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通过凝集素吸附亲和力阻抗对微生物进行识别和定量分析。

Microorganisms recognition and quantification by lectin adsorptive affinity impedance.

作者信息

Gamella M, Campuzano S, Parrado C, Reviejo A J, Pingarrón J M

机构信息

Dpto. Química Analítica, Universidad Complutense de Madrid, Madrid E-28040, Spain.

出版信息

Talanta. 2009 Jun 15;78(4-5):1303-9. doi: 10.1016/j.talanta.2009.01.059. Epub 2009 Feb 10.

DOI:10.1016/j.talanta.2009.01.059
PMID:19362192
Abstract

Lectin-based screen-printed gold electrodes are reported for the impedimetric label-free detection of bacteria. The selective interaction of lectins with carbohydrate components from microorganisms surface was used as the recognition principle for their detection and identification. Electrochemical impedance spectroscopy (EIS) was employed for the direct label-free transduction of the bacteria-lectin binding. Biotinylated Concanavalin A (Con A) and Escherichia coli were used for the evaluation of the lectin-bacteria complex formation. This complex was formed in solution, and then adsorbed onto the gold SPE surface. No bacteria immobilization was observed on the sensor prepared in the absence of ConA, demonstrating the absence of non-specific bacteria adsorption onto the gold SPE. On the contrary, the changes in electron transfer resistance allowed monitoring of E. coli-biotinylated Con A complex formation without any amplification step. Experimental variables such as the biotinylated-Con A concentration and the bacteria-lectin incubation time were optimized. The electron transfer resistance varied linearly with the logarithmic value of E. coli concentration over four orders of magnitude, 5.0 x 10(3) and 5.0 x 10(7) cfu mL(-1). The selectivity of the approach was evaluated by checking the impedimetric responses of gold SPE modified with the complexes formed between nine lectins and three different bacteria (E. coli, Staphylococcus aureus and Mycobacterium phlei). Different response profiles were found when the different lectins were used as recognition elements. principal component analysis (PCA) allowed classification and distinction among bacteria. Finally, electrochemical monitoring of beta-galactosidase activity for the surface attached bacteria was demonstrated to be useful to distinguish between E. coli and S. aureus, which exhibit a similar affinity towards biotinylated-Con A.

摘要

报道了基于凝集素的丝网印刷金电极用于细菌的无标记阻抗检测。凝集素与微生物表面碳水化合物成分的选择性相互作用被用作检测和鉴定细菌的识别原理。采用电化学阻抗谱(EIS)对细菌-凝集素结合进行直接无标记转换。生物素化的伴刀豆球蛋白A(Con A)和大肠杆菌用于评估凝集素-细菌复合物的形成。该复合物在溶液中形成,然后吸附到金SPE表面。在没有ConA的情况下制备的传感器上未观察到细菌固定,这表明金SPE上不存在非特异性细菌吸附。相反,电子转移电阻的变化允许在没有任何放大步骤的情况下监测大肠杆菌-生物素化Con A复合物的形成。对生物素化-Con A浓度和细菌-凝集素孵育时间等实验变量进行了优化。电子转移电阻在大肠杆菌浓度的四个数量级(5.0×10³和5.0×10⁷ cfu mL⁻¹)范围内与对数呈线性变化。通过检查用九种凝集素与三种不同细菌(大肠杆菌、金黄色葡萄球菌和草分枝杆菌)形成的复合物修饰的金SPE的阻抗响应来评估该方法的选择性。当使用不同的凝集素作为识别元件时,发现了不同的响应曲线。主成分分析(PCA)允许对细菌进行分类和区分。最后,对表面附着细菌的β-半乳糖苷酶活性进行电化学监测被证明有助于区分大肠杆菌和金黄色葡萄球菌,它们对生物素化-Con A表现出相似的亲和力。

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