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A new method to extract and purify DNA from allophanic soils and paleosols, and potential for paleoenvironmental reconstruction and other applications

机译:从同种异体土壤和古土壤中提取和纯化DNA的新方法,及其在古环境重建和其他应用中的潜力

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摘要

Andisols, developed from late-Quaternary tephra (volcanic ash) deposits and dominated by the nanocrystalline aluminosilicate, allophane, contain large stores of organic matter and are potential reservoirs for DNA. However, DNA recovery from Andisols and other allophane-bearing soils has been difficult and inefficient because of strong chemical bonding between DNA and both allophane and organic matter, and also because much DNA can be encased and physically protected in nanopores in allophane nano/microaggregates. We have therefore developed a new two-step DNA isolation method for allophanic soils and buried paleosols, including those low in clay, which circumvents these problems. The method centres on (1) releasing mainly microbial DNA, and extracellular (unbound) DNA, using an alkaline phosphate buffer (“Rai’s lysis buffer”) that blocks re-adsorption sites on the allophanic materials, and (2) the novel application of acidified ammonium oxalate (Tamm’s reagent) to dissolve the allophane and to release DNA which had been chemically-bound and also which had been protected within nanopores. Ammonium oxalate has not previously been applied to soil DNA extraction. DNA yields up to 44.5 µg g-1 soil (oven-dry basis) were obtained from three field-moist natural allophanic soil samples from northern New Zealand using this two-step method. Following extraction, we evaluated different DNA purification methods. Gel electrophoresis of the extracted DNA followed by gel purification of the DNA from the agarose gel, despite some DNA loss, was the only purification method that removed sufficient humic material for successful DNA amplification using the polymerase chain reaction (PCR) of multiple gene regions. Sequencing of PCR products obtained from a buried allophanic paleosol at 2.2-m depth on a sandy Holocene tephra yielded endemic and exotic plants that differed from the European grasses growing currently on the soil’s surface. This difference suggests that the DNA extraction method is able to access (paleo)environmental DNA derived from previous vegetation cover. Our DNA extraction and purification method hence may be applied to Andisols and allophane-bearing paleosols, potentially offering a means to isolate paleoenvironmental DNA and thus facilitate reconstruction of past environments in volcanic landscapes, datable using tephrochronology, and also aid biodiversity understanding of andic soils and paleosols.
机译:由晚第四纪特非拉(火山灰)矿床开发而成的山iso醇,以纳米晶硅铝酸盐(铝硅铝)为主,含有大量有机物,是DNA的潜在储藏库。然而,由于DNA与Allophane和有机物之间的牢固化学键合,以及因为许多DNA可以被包裹并被物理保护在Allophane纳米/微团聚体的纳米孔中,因此从Andisols和其他带有Allophane的土壤中回收DNA一直很困难且效率低下。因此,我们开发了一种新的两步法DNA分离方法,用于解决同素异形土壤和埋藏的古土壤,包括粘土含量低的古土壤,从而避免了这些问题。该方法的重点是(1)使用碱性磷酸盐缓冲液(“ Rai's裂解缓冲液”)释放主要释放微生物DNA和细胞外(未结合的)DNA,该缓冲液会阻止同色材料上的再吸附位点,以及(2)新型应用酸化草酸铵(Tamm's试剂)以溶解玻璃纸并释放已化学结合且也已在纳米孔中保护的DNA。草酸铵以前尚未用于土壤DNA提取。使用这种两步法,从三个来自新西兰北部的田间湿润的天然异源土壤样品中获得的DNA产量高达44.5 µg g-1(以烤箱为基础)。提取后,我们评估了不同的DNA纯化方法。尽管有一些DNA缺失,但对提取的DNA进行凝胶电泳,然后再从琼脂糖凝胶中进行DNA凝胶纯化,是唯一使用多种基因区域的聚合酶链反应(PCR)去除足够的腐殖质以成功进行DNA扩增的纯化方法。对从全新世特菲拉沙丘上2.2 m深度的埋入同素异质古土壤中获得的PCR产物进行测序后,得到的特有植物和外来植物与目前在土壤表面生长的欧洲草不同。这种差异表明,DNA提取方法能够访问源自先前植被覆盖的(古)环境DNA。因此,我们的DNA提取和纯化方法可能适用于安索尔和含石蒜的古土壤,潜在地提供了一种分离古环境DNA的方法,从而促进了火山景观中过去环境的重建,利用年代学对数据进行了数据库化,并且还有助于生物多样性对Andic土壤和土壤的了解。古土壤。

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