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通过生物吸附激活纳米颗粒,用于检测牛奶和苹果汁中的大肠杆菌。

Activation of nanoparticles by biosorption for E. coli detection in milk and apple juice.

机构信息

Biotechnology Research Institute, National Research Council Canada, H4P 2R2 Montreal, Quebec, Canada.

出版信息

Appl Biochem Biotechnol. 2010 Sep;162(2):460-75. doi: 10.1007/s12010-009-8709-6. Epub 2009 Aug 1.

Abstract

Two types of silver nanoparticles were activated by specific sorption of biomolecules for the detection of Escherichia coli. The capture of this bacterium was performed using polyclonal antibodies (anti-E. coli) biosorbed onto nanospheres or nanorice through a protein-A layer. The bacterial detection was achieved using surface enhancement Raman scattering in order to compare the performance of these two nanoparticles. The activated silver nanospheres showed a better performance mainly due to the dimension of these nanoparticles. The detection limit has been established using the automated Raman mapping system. The technique was capable of detecting 10(3) cells/mL in milk and apple juice without any pre-enrichment. With an overall assay time less than 1 h, the process could be easily adapted to detect other pathogens by selecting the pertinent antibody. Furthermore, PCR was used for the DNA verification to assess whether the selected bacterial strain was identical before and after detection.

摘要

两种类型的银纳米粒子通过生物分子的特定吸附被激活,用于检测大肠杆菌。通过蛋白质 A 层将多克隆抗体(抗大肠杆菌)吸附到纳米球或纳米稻上,从而捕获这种细菌。使用表面增强拉曼散射来进行细菌检测,以比较这两种纳米粒子的性能。被激活的银纳米球表现出更好的性能,主要是由于这些纳米粒子的尺寸。使用自动化拉曼映射系统建立了检测下限。该技术能够在未经预富集的情况下检测到牛奶和苹果汁中的 10(3)个细胞/mL。整个检测时间不到 1 小时,该过程可以通过选择相关的抗体轻松适应检测其他病原体。此外,PCR 用于 DNA 验证,以评估所选细菌在检测前后是否相同。

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