首页> 外文期刊>Applied and Environmental Microbiology >Abundance of Dioxygenase Genes Similar to Ralstonia sp. Strain U2 nagAc Is Correlated with Naphthalene Concentrations in Coal Tar-Contaminated Freshwater Sediments
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Abundance of Dioxygenase Genes Similar to Ralstonia sp. Strain U2 nagAc Is Correlated with Naphthalene Concentrations in Coal Tar-Contaminated Freshwater Sediments

机译:类似于Ralstonia sp。的双加氧酶基因的丰度。 U2 nagAc菌株与煤焦油污染的淡水沉积物中的萘浓度相关

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We designed a real-time PCR assay able to recognize dioxygenase large-subunit gene sequences with more than 90% similarity to the Ralstonia sp. strain U2 nagAc gene (nagAc-like gene sequences) in order to study the importance of organisms carrying these genes in the biodegradation of naphthalene. Sequencing of PCR products indicated that this real-time PCR assay was specific and able to detect a variety of nagAc-like gene sequences. One to 100 ng of contaminated-sediment total DNA in 25-μl reaction mixtures produced an amplification efficiency of 0.97 without evident PCR inhibition. The assay was applied to surficial freshwater sediment samples obtained in or in close proximity to a coal tar-contaminated Superfund site. Naphthalene concentrations in the analyzed samples varied between 0.18 and 106 mg/kg of dry weight sediment. The assay for nagAc-like sequences indicated the presence of (4.1 ± 0.7) × 103 to (2.9 ± 0.3) × 105 copies of nagAc-like dioxygenase genes per μg of DNA extracted from sediment samples. These values corresponded to (1.2 ± 0.6) × 105 to (5.4 ± 0.4) × 107 copies of this target per g of dry weight sediment when losses of DNA during extraction were taken into account. There was a positive correlation between naphthalene concentrations and nagAc-like gene copies per microgram of DNA (r = 0.89) and per gram of dry weight sediment (r = 0.77). These results provide evidence of the ecological significance of organisms carrying nagAc-like genes in the biodegradation of naphthalene.
机译:我们设计了一种实时PCR分析方法,该方法能够识别与Ralstonia sp具有90%以上相似性的双加氧酶大亚基基因序列。菌株U2 nagAc基因(nagAc样基因序列),以便研究携带这些基因的生物在萘生物降解中的重要性。 PCR产物的测序表明,这种实时PCR测定具有特异性,能够检测多种nagAc样基因序列。 25μl反应混合物中1到100 ng的受污染的沉积物总DNA产生的扩增效率为0.97,而没有明显的PCR抑制作用。该测定法适用于在受煤焦油污染的超级基金地点或附近地区获得的表面淡水沉积物样本。分析样品中的萘浓度在0.18至106 mg / kg干重沉积物之间变化。对nagAc样序列的分析表明,每微克从沉积物样品中提取的DNA,存在(4.1±0.7)×103至(2.9±0.3)×105拷贝的nagAc样双加氧酶基因。当考虑到提取过程中DNA的损失时,这些值对应于每克干重沉积物的(1.2±0.6)×105至(5.4±0.4)×107拷贝的目标值。萘浓度与每微克DNA(r = 0.89)和每克干重沉积物(r = 0.77)的nagAc样基因拷贝之间呈正相关。这些结果提供了携带nagAc样基因的生物在萘的生物降解中的生态学意义的证据。

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