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Microbial communities in polychlorinated biphenyl (PCB)-contaminated wastewater lagoon sediments: PCB congener, quantitative PCR, and 16S rRNA gene amplicon sequencing datasets

机译:多氯化二苯基(PCB)中的微生物群落 - 含废水泻湖沉积物:PCB同学,定量PCR和16S rRNA基因扩增的数据集

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The potential for aerobic and anaerobic microbial natural attenuation of PCBs in freshwater sediments is described by PCB congener, quantitative PCR, and 16S rRNA gene amplicon sequencing datasets generated, in duplicate, from 27 sediment samples collected from a PCB-contaminated freshwater lagoon (54 samples total). Sediment samples were subjected to a hexane PCB extraction protocol and the concentrations of 209 PCB congeners were determined in hexane extracts by gas chromatography with a tandem mass spectrometry detection. DNA was extracted from sediments sediment samples and used for qPCR and 16S rRNA amplicon sequencing. The abundance of 16S rRNA genes (i.e.,Dehalococcoidesand putative dechlorinating Chloroflexi) and functional genes (i.e., reductive dehalogenase (rdhA) and biphenyl dioxygenase (bphA)) associated with aerobic and anaerobic PCB biodegradation, along with the total 16S rRNA genes abundance, was determined by SYBR green qPCR. The microbial community composition and structure in all sediment samples was obtained by 16S rRNA gene amplicon sequencing. Primers targeting the 16S rRNA gene V4 region were used to produce 16S rRNA gene amplicons that were sequencing with the high-throughput Illumina MiSeq platform and sequencing chemistry. The 16S rRNA gene sequencing dataset along with PCB congener and qPCR datasets included as metadata, could be reused in meta-analyses that aim to determine microbial community interactions in contaminated environments, and uncover relationships between microbial community structure and environmental variable (e.g., PCB congener concentrations).
机译:淡水沉积物中PCB的有氧和厌氧微生物自然衰减的潜力由PCB同学,定量PCR和16S rRNA基因扩增子测序数据集重复于来自PCB污染的淡水泻湖收集的27个沉积物样本(54个样品全部的)。对沉积物样品进行己烷PCB萃取方案,并通过气相色谱法测定209pcb同一器的浓度,通过气相色谱法测定串联质谱检测。从沉积物沉积物样品中提取DNA,用于QPCR和16S rRNA扩增子测序。与需氧和厌氧PCB生物降解相关的16S rRNA基因(即,去卤体和推定的脱氯脱氯脱氯脱氯脱氯(即脱卤素和推定的氯化脱氯)和官能基因(即还原脱氢酶(即,厌氧PCB生物降解以及总16S rRNA基因的丰度由Sybr Green QPCR决定。所有沉积物样品中的微生物群落组成和结构是通过16S RRNA基因扩增子测序获得的。靶向16S rRNA基因V4区域的引物用于产生16S rRNA基因扩增子,其用高通量Illumina miseq平台和测序化学测序。将16S rRNA基因测序数据集与PCB同一组和QPCR数据集一起作为元数据重复使用,其旨在确定污染环境中的微生物群落相互作用,以及微生物群落结构和环境变量之间的揭示关系(例如,PCB Congener之间的关系浓度)。

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