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使用 Chelex-100 微波法在 20 分钟内纯化细菌基因组 DNA:来自土壤样本中分离的乳酸菌菌株的实例。

Purification of bacterial genomic DNA in less than 20 min using chelex-100 microwave: examples from strains of lactic acid bacteria isolated from soil samples.

机构信息

Centro de Investigación y Asistencia en Tecnología y Diseño del Estado de Jalisco, Colonia García Gineres, Mérida, Yucatán, México.

出版信息

Antonie Van Leeuwenhoek. 2010 Nov;98(4):465-74. doi: 10.1007/s10482-010-9462-0. Epub 2010 Jun 17.

Abstract

We established a Chelex 100-Microwave method for the purification of bacterial genomic DNA (gDNA) in less than 20 min with high yield and good quality, useful for multiple purposes. It combines Chelex 100, proteinase K, RNase A and heating in a microwave oven. The resulting gDNA was used directly to identify bacterial species of the Order Lactobacillales by means of PCR amplification of their 16S rDNA gene, isolated from sediments on the Yucatan Peninsula, Mexico. This method produced gDNA free of phenolic and protein residual contaminants from 100 of these isolated bacteria. 16S rDNA amplification and sequencing showed Pediococcus acidilactici to prevail in inland lagoons, and Pediococcus pentosaceus, Lactobacillus plantarum, Lactobacillus sp., and Lactobacillus fermentum to be most abundant in the soils of livestock farms. The combination of Chelex 100, enzymes and microwave heating used in the Chelex 100-Microwave method produced large amounts of highly pure gDNA from Gram-positive and Gram-negative bacteria, in less than 20 min.

摘要

我们建立了一种 Chelex 100-微波法,用于在不到 20 分钟的时间内从革兰氏阳性和革兰氏阴性细菌中提取高产且高质量的细菌基因组 DNA(gDNA),适用于多种用途。该方法结合了 Chelex 100、蛋白酶 K、RNase A 和微波加热。从墨西哥尤卡坦半岛的沉积物中分离出的这些细菌的 16S rDNA 基因进行 PCR 扩增,直接用于鉴定乳杆菌目细菌的种属。该方法可从 100 株分离菌中获得无酚类和蛋白质残留污染物的 gDNA。16S rDNA 扩增和测序表明,产嗜酸乳杆菌在内陆泻湖中占优势,而戊糖片球菌、植物乳杆菌、乳杆菌属和发酵乳杆菌在牲畜养殖场的土壤中最为丰富。Chelex 100-微波法中使用的 Chelex 100、酶和微波加热的组合可在不到 20 分钟的时间内从革兰氏阳性和革兰氏阴性细菌中大量产生高度纯的 gDNA。

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