Real-time quantitative LAMP (loop-mediated isothermal amplification of DNA) as a simple method for monitoring ammonia-oxidizing bacteria

被引:84
作者
Aoi, Yoshiteru [1 ]
Hosogai, Mariko [1 ]
Tsuneda, Satoshi [1 ]
机构
[1] Waseda Univ, Dept Chem Engn, Shinjuku Ku, Tokyo 1698555, Japan
关键词
LAMP (loop-mediated isothermal amplification of DNA); Quantification; amoA gene;
D O I
10.1016/j.jbiotec.2006.04.007
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Loop-mediated isothermal amplification (LAMP) of DNA is a novel technique for the amplification of DNA under isothermal conditions. For the first time, we applied this method to develop a simple and quantitative monitoring method for environmental microorganisms targeting amoA gene in ammonia-oxidizing bacteria. Quantitative analysis was performed first by measuring fluorescence derived from an intercalation dye using a real-time thermal cycler, and then by measuring the turbidity of the reaction solution using a real-time turbidimeter. As a result, it was possible to quantify the initial amoA DNA concentration from an environment with a sensitivity down to 10(2) DNA copies of target DNA and a dynamic range of 7-9 orders in magnitude. Background DNA from nontargeted bacteria (Pseudomonas denitrificans) that does not encode amoA gene did not affect the quantitative capability of LAMP. Over results suggested that the real-time LAMP is effective for monitoring microorganisms and their gene expression in environments. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:484 / 491
页数:8
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