优化双荧光分析研究AgNPs在大肠杆菌中的毒性。

Wei Hong, Shaopeng Chen
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引用次数: 1

摘要

银纳米颗粒(AgNPs)的不断增加的使用具有潜在的生态毒理学风险。为了进行全面的风险评估,大肠杆菌细胞被广泛使用,其中含有在lac启动子(lac::GFP)控制下组成表达GFP基因的质粒。流式细胞术是一种用于毒理学研究的先进技术,可对单个细胞进行快速、高效、多参数的分析。然而,由于纳米颗粒聚集的干扰,流式细胞术难以准确、灵敏地检测纳米颗粒的毒性。在该方案中,采用碘化丙啶(PI)-lac::GFP双荧光检测来确定AgNPs的毒性,并成功地将死亡或脆弱的细菌与活细菌和聚集的纳米颗粒区分开来。©2017 by John Wiley & Sons, Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Optimizing Dual Fluorescent Analysis to Investigate the Toxicity of AgNPs in E. coli.

The ever-increasing use of silver nanoparticles (AgNPs) carries potential ecotoxicological risks. For full risk assessment, E. coli cells harboring a plasmid with a constitutively expressed GFP gene under control of lac promoter (lac::GFP) are extensively utilized. Flow cytometry is an advanced technology usually applied to toxicological research for rapid, efficient, multi-parameter analysis of single cells. However, it is difficult to accurately and sensitively detect the toxicity of nanoparticles with flow cytometry due to the interference of aggregated nanoparticles. In this protocol, dual-fluorescence detection with a propidium iodide (PI)-lac::GFP assay is used to determine the toxicity of AgNPs and successfully discriminate the dead or fragilized bacteria from living bacteria and aggregated nanoparticles. © 2017 by John Wiley & Sons, Inc.

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