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基于石墨相氮化碳的用于超灵敏检测鼠伤寒沙门氏菌的信号关闭比色和信号开启荧光双模式适体传感器。

Signal-off colorimetric and signal-on fluorometric dual-mode aptasensor for ultrasensitive detection of Salmonella Typhimurium using graphitic carbon nitride.

作者信息

Dang Thinh Viet, Jang In Seung, Nguyen Quynh Huong, Choi Hyeun Seok, Yu Byung Jo, Kim Moon Il

机构信息

Department of BioNano Technology, Gachon University, 1342 Seongnamdae-ro, Sujeong-gu, Seongnam, Gyeonggi 13120, Republic of Korea.

Low-Carbon Transition R&D Department, Research Institute of Sustainable Development Technology, Korea Institute of Industrial Technology (KITECH), Cheonan 31056, Republic of Korea.

出版信息

Food Chem. 2025 Feb 15;465(Pt 2):142176. doi: 10.1016/j.foodchem.2024.142176. Epub 2024 Nov 20.

Abstract

Food safety is severely burdened by the prevalence of foodborne pathogens and the diseases they cause, necessitating the development of rapid, easy-to-use, highly sensitive, and reliable detection methods. Here, a signal-off colorimetric and signal-on fluorometric dual-mode detection method for Salmonella Typhimurium (S. typhimurium) was developed based on its unique interaction with aptamer DNA and graphitic carbon nitride (GCN). In the absence of a target Salmonella species, 6-carboxyfluorescein (FAM)-labeled aptamers are adsorbed on the surface of GCN primarily via a π-π interaction, resulting in reduced fluorescence of FAM through GCN-mediated quenching as well as improved peroxidase-like activity of GCN to generate intense blue color through facilitated electrostatic attraction between the negatively charged aptamer and positively charged 3,3',5,5'-tetramethylbenzidine (TMB) substrate. The introduction of S. typhimurium to the sample solution causes the detachment of the aptamer from GCN due to its higher affinity for S. typhimurium than GCN, thereby rapidly reducing the colorimetric signal and recovering the fluorescence. We successfully determined the number of S. typhimurium using this method in a remarkably short duration (10-30 min), highlighting its rapidity. The limit of detection values for S. typhimurium were as low as 8 and 3 CFU/mL when using colorimetric and fluorometric methods, respectively. Moreover, this method can be used to detect S. typhimurium spiked in real vegetable extract and milk with high reproducibility and reliability. This method serves as a convenient route to the rapid, sensitive, selective, and reliable detection of pathogens from complex food samples, with the potential to replace conventional yet laborious methods currently in use.

摘要

食源性病原体的广泛存在及其引发的疾病给食品安全带来了沉重负担,因此需要开发快速、易用、高灵敏度且可靠的检测方法。在此,基于鼠伤寒沙门氏菌(Salmonella Typhimurium,简称S. typhimurium)与适配体DNA及石墨相氮化碳(GCN)的独特相互作用,开发了一种用于检测鼠伤寒沙门氏菌的比色信号关闭和荧光信号开启的双模式检测方法。在没有目标沙门氏菌的情况下,6-羧基荧光素(FAM)标记的适配体主要通过π-π相互作用吸附在GCN表面,导致FAM荧光通过GCN介导的猝灭而降低,同时GCN的类过氧化物酶活性提高,通过带负电荷的适配体与带正电荷的3,3',5,5'-四甲基联苯胺(TMB)底物之间的静电吸引增强而产生强烈的蓝色。将鼠伤寒沙门氏菌引入样品溶液中,由于其对鼠伤寒沙门氏菌的亲和力高于GCN,导致适配体从GCN上脱离,从而迅速降低比色信号并恢复荧光。我们使用该方法在极短的时间内(10 - 30分钟)成功测定了鼠伤寒沙门氏菌的数量,突出了其快速性。采用比色法和荧光法时,鼠伤寒沙门氏菌的检测限分别低至8和3 CFU/mL。此外,该方法可用于检测添加到真实蔬菜提取物和牛奶中的鼠伤寒沙门氏菌,具有高重现性和可靠性。该方法为从复杂食品样品中快速、灵敏、选择性和可靠地检测病原体提供了一条便捷途径,有潜力取代目前使用的传统且繁琐的方法。

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