亚基通过柔性肽桥与一种特异性结合大肠杆菌细胞的细菌素共价结合。一旦与目标细菌结合,用395nm发光二极管光激发会使绿色荧光蛋白结构域发出荧光,该荧光在光电倍增管中被放大,最后这个信号被转换为输出电压,该电压可以与CFU值相关联,例如这些数据可以通过移动电话网络进行传输。这种方法以及为此开发的便携式荧光计,可能有助于缩短检测饮用水中大肠杆菌存在情况的分析时间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d3c/5755745/7087fac8de07/pone.0184277.g001.jpg

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