Accessing DNA by low voltage alternating current Joule effect heating
Accessing DNA by low voltage alternating current Joule effect heating
A DNA release sample preparation method based on the use! of low voltage alternating currents (LVACs) to generate Joule effect heating (JEH) is reported. This is a simple cell disruption strategy that offers internal, homogenous, rapid and low power consumption heating for the access of analytical grade DNA in seconds. A 100 muL JEH microreactor with a parallel and symmetric two electrode arrangement for uniform field generation was fabricated by machining and used to characterise JEH and DNA release from human epithelia, yeast (Saccharomyces cerevisiae) and Gram-positive bacteria (Enterococcus faecium) cell types. A 1 kHz sinusoidal low voltage (e.g. 10 Vrms) alternating current was used to reduce electrode: sample interactions. Following 96degreesC JEH treatment, effective DNA release was identified by PicoGreen(R) quantification for all three cell types. The JEH treated sample material was further successfully used, without purification, as a PCR template. Exposure to JEH-mediated 96degreesC temperatures for a 1 s duration was used to provide PCR-grade DNA template material from S. cerevisiae and E. faecium cells, and a 10 s duration was used for human epithelia cells. However, prolonged (> 1 min) exposure to 96degreesC JEH-mediated temperatures resulted in diminished DNA returns and the production of components that interfered with the PCR reaction. Further miniaturisation of the LVAC JEH cell by microfabtication was considered, and a JEH microreactor designs were evaluated by FLOTHERM v3.2 thermal modelling. Thermal isolation, using a free-standing cavity structure was identified as an excellent means to enable rapid heating (220degreesC s(-1)) with low power consumption (0.2 W).
genetic analysis, sample preparation, dna extraction, joule effect heating, microreactor, amplification, pcr, microorganisms, systems, chips
1-12
West, Jonathan
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Hurley, Eileen
847c2d9f-b1e7-4b88-8cf2-b48079591562
Cordero, Nicolás
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Collins, John K.
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Lane, William
ff300c43-4d91-4da7-8f9a-c0787966f7d3
Berney, Helen
4bff1286-8f87-4999-a9db-a52b6a20def7
24 November 2004
West, Jonathan
f1c2e060-16c3-44c0-af70-242a1c58b968
Hurley, Eileen
847c2d9f-b1e7-4b88-8cf2-b48079591562
Cordero, Nicolás
4e891f1b-5e5f-4b1a-a713-1f3c78ee90c1
Collins, John K.
9abadce2-a040-4f34-a91f-7a43a5deda7a
Lane, William
ff300c43-4d91-4da7-8f9a-c0787966f7d3
Berney, Helen
4bff1286-8f87-4999-a9db-a52b6a20def7
West, Jonathan, Hurley, Eileen, Cordero, Nicolás, Collins, John K., Lane, William and Berney, Helen
(2004)
Accessing DNA by low voltage alternating current Joule effect heating.
Analytica Chimica Acta, 527 (1), .
Abstract
A DNA release sample preparation method based on the use! of low voltage alternating currents (LVACs) to generate Joule effect heating (JEH) is reported. This is a simple cell disruption strategy that offers internal, homogenous, rapid and low power consumption heating for the access of analytical grade DNA in seconds. A 100 muL JEH microreactor with a parallel and symmetric two electrode arrangement for uniform field generation was fabricated by machining and used to characterise JEH and DNA release from human epithelia, yeast (Saccharomyces cerevisiae) and Gram-positive bacteria (Enterococcus faecium) cell types. A 1 kHz sinusoidal low voltage (e.g. 10 Vrms) alternating current was used to reduce electrode: sample interactions. Following 96degreesC JEH treatment, effective DNA release was identified by PicoGreen(R) quantification for all three cell types. The JEH treated sample material was further successfully used, without purification, as a PCR template. Exposure to JEH-mediated 96degreesC temperatures for a 1 s duration was used to provide PCR-grade DNA template material from S. cerevisiae and E. faecium cells, and a 10 s duration was used for human epithelia cells. However, prolonged (> 1 min) exposure to 96degreesC JEH-mediated temperatures resulted in diminished DNA returns and the production of components that interfered with the PCR reaction. Further miniaturisation of the LVAC JEH cell by microfabtication was considered, and a JEH microreactor designs were evaluated by FLOTHERM v3.2 thermal modelling. Thermal isolation, using a free-standing cavity structure was identified as an excellent means to enable rapid heating (220degreesC s(-1)) with low power consumption (0.2 W).
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Published date: 24 November 2004
Keywords:
genetic analysis, sample preparation, dna extraction, joule effect heating, microreactor, amplification, pcr, microorganisms, systems, chips
Organisations:
Cancer Sciences
Identifiers
Local EPrints ID: 346431
URI: http://eprints.soton.ac.uk/id/eprint/346431
ISSN: 0003-2670
PURE UUID: ad42ff0e-8b89-4cda-bef5-1eb7521f23ab
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Date deposited: 26 Feb 2013 13:56
Last modified: 08 Jan 2022 03:17
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Contributors
Author:
Eileen Hurley
Author:
Nicolás Cordero
Author:
John K. Collins
Author:
William Lane
Author:
Helen Berney
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