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微流控中的大肠杆菌和巴斯德毕赤酵母的声致发光。

Sonolysis of Escherichia coli and Pichia pastoris in microfluidics.

机构信息

Institute of High Performance Computing, Singapore.

出版信息

Lab Chip. 2012 Feb 21;12(4):780-6. doi: 10.1039/c2lc20861j. Epub 2011 Dec 20.

Abstract

We report on an efficient ultrasound based technique for lysing Escherichia coli and Pichia pastoris with oscillating cavitation bubbles in an integrated microfluidic system. The system consists of a meandering microfluidic channel and four piezoelectric transducers mounted on a glass substrate, with the ultrasound exposure and gas pressure regulated by an automatic control system. Controlled lysis of bacterial and yeast cells expressing green fluorescence protein (GFP) is studied with high-speed photography and fluorescence microscopy, and quantified with real-time polymerase chain reaction (qRT-PCR) and fluorescence intensity. The effectiveness of cell lysis correlates with the duration of ultrasound exposure. Complete lysis can be achieved within one second of ultrasound exposure with a temperature increase of less than 3.3 °C. The rod-shaped E. coli bacteria are disrupted into small fragments in less than 0.4 seconds, while the more robust elliptical P. pastoris yeast cells require around 1.0 second for complete lysis. Fluorescence intensity measurements and qRT-PCR analysis show that functionality of GFP and genomic DNA for downstream analytical assays is maintained.

摘要

我们报告了一种基于超声的高效技术,用于在集成微流控系统中通过振荡空化气泡裂解大肠杆菌和巴斯德毕赤酵母。该系统由蜿蜒微流道和安装在玻璃基底上的四个压电换能器组成,通过自动控制系统调节超声辐射和气压。通过高速摄影和荧光显微镜研究了表达绿色荧光蛋白 (GFP) 的细菌和酵母细胞的受控裂解,并通过实时聚合酶链反应 (qRT-PCR) 和荧光强度进行了定量。细胞裂解的有效性与超声辐射的持续时间相关。在温度升高小于 3.3°C 的情况下,仅需 1 秒的超声辐射即可实现完全裂解。杆状大肠杆菌细菌在不到 0.4 秒的时间内被分解成小碎片,而更坚固的椭圆形巴斯德毕赤酵母细胞则需要大约 1.0 秒才能完全裂解。荧光强度测量和 qRT-PCR 分析表明,GFP 的功能和基因组 DNA 可用于下游分析检测。

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