Sonolysis of Escherichia coli and Pichia pastoris in microfluidics

被引:46
作者
Tandiono, Tandiono [1 ]
Ow, Dave Siak-Wei [2 ]
Driessen, Leonie [3 ]
Chin, Cara Sze-Hui [2 ]
Klaseboer, Evert [1 ]
Choo, Andre Boon-Hwa [2 ]
Ohl, Siew-Wan [1 ]
Ohl, Claus-Dieter [3 ]
机构
[1] Inst High Performance Comp, Singapore 138632, Singapore
[2] Bioproc Technol Inst, Singapore 138668, Singapore
[3] Nanyang Technol Univ, Sch Phys & Math Sci, Div Phys & Appl Phys, Singapore 637371, Singapore
关键词
CELL-LYSIS; HETEROLOGOUS PROTEINS; LATEST DEVELOPMENTS; COPY-NUMBER; DEVICE; WALL; EXTRACTION; EXPRESSION;
D O I
10.1039/c2lc20861j
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
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 degrees 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.
引用
收藏
页码:780 / 786
页数:7
相关论文
共 29 条
[21]   EXTRACTION, PURIFICATION AND PROPERTIES OF AEQUORIN, A BIOLUMINESCENT PROTEIN FROM LUMINOUS HYDROMEDUSAN, AEQUOREA [J].
SHIMOMURA, O ;
JOHNSON, FH ;
SAIGA, Y .
JOURNAL OF CELLULAR AND COMPARATIVE PHYSIOLOGY, 1962, 59 (03) :223-&
[22]   Determination of yeast cell wall thickness and cell diameter using new methods [J].
Srinorakutara, T .
JOURNAL OF FERMENTATION AND BIOENGINEERING, 1998, 86 (03) :253-260
[23]   Sonochemistry and sonoluminescence in microfluidics [J].
Tandiono ;
Ohl, Siew-Wan ;
Ow, Dave S. W. ;
Klaseboer, Evert ;
Wong, Victor V. ;
Dumke, Rainer ;
Ohl, Claus-Dieter .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (15) :5996-5998
[24]   Creation of cavitation activity in a microfluidic device through acoustically driven capillary waves [J].
Tandiono ;
Ohl, Siew-Wan ;
Ow, Dave Siak-Wei ;
Klaseboer, Evert ;
Wong, Victor V. T. ;
Camattari, Andrea ;
Ohl, Claus-Dieter .
LAB ON A CHIP, 2010, 10 (14) :1848-1855
[25]   Lysing bacterial spores by sonication through a flexible interface in a microfluidic system [J].
Taylor, MT ;
Belgrader, P ;
Furman, BJ ;
Pourahmadi, F ;
Kovacs, GTA ;
Northrup, MA .
ANALYTICAL CHEMISTRY, 2001, 73 (03) :492-496
[26]   The green fluorescent protein [J].
Tsien, RY .
ANNUAL REVIEW OF BIOCHEMISTRY, 1998, 67 :509-544
[27]   A microfluidic flow-through device for high throughput electrical lysis of bacterial cells based on continuous dc voltage [J].
Wang, Hsiang-Yu ;
Bhunia, Arun K. ;
Lu, Chang .
BIOSENSORS & BIOELECTRONICS, 2006, 22 (05) :582-588
[28]   Effects of the presence of CoIEI plasmid DNA in Escherichia coli on the host cell metabolism [J].
Wang, Zhijun ;
Li Xiang ;
Shao, Junjie ;
Wegrzyn, Alicja ;
Wegrzyn, Grzegorz .
MICROBIAL CELL FACTORIES, 2006, 5 (1)
[29]   Microchip device for cell lysis, multiplex PCR amplification, and electrophoretic sizing [J].
Waters, LC ;
Jacobson, SC ;
Kroutchinina, N ;
Khandurina, J ;
Foote, RS ;
Ramsey, JM .
ANALYTICAL CHEMISTRY, 1998, 70 (01) :158-162