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Identification of Bacteria Utilizing Biphenyl, Benzoate, and Naphthalene in Long-Term Contaminated Soil

机译:长期污染土壤中利用联苯,苯甲酸酯和萘进行细菌鉴定

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摘要

Bacteria were identified associated with biodegradation of aromatic pollutants biphenyl, benzoate, and naphthalene in a long-term polychlorinated biphenyl- and polyaromatic hydrocarbon-contaminated soil. In order to avoid biases of culture-based approaches, stable isotope probing was applied in combination with sequence analysis of 16 S rRNA gene pyrotags amplified from 13C-enriched DNA fractions. Special attention was paid to pyrosequencing data analysis in order to eliminate the errors caused by either generation of amplicons (random errors caused by DNA polymerase, formation of chimeric sequences) or sequencing itself. Therefore, sample DNA was amplified, sequenced, and analyzed along with the DNA of a mock community constructed out of 8 bacterial strains. This warranted that appropriate tools and parameters were chosen for sequence data processing. 13C-labeled metagenomes isolated after the incubation of soil samples with all three studied aromatics were largely dominated by Proteobacteria, namely sequences clustering with the genera Rhodanobacter Burkholderia, Pandoraea, Dyella as well as some Rudaea- and Skermanella-related ones. Pseudomonads were mostly labeled by 13C from naphthalene and benzoate. The results of this study show that many biphenyl/benzoate-assimilating bacteria derive carbon also from naphthalene, pointing out broader biodegradation abilities of some soil microbiota. The results also demonstrate that, in addition to traditionally isolated genera of degradative bacteria, yet-to-be cultured bacteria are important players in bioremediation. Overall, the study contributes to our understanding of biodegradation processes in contaminated soil. At the same time our results show the importance of sequencing and analyzing a mock community in order to more correctly process and analyze sequence data.
机译:在长期被多氯联苯和多芳烃污染的土壤中,细菌与芳香族污染物联苯,苯甲酸酯和萘的生物降解有关。为了避免基于培养方法的偏倚,将稳定的同位素探测与从 13 C富集的DNA片段扩增的16 S rRNA基因焦标记的序列分析相结合。特别注意焦磷酸测序数据分析,以消除由扩增子的产生(DNA聚合酶,嵌合序列的形成引起的随机误差)或测序本身引起的错误。因此,样本DNA连同由8个细菌菌株组成的模拟群落的DNA一起被扩增,测序和分析。这保证了为序列数据处理选择了适当的工具和参数。在土壤样品中与所有三种研究的芳香族化合物一起孵育后分离出的 13 C标记的基因组主要由变形杆菌控制,即与罗丹杆菌属伯克霍尔德氏菌,潘多拉菌,狄拉氏菌以及一些鲁达氏菌和沙门氏菌属聚类的序列。相关的。假单胞菌大多由萘和苯甲酸酯中的 13 C标记。这项研究的结果表明,许多联苯/苯甲酸酯同化细菌也从萘中衍生出碳,这表明某些土壤微生物具有更广泛的生物降解能力。结果还表明,除了传统上分离的降解细菌属以外,尚待培养的细菌是生物修复的重要参与者。总的来说,这项研究有助于我们了解受污染土壤中的生物降解过程。同时,我们的结果显示了对模拟社区进行测序和分析的重要性,以便更正确地处理和分析序列数据。

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