Miniaturized bacterial biosensor system for arsenic detection holds great promise for making integrated measurement device.

Nina Buffi, Davide Merulla, Julien Beutier, Fanny Barbaud, Siham Beggah, Harald van Lintel, Philippe Renaud, Jan Roelof van der Meer
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引用次数: 12

Abstract

Combining bacterial bioreporters with microfluidics systems holds great promise for in-field detection of chemical or toxicity targets. Recently we showed how Escherichia coli cells engineered to produce a variant of green fluorescent protein after contact to arsenite and arsenate can be encapsulated in agarose beads and incorporated into a microfluidic chip to create a device for in-field detection of arsenic, a contaminant of well known toxicity and carcinogenicity in potable water both in industrialized and developing countries. Cell-beads stored in the microfluidics chip at -20°C retained inducibility up to one month and we were able to reproducibly discriminate concentrations of 10 and 50 μg arsenite per L (the drinking water standards for European countries and the United States, and for the developing countries, respectively) from the blank in less than 200 minutes. We discuss here the reasons for decreasing bioreporter signal development upon increased storage of cell beads but also show how this decrease can be reduced, leading to a faster detection and a longer lifetime of the device.

小型化的细菌生物传感器砷检测系统在制作集成测量装置方面具有广阔的应用前景。
将细菌生物报告器与微流体系统相结合,对化学或毒性目标的现场检测具有很大的希望。最近,我们展示了如何将大肠杆菌细胞在接触亚砷酸盐和砷酸盐后产生一种绿色荧光蛋白的变异,并将其封装在琼脂糖珠中,并将其放入微流控芯片中,以创建一种现场检测砷的装置,砷是一种在工业化国家和发展中国家的饮用水中众所周知的毒性和致癌性污染物。在-20°C下储存在微流体芯片中的细胞珠保持诱导性长达一个月,我们能够在不到200分钟的时间内从空白中重复性地区分浓度为每升10和50 μg的亚砷酸盐(分别为欧洲国家和美国以及发展中国家的饮用水标准)。我们在这里讨论了在增加细胞珠储存时减少生物报告信号发展的原因,但也显示了如何减少这种减少,从而导致更快的检测和更长的设备寿命。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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