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一种用于从具有临床意义的病原体中提取基因组细菌DNA的简单且经济的保存方法。

A simple and economic preservation method for genomic bacterial DNA from clinically significant pathogens.

作者信息

Moore John E, Xu Jiru, Millar B Cherie

机构信息

Northern Ireland Public Health Laboratory, Department of Bacteriology, Belfast City Hospital, Lisburn Road, Belfast BT9 7AD, Northern Ireland, United Kingdom.

出版信息

J Microbiol Methods. 2005 Jan;60(1):131-3. doi: 10.1016/j.mimet.2004.09.007.

DOI:10.1016/j.mimet.2004.09.007
PMID:15567233
Abstract

Bacterial culture was allowed to dry to completeness on Columbia agar base with defibrinated horse blood. Following 6 months storage at room temperature, microbial DNA was extracted and successfully amplified by PCR. This storage technique has the advantage over other methods of not requiring (i) a DNA extraction protocol prior to storage and (ii) refrigeration and/or freezing. This technique maybe useful in the transportation of bacterial genomic DNA in nonviable cells as well as reliable method for the storage of DNA in underdeveloped countries.

摘要

将细菌培养物接种在含去纤维马血的哥伦比亚琼脂培养基上,使其完全干燥。在室温下储存6个月后,提取微生物DNA,并通过聚合酶链反应(PCR)成功扩增。与其他方法相比,这种储存技术的优势在于:(i)储存前无需DNA提取方案;(ii)无需冷藏和/或冷冻。该技术可能有助于在不发达国家非存活细胞中运输细菌基因组DNA,也是一种可靠的DNA储存方法。

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