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Fluorometric Aptasensor for Determination of Escherichia coli O157:H7 by FRET Effect between Aminated Carbon Quantum Dots and Graphene Oxide

机译:荧光致动体测定,用于测定胺化碳量子点和氧化石墨烯与摩托效应的摩托效应

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A fluorometric aptasensor based on Escherichia coli O157:H7 (E. coli O157:H7) aptamer labeled aminated carbon quantum dots (NH_(2)-CQDs) and graphene oxide (GO) for the determination of E. coli O157:H7 was developed. In this research, carboxyl group (–COOH) terminated E. coli O157:H7 aptamer was steadily labeled to NH_(2)-CQDs by amidation reaction, and played the role of energy donor and was responsible for chemical recognition. Correspondingly, GO served as an energy acceptor. The introduction of NH_(2)-CQDs not only made the aptamer bond stably through covalent bond, but also significantly enhanced the fluorescence intensity compared with general CQDs. The NH_(2)-CQDs-aptamer is adsorbed on the surface of GO through π-π stacking and hydrophobic interaction. The fluorescence of NH_(2)-CQDs-aptamer was quenched via fluorescence resonance energy transfer (FRET) between NH_(2)-CQDs and GO. After adding E. coli O157:H7, the specific binding affinity between NH_(2)-CQDs-aptamer and E. coli O157:H7 lead to desorption of NH_(2)-CQDs-aptamer from GO, and recovery of the fluorescence intensity of NH_(2)-CQDs-aptamer. Under the optimal conditions, the increased fluorescence intensity showed a good linear relationship to concentrations of E. coli O157:H7 in the range 10~(2) – 10~(7) cells/mL, with a detection limit of 89 cells/mL. Furthermore, the developed method was successfully applied to the determination of E. coli O157:H7 in commercial milk samples.
机译:基于大肠杆菌O157:H7(Coli O157:H7)适体标记胺化碳量子点(NH_(2)-CQDS)和石墨烯氧化物(GO)的氧化物氧化物(GO)的测定以确定 e。 Coli O157:H7是开发的。在该研究中,羧基(-COOH)终止了 e。 Coli O157:H7 Aptamer通过酰胺化反应稳定地标记为NH_(2)-CQDS,并发挥了能量供体的作用,并负责化学识别。相应地,担任能量受体。 NH_(2)-CQDS的引入不仅通过共价键稳定地使适体键合,而且与一般CQD相比,也显着提高了荧光强度。 NH_(2)-cqds-aptamer吸附在通过π-π堆叠和疏水相互作用的表面上。通过NH_(2)-CQDS之间的荧光共振能量转移(FRET)淬灭NH_(2)-CQDS-APTamer的荧光并进行。添加 e后。 COLI O157:H7,NH_(2)-CQDS-适体和 E之间的特异结合亲和力。 COLI O157:H7从去的GO开始并从GO开始解吸NH_(2)-CQDS-APTamer,并恢复NH_(2)-CQDS-APTamer的荧光强度。在最佳条件下,增加的荧光强度显示出与浓度的良好的线性关系。 COLI O157:H7在10〜(2) - 10〜(7)个细胞/ mL的范围内,检测限为89个细胞/ mL。此外,成功地应用于e> e的确定方法。 Coli O157:H7在商业牛奶样品中。

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