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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >A novel magneto-DNA duplex probe for bacterial DNA detection based on exonuclease III-aided cycling amplification
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A novel magneto-DNA duplex probe for bacterial DNA detection based on exonuclease III-aided cycling amplification

机译:基于核酸外切酶III辅助循环扩增的新型磁性DNA双链探针用于细菌DNA检测

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摘要

A novel magneto-DNA duplex probe for bacterial DNA detection based on exonuclease HI (Exo-III) aided cycling amplification has been developed. This magneto-DNA duplex probe contains a partly hybrid fluorophore-modified capture probe and a fluorophore-modified signal probe with magnetic microparticle as carrier. In the presence of a perfectly matched target bacterial DNA, blunt 3'-terminus of the capture probe is formed, activating the Exo-III aided cycling amplification. Thus, Exo-III catalyzes the stepwise removal of mononucleotides from this terminus, releasing both fluorophore-modified signal probe, fluorescent dyes of the capture probe and target DNA. The released target DNA then starts a new cycle, while released fluorescent fragments are recovered with magnetic separation for fluorescence signal collection. This system exhibited sensitive detection of bacterial DNA, with a detection limit of 14 pM because of the unique cleavage function of Exo-III, high fluorescence intensity, and separating function of magneto-DNA duplex probes. Besides this sensitivity, this strategy exhibited excellent selectivity with mismatched bacterial DNA targets and other bacterial species targets and good applicability in real seawater samples, hence, this strategy could be potentially used for qualitative and quantitative analysis of bacteria. (C) 2014 Elsevier B.V. All rights reserved.
机译:基于核酸外切酶HI(Exo-III)辅助循环扩增的新型细菌DNA DNA探针检测技术已经开发出来。该磁性DNA双链体探针包含部分杂交的荧光团修饰的捕获探针和以磁性微粒为载体的荧光团修饰的信号探针。在完美匹配的目标细菌DNA的存在下,形成了捕获探针的钝3'-末端,激活了Exo-III辅助的循环扩增。因此,Exo-III催化从该末端逐步去除单核苷酸,从而释放出荧光团修饰的信号探针,捕获探针的荧光染料和目标DNA。然后释放的靶DNA开始新的循环,同时释放的荧光片段通过磁分离回收,以收集荧光信号。由于Exo-III的独特切割功能,高荧光强度和磁DNA双工探针的分离功能,该系统对细菌DNA的检测灵敏度很高,检测限为14 pM。除了这种敏感性外,该策略还对错配的细菌DNA靶标和其他细菌物种靶标表现出优异的选择性,并且在实际的海水样品中具有良好的适用性,因此,该策略可潜在地用于细菌的定性和定量分析。 (C)2014 Elsevier B.V.保留所有权利。

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