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Ultrasensitive Electrochemical Biosensor for Detection of DNA from Bacillus subtilis by Coupling Target-Induced Strand Displacement and Nicking Endonuclease Signal Amplification

机译:通过耦合目标诱导的链置换和尼克核酸内切酶信号放大检测枯草芽孢杆菌DNA的超灵敏电化学生物传感器

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摘要

A simple, ultrasensitive, and specific electrochemical biosensor was designed to determine the given DNA sequence of Bacillus subtilis by coupling target-induced strand displacement and nicking endonuclease signal amplification. The target DNA (TD, the DNA sequence from the hypervarient region of 16S rDNA of Bacillus subtilis) could be detected by the differential pulse voltammetry (DPV) in a range from 0.1 fM to 20 fM with the detection limit down to 0.08 fM at the 3s_(blank) level. This electrochemical biosensor exhibits high distinction ability to single-base mismatch, double-bases mismatch, and noncomplementary DNA sequence, which may be expected to detect single-base mismatch and single nucleotide polymorphisms (SNPs). Moreover, the applicability of the designed biosensor for detecting the given DNA sequence from Bacillus subtilis was investigated. The result obtained by electrochemical method is approximately consistent with that by a real-time quantitative polymerase chain reaction detecting system (QPCR) with SYBR Green.
机译:设计了一种简单,超灵敏,特异的电化学生物传感器,通过偶联靶标诱导的链置换和切口内切核酸酶信号放大来确定枯草芽孢杆菌的给定DNA序列。可以通过差分脉冲伏安法(DPV)检测目标DNA(TD,来自枯草芽孢杆菌16S rDNA高变区的DNA序列),检测范围为0.1 fM至20 fM,检测限在200 nm时降至0.08 fM。 3s_(空白)级别。这种电化学生物传感器对单碱基错配,双碱基错配和非互补DNA序列表现出很高的区分能力,有望检测到单碱基错配和单核苷酸多态性(SNP)。此外,研究了所设计的生物传感器从枯草芽孢杆菌检测给定DNA序列的适用性。电化学方法获得的结果与带有SYBR Green的实时定量聚合酶链反应检测系统(QPCR)的结果基本一致。

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