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Variations in the abundance and identity of class II aromatic ring-hydroxylating dioxygenase genes in groundwater at an aromatic hydrocarbon-contaminated site

机译:芳香烃污染场所地下水中II类芳香环羟化双加氧酶基因的丰度和同一性变化

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摘要

The abundance of genes encoding aromatic ring-hydroxylating dioxygenases (RHDs) in the groundwater at an aromatic hydrocarbon-contaminated landfill near Sydney, Australia, was determined by quantitative DNA-DNA hybridization using class II RHD genes as probes. There were marked differences in hybridization signal intensity against DNA extracted from the groundwater at seven different locations across this heterogeneous site. This was interpreted as indicating variation in RHD gene abundance. Clone libraries of polymerase chain reaction (PCR)-amplified RHD gene fragments were constructed from DNA from each of the groundwater samples. The libraries from the samples with greater RHD gene abundance were dominated by a group of bacterial class II RHD genes, designated the S-cluster, that has yet to be found in cultured isolates. These groundwater samples contained no detectable petroleum hydrocarbons. A second group of class II RHD gene sequences, designated the T-cluster, dominated RHD gene clone libraries prepared from groundwater samples that contained detectable levels of total petroleum and aromatic hydrocarbons but lower RHD gene abundance. The hosts and in situ expression of these novel genes, and the substrates of the enzymes they encode, remain unknown. The scarcity of genes from known aromatic hydrocarbon-degrading bacteria and the numerical dominance of the novel genes suggest that the hosts of these novel genes may play an important role in aromatic hydrocarbon degradation at this site.
机译:通过使用II类RHD基因作为探针,通过定量DNA-DNA杂交测定了澳大利亚悉尼附近一个芳香烃污染的垃圾填埋场的地下水中编码芳香环羟化双加氧酶(RHD)的基因的丰度。在这个异质位点的七个不同位置,从地下水提取的DNA的杂交信号强度存在明显差异。这被解释为指示RHD基因丰度的变化。聚合酶链反应(PCR)扩增的RHD基因片段的克隆文库是从每个地下水样品的DNA中构建的。具有较高RHD基因丰度的样品中的文库由一组细菌II类RHD基因(称为S-簇)控制,该基因尚未在培养的分离物中发现。这些地下水样品不含可检测的石油烃。第二类II类RHD基因序列(称为T-簇)主导着RHD基因克隆文库,该文库是从地下水样品中制备的,该样品包含可检测的总石油和芳烃含量,但RHD基因丰度较低。这些新基因的宿主和原位表达,以及它们编码的酶的底物仍然未知。来自已知的芳烃降解细菌的基因的稀缺性和新基因的数值优势表明,这些新基因的宿主可能在该部位的芳烃降解中起重要作用。

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