Characterization of the synthetic compatible solute homoectoine as a potent PCR enhancer

被引:82
作者
Schnoor, M
Voss, P
Cullen, P
Böking, T
Galla, HJ
Galinski, EA
Lorkowski, S [1 ]
机构
[1] Univ Munster, Inst Arteriosclerosis Res, D-4400 Munster, Germany
[2] Univ Munster, Inst Biochem, D-4400 Munster, Germany
[3] Ogham GmbH, Munster, Germany
[4] Univ Bonn, Dept Microbiol & Biotechnol, D-5300 Bonn, Germany
关键词
compatible solutes; PCR enhancer; homoectoine; betaine; DNA melting;
D O I
10.1016/j.bbrc.2004.07.200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Different substances such as dimethyl sulfoxide, tetramethylene sulfoxide, 2-pyrollidone, and the naturally occurring compatible solute betaine enhance PCR amplification of GC-rich DNA templates with high melting temperatures. In particular, cyclic compatible solutes outperform traditional PCR enhancers. We therefore investigated the effects that cyclic naturally occurring ectoine-type compatible solutes and their synthetic derivatives have on melting temperature of double-stranded DNA (dsDNA) and on PCR amplification of different templates. L-Ectoine, betaine, and derivatives Of L-ectoine decreased, whereas beta-hydroxyectoine increased, the melting temperature of dsDNA. The ability to decrease the melting temperature was greatest for homoectoine, a new synthetic derivative Of L-ectoine. Furthermore, compatible solutes, especially homoectoine, enhanced PCR amplification of GC-rich DNA (72.6% GC content; effective range: 0.1-0.5 M). (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:867 / 872
页数:6
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