Study of Soil Microbiological Properties

H. Kheyrodin
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Abstract

Two strategies have been developed to improve DNA recovery in terms of yield, purity and unbiased representation of the microbial diversity. However, amplification of DNA from soil is often inhibited by co-purified contaminants. Furthermore, DNA is also suitable for PCR amplification using various DNA targets. This review presents an overview of the available methods to achieve this challenging objective. DNA was extracted from 100 g of soil using direct lysis with glass beads and SDS followed by potassium acetate precipitation, polyethylene glycol precipitation, phenol extraction and isopropanol precipitation.
土壤微生物特性研究
已经开发了两种策略来提高DNA回收率,即产量、纯度和微生物多样性的无偏表示。然而,从土壤中扩增DNA通常受到共纯化污染物的抑制。此外,DNA也适用于使用各种DNA靶标的PCR扩增。本综述概述了实现这一具有挑战性目标的可用方法。使用玻璃珠和SDS的直接裂解从100g土壤中提取DNA,然后进行乙酸钾沉淀、聚乙二醇沉淀、苯酚提取和异丙醇沉淀。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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