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聚合酶链反应与α-溶血素纳米孔相结合检测烟草青枯病

Detection of Tobacco Bacterial Wilt Caused by by Combining Polymerase Chain Reaction with an α-Hemolysin Nanopore.

作者信息

Wang Ying, Li Yusen, Zhou Xin, Zhang Wenna, Zhang Shusheng, Xi Dongmei

机构信息

Shandong Provincial Key Laboratory of Detection Technology for Tumor Markers, College of Life Science, Linyi University, Linyi 276005, China.

Shandong (Linyi) Institute of Modern Agriculture, Zhejiang University, Linyi 276000, China.

出版信息

Nanomaterials (Basel). 2023 Jan 13;13(2):332. doi: 10.3390/nano13020332.

Abstract

Tobacco bacterial wilt is a serious disease caused by the soil-borne bacterium (). Herein, a rapid and purification-free α-hemolysin (α-HL) nanopore-sensing strategy based on polymerase chain reaction (PCR) and lambda exonuclease digestion was established to detect . A 198-nucleotide-long single-stranded DNA was obtained via asymmetric PCR or the lambda exonuclease-mediated digestion of the PCR product. The DNA fragment produced unique long-lived, current-blocking signals when it passed through the α-HL nanopore. This sensing approach can allow for the determination of in tobacco samples and can be conveniently extended to other DNA monitoring because of the extremely wide range of PCR applications.

摘要

烟草青枯病是由一种土壤传播细菌()引起的严重病害。在此,基于聚合酶链反应(PCR)和λ外切核酸酶消化建立了一种快速且无需纯化的α-溶血素(α-HL)纳米孔传感策略来检测(该细菌)。通过不对称PCR或PCR产物的λ外切核酸酶介导消化获得了一条198个核苷酸长的单链DNA。当该DNA片段通过α-HL纳米孔时会产生独特的长寿命电流阻断信号。由于PCR应用范围极其广泛,这种传感方法能够用于测定烟草样品中的(该细菌),并且可以方便地扩展到其他DNA监测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5e7/9863824/7a4535907aca/nanomaterials-13-00332-sch001.jpg

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