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Selective Discrimination of Key Enzymes of Pathogenic and Nonpathogenic Bacteria on Autonomously Reporting Shape-Encoded Hydrogel Patterns

机译:对致病性和非致病菌的关键酶选择性辨别在自主报告形状编码水凝胶模式中的关键酶

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This work reports on a new approach to rapidly and selectively detect and discriminate enzymes of pathogenic from those of nonpathogenic bacteria using a patterned autonomously reporting hydrogel on a transparent support, in which the selectivity has been encoded by the pattern shape to enable facile detection by a color change at one single wavelength. In particular, enzyme-responsive chitosan hydrogel layers that report the presence of the enzymes beta-glucuronidase (beta-Gus) and beta-galactosidase (beta-Gal), produced by the nonvirulent Escherichia coli K12 and the food-borne biosafety level 3 pathogen enterohemorrhagic E. coli, respectively, via the blue color of an indigo dye were patterned by two complementary strategies. The comparison of the functionalization of patterned chitosan patches on a solid support with two chromogenic substrates on one hand and the area-selective conjugation of the substrates on the other hand showed that the two characteristic enzymes could indeed be rapidly and selectively discriminated. The limits of detection of the highly stable sensing layers for an observation time of 60 min using a spectrophotometer correspond to enzyme concentrations of beta-Gus and beta-Gal of = 5 and = 3 nM, respectively, and to = 62 and = 33 nM for bare eye detection in nonoptimized sensor patches. These results confirm the applicability of this approach, which is compatible with the simple measurement of optical density at one single wavelength only as well as with parallel, multiplexed detection, to differentiate the enzymes secreted by a highly pathogenic E. coli from a nonpathogenic E. coli on the basis of specifically secreted enzymes. Hence, a general approach for the rapid and selective detection of enzymes of different bacterial species for potential applications in food safety as well as point-of-care microbiological diagnostics is described.
机译:这项工作报告了使用在透明支撑的透明支撑件上的图案自主报告水凝胶快速和选择性地检测和区分病原菌的致病菌的酶,其中选择性已经通过图案形状进行了编码,以便通过a颜色在一个单一波长处变化。特别是,通过非致者大肠杆菌K12和食品传播的生物安全级3病原体,报告酶响应壳聚糖层,其报告酶β-葡萄糖醛酸酯酶(Beta-Gus)和β-半乳糖苷酶(Beta-Gal)的存在。通过两种互补策略,分别通过靛蓝染料的蓝色分别通过两种互补策略进行肠内鼠髓大肠杆菌。一方面用两种发色基质的固体载体对具有两种发色基质的固体载体的官能化的比较及另一方面的基板的面积选择性缀合显示,两只特征酶确实可以快速和选择性地区分。使用分光光度计检测60分钟的观察时间的高稳定感测层的极限对应于β-GUS和β-GA1的酶浓度,分别是β-β-β-β-β-β-β-β-β-β-β-β-β-β-β-β-β-β-β-β-β-β-1。对于非优化传感器贴片中的裸眼检测,= 62和& 33 nm。这些结果证实这种方法,它与光密度中的一个单一波长的简单测量兼容的适用性唯一以及具有平行,多重检测,以区别于非致病性大肠杆菌由高度病原性大肠杆菌分泌的酶基于特异性分泌酶的大肠杆菌。因此,描述了一种用于快速和选择性检测不同细菌物种酶的潜在食品安全应用以及护理点微生物诊断方法的一般方法。

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