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首页> 外文期刊>Journal of molecular catalysis, B. Enzymatic >Ligninolytic enzymes improve soil DNA purity: Solution to methodological challenges of soil metagenomics
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Ligninolytic enzymes improve soil DNA purity: Solution to methodological challenges of soil metagenomics

机译:木质素分解酶改善土壤DNA纯度:解决土壤宏基因组学方法挑战的方法

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摘要

A new, improved and cost effective protocol for extraction of pure, high molecular weight metagenomic DNA from soil samples using ligninolytic enzymes has been developed. DNA yield of 17 μgg~(-1) of soil from termite nest soil and 25 μgg~(-1) from forest soil and size of 15-20 kb was achieved by the optimized protocol. More than 90% of DNA was recovered after purification and there was 81% reduction in humic acid content. The strategy allowed processing of several samples at a given time and yielded purified DNA. The isolated metagenomic DNA sample could be readily processed for restriction digestion and PCR amplification. The quantitative PCR revealed CP value of 21 for the treated samples whereas the untreated samples could not cross the threshold fluorescence even after 45 cycles. This clearly indicated that the isolated metagenomic DNA is amenable for molecular manipulations.
机译:已经开发了一种新的,改进的和具有成本效益的方案,该方案使用木质素分解酶从土壤样品中提取纯的,高分子量的宏基因组DNA。通过优化的方案,白蚁巢土壤的DNA产量为17μgg〜(-1),森林土壤的DNA产量为25μgg〜(-1),大小为15-20 kb。纯化后回收了超过90%的DNA,腐殖酸含量降低了81%。该策略允许在给定的时间处理几个样品,并产生纯化的DNA。分离的宏基因组DNA样品可轻松进行限制性酶切和PCR扩增。定量PCR显示,处理后的样品的CP值为21,而未经处理的样品即使经过45个循环也无法超过阈值荧光。这清楚地表明分离的宏基因组DNA适合于分子操作。

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