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Sensitive and substrate-specific detection of metabolically active microorganisms in natural microbial consortia using community isotope arrays

机译:使用社区同位素阵列对天然微生物群落中代谢活性微生物进行灵敏的底物特异性检测

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The goal of this study was to develop and validate a novel fosmid-clone-based metagenome isotope array approach - termed the community isotope array (CIArray) - for sensitive detection and identification of microorganisms assimilating a radiolabeled substrate within complex microbial communities. More specifically, a sample-specific CIArray was used to identify anoxic phenol-degrading microorganisms in activated sludge treating synthetic coke-oven wastewater in a single-sludge predenitrification-nitrification process. Hybridization of the CIArray with DNA from the ~(14)C-phenol-amended sample indicated that bacteria assimilating ~(14)C-atoms, presumably directly from phenol, under nitrate-reducing conditions were abundant in the reactor, and taxonomic assignment of the fosmid clone end sequences suggested that they belonged to the Gammaproteobacteria. The specificity of the CIArray was validated by quantification of fosmid-clone-specific DNA in density-resolved DNA fractions from samples incubated with ~(13)C-phenol, which verified that all CIArray-positive probes stemmed from microorganisms that assimilated isotopically labeled carbon. This also demonstrated that the CIArray was more sensitive than DNA-SIP, as the former enabled positive detection at a phenol concentration that failed to yield a 'heavy' DNA fraction. Finally, two operational taxonomic units distantly related to marine Gammaproteobacteria were identified to account for more than half of 16S rRNA gene clones in the 'heavy' DNA library, corroborating the CIArray-based identification.
机译:这项研究的目的是开发和验证一种新型的基于化石克隆的基于基因组的基因组同位素阵列方法-称为社区同位素阵列(CIArray)-用于敏感检测和鉴定与复杂微生物群落中的放射性标记底物相似的微生物。更具体地说,使用特定于样品的CIArray来鉴定单污泥预硝化-硝化过程中处理合成焦炉废水的活性污泥中的降解酚类的微生物。 CIArray与来自〜(14)C-苯酚修饰样品的DNA杂交表明,在硝酸盐还原条件下,可能直接来自苯酚的〜(14)C-原子同化细菌在反应器中大量存在,并且分类学分配fosmid克隆的末端序列表明它们属于γ-变形细菌。通过对〜(13)C-苯酚孵育的样品中密度分辨的DNA片段中的fosmid克隆特异性DNA进行定量,验证了CIArray的特异性,这证明了所有CIArray阳性探针均源自同化同位素标记碳的微生物。这也证明CIArray比DNA-SIP更为灵敏,因为前者可以在苯酚浓度下进行阳性检测而无法产生“重” DNA分数。最后,鉴定了两个与海洋伽玛变形杆菌远距离相关的操作分类单位,以解释“重型” DNA文库中16S rRNA基因克隆的一半以上,证实了基于CIArray的鉴定。

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