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Towards Multiplexed Bacteria Detection by Enzyme Responsive Hydrogels

机译:酶响应水凝胶对多重细菌检测

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In this work, patterned β-GUS sensing chitosan hydrogels functionalized with three different colorimetric substrates were fabricated for the multiplexed detection of the enzyme β-glucuronidase (β-GUS), which is secreted by >98% of all known Escherichia coli (E. coli) strains. The immobilization of fluorogenic and chromogenic substrates in specified areas allows a spatially resolved readout of the corresponding colorimetric signal. The apparent initial rate of the β-GUS induced cleavage of the reporter moieties of chitosan films functionalized with the chromogenic substrate 4-nitrophenyl-β-D-glucuronide (PNPG), the chromogenic substrate 5-bromo-4-chloro-3-indolyl-β-D-glucuronide (X-Gluc) and the fluorogenic substrate 4-methylumbelliferyl-β-D-glucuronide (MUG) were analyzed spectroscopically and confirmed a detectable reaction within less than 60 min. Likewise the released dyes were observed in the patterns owing to different colors by naked eye detection under appropriate illumination in less than 80 min. Hence the presence of a characteristic enzyme secreted by E. coli bacteria was successfully detected by three independent sensing moieties, which is important to reduce false positives by introducing redundancy. Patterned enzyme sensing chitosan hydrogels, which are functionalized with different substrates, open the possibility for multiplexed bacteria detection and in the long run also the identification of different bacteria strains.
机译:在这项工作中,制造用三种不同的比色基材官能化的图案化的β-GUS感测壳聚糖水凝胶用于复用检测酶β-葡糖醛酸酶(β-GUS),其被所有已知的大肠杆菌的> 98%分泌(E. Coli)菌株。在特定区域中的荧光和发色基质的固定允许在相应的比色信号的空间分辨读出。 β-GUS诱导与发色底物4-硝基苯基-β-D-葡糖醛酸(PNPG),发色底物5-溴-4-氯-3-吲哚基 - 吲哚基官能化壳聚糖膜的表观初始速率。分析光谱上,分析-β-D-葡糖醛酸酯(X-Gluc)和荧光底物4-甲基4-甲基葡萄糖蛋白酶(Mug),并在小于60分钟内确认可检测反应。同样,由于在不到80分钟的适当照射下,由于肉眼检测的不同颜色,在图案中观察到释放的染料。因此,通过三个独立的感测部分成功地检测到由大肠杆菌细菌分泌的特征酶的存在,这是通过引入冗余来降低误报的重要性。用不同底物官能化的图案化酶传感壳聚糖水凝胶,打开多重细菌检测的可能性,并且在长期的过程中也是不同的细菌菌株的鉴定。

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