溶解
毕赤酵母
大肠杆菌
微流控
荧光
荧光显微镜
绿色荧光蛋白
酵母
化学
细菌
生物物理学
超声波
生物
分子生物学
纳米技术
生物化学
材料科学
重组DNA
光学
物理
遗传学
基因
声学
作者
Tandiono Tandiono,Dave Siak‐Wei Ow,Leonie M. A. Driessen,Cara Sze-Hui Chin,Evert Klaseboer,Andre Choo,Siew‐Wan Ohl,Claus‐Dieter Ohl
出处
期刊:Lab on a Chip
[Royal Society of Chemistry]
日期:2011-12-20
卷期号:12 (4): 780-786
被引量:56
摘要
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.
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