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一个芳烃污染场地地下水中II类芳香环羟基化双加氧酶基因丰度和种类的变化

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

作者信息

Taylor Paul M, Janssen Peter H

机构信息

Department of Microbiology and Immunology, University of Melbourne, Parkville, Victoria 3010, Australia.

出版信息

Environ Microbiol. 2005 Jan;7(1):140-6. doi: 10.1111/j.1462-2920.2004.00679.x.

Abstract

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.

摘要

采用II类芳环羟化双加氧酶(RHD)基因作为探针,通过定量DNA - DNA杂交技术,测定了澳大利亚悉尼附近一个受芳烃污染垃圾填埋场地下水中编码RHD的基因丰度。在这个异质场地的七个不同位置采集的地下水样本中,以提取的DNA为模板进行杂交,杂交信号强度存在显著差异。这被解释为表明RHD基因丰度存在变化。从每个地下水样本的DNA构建了聚合酶链反应(PCR)扩增的RHD基因片段的克隆文库。RHD基因丰度较高的样本文库中,主要是一组细菌II类RHD基因,称为S - 簇,该基因簇尚未在培养的分离物中发现。这些地下水样本中未检测到石油烃。另一组II类RHD基因序列,称为T - 簇,在从含有可检测水平的总石油烃和芳烃但RHD基因丰度较低的地下水样本中制备的RHD基因克隆文库中占主导地位。这些新基因的宿主、原位表达以及它们所编码酶的底物仍然未知。已知的芳烃降解细菌基因稀缺,而新基因在数量上占优势,这表明这些新基因的宿主可能在该场地的芳烃降解中发挥重要作用。

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