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用于检测活的大肠杆菌O157:H7的无标记且无酶的灵敏荧光方法。

Label-free and enzyme-free sensitive fluorescent method for detection of viable Escherichia coli O157:H7.

作者信息

Chen Shujuan, Li Yongsheng, Fu Zhenzhen, Zeng Yue, He Li, Zhou Kang, Ao Xiaoling, Liu Shuliang, Zou Likou

机构信息

College of Food Science, Sichuan Agricultural University, Ya'an, 625014, PR China.

College of Forestry, Henan Agricultural University, Zhengzhou, 450000, PR China.

出版信息

Anal Biochem. 2018 Sep 1;556:145-151. doi: 10.1016/j.ab.2018.07.003. Epub 2018 Jul 7.

Abstract

We have developed a label-free, enzyme-free, modification-free and DNA extraction-free fluorescent aptasensing (LEFA) method for detection of E. coli O157:H7 based on G-quadruplex formation using two ingeniously designed hairpin probes (GHP1 and GHP2). In the presence of E. coli O157:H7, it released the single stranded initiation sequence (IS) resulting in the toehold strand displacement between GHP1 and GHP2, which in turn led to the cyclic reuse of the production of DNA assemblies with numerous G-quadruplex structures and initiation sequences. Then these G-quadruplex structures can be recognized quickly by N-methyl mesoporphyrin IX (NMM) resulting in significantly enhanced fluorescence. The LEFA method was successfully implemented for detecting E. coli O157:H7 with a detection limit of 66 CFU/mL in pure culture, 10 CFU/mL and 1 CFU/mL after pre-incubation of the milk and tap water for 4 and 8 h, respectively. Moreover, the strategy could distinguish viable E. coli O157:H7 from dead E. coli O157:H7 and other species of pathogen cells. Furthermore, the whole process of the strategy is accomplished within 100 min. The results indicated that the approach may be used to effectively control potential microbial hazards in human health, food safety, and animal husbandry.

摘要

我们开发了一种基于G-四链体形成的无标记、无酶、无修饰且无需DNA提取的荧光适体传感(LEFA)方法,用于检测大肠杆菌O157:H7,该方法使用了两个精心设计的发夹探针(GHP1和GHP2)。在大肠杆菌O157:H7存在的情况下,它释放出单链起始序列(IS),导致GHP1和GHP2之间发生链置换引发,进而导致具有大量G-四链体结构和起始序列的DNA组装产物的循环再利用。然后,这些G-四链体结构可以被N-甲基中卟啉IX(NMM)快速识别,从而使荧光显著增强。LEFA方法成功用于检测大肠杆菌O157:H7,在纯培养物中的检测限为66 CFU/mL,牛奶和自来水分别预孵育4小时和8小时后的检测限为10 CFU/mL和1 CFU/mL。此外,该策略可以区分活的大肠杆菌O157:H7和死的大肠杆菌O157:H7以及其他病原体细胞种类。此外,该策略的整个过程在100分钟内完成。结果表明,该方法可用于有效控制人类健康、食品安全和畜牧业中的潜在微生物危害。

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