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首页> 外文期刊>Canadian journal of microbiology >Determination of low bacterial concentrations in hyperarid Atacama soils: comparison of biochemical and microscopy methods with real-time quantitative PCR.
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Determination of low bacterial concentrations in hyperarid Atacama soils: comparison of biochemical and microscopy methods with real-time quantitative PCR.

机译:确定超干旱阿塔卡马土壤中的低细菌浓度:生化和显微镜方法与实时定量PCR的比较。

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摘要

Hyperarid Atacama soils are reported to contain significantly reduced numbers of microbes per gram of soil relative to soils from other environments. Molecular methods have been used to evaluate microbial populations in hyperarid Atacama soils; however, conflicting results across the various studies, possibly caused by this low number of microorganisms and consequent biomass, suggest that knowledge of expected DNA concentrations in these soils becomes important to interpreting data from any method regarding microbial concentrations and diversity. In this paper we compare the number of bacteria per gram of Atacama Desert soils determined by real-time quantitative polymerase chain reaction with the number of bacteria estimated by the standard methods of phospholipids fatty acid analysis, adenine composition (determined by liquid chromatography - time-of-flight mass spectrometry), and SYBR-green microscopy. The number determined by real-time quantitative polymerase chain reaction as implemented in this study was several orders of magnitude lower than that determined by the other three methods and probably underestimates the concentrations of soil bacteria, most likely because of soil binding during the DNA extraction methods. However, the other methods very possibly overestimate the bacteria concentrations owing to desiccated, intact organisms, which would stain positive in microscopy and preserve both adenine and phospholipid fatty acid for the other methods.
机译:据报道,与其他环境中的土壤相比,阿塔卡马州超高产土壤每克土壤中微生物的数量大大减少。分子方法已被用于评估高干旱阿塔卡马土壤中的微生物种群。但是,各种研究的相互矛盾的结果可能是由于微生物数量少和随之产生的生物量少引起的,这表明了解这些土壤中预期的DNA浓度对于解释任何有关微生物浓度和多样性的方法的数据变得很重要。在本文中,我们将通过实时定量聚合酶链反应测定的每克阿塔卡马沙漠土壤细菌数量与通过磷脂脂肪酸分析,腺嘌呤组成的标准方法估算的细菌数量进行比较(通过液相色谱法-时间-飞行质谱)和SYBR-Green显微镜。本研究中通过实时定量聚合酶链反应确定的数量比其他三种方法确定的数量低几个数量级,并且可能低估了土壤细菌的浓度,这很可能是由于DNA提取方法中的土壤结合。但是,其他方法很可能会由于干燥的完整生物体而高估细菌浓度,而这些微生物在显微镜下会染色呈阳性,并为其他方法保留腺嘌呤和磷脂脂肪酸。

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