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多氯联苯(PCB)污染的废水泻湖沉积物中的微生物群落:多氯联苯同系物、定量PCR和16S rRNA基因扩增子测序数据集

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

作者信息

Mattes Timothy E, Ewald Jessica M, Liang Yi, Martinez Andres, Awad Andrew M, Hornbuckle Keri C, Schnoor Jerald L

机构信息

Department of Civil and Environmental Engineering, University of Iowa, 4105 Seamans Center, Iowa City, IA 52242, USA.

Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou, China.

出版信息

Data Brief. 2021 Nov 6;39:107546. doi: 10.1016/j.dib.2021.107546. eCollection 2021 Dec.

Abstract

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., and putative dechlorinating Chloroflexi) and functional genes (i.e., reductive dehalogenase () and biphenyl dioxygenase ()) 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).

摘要

通过多氯联苯同系物、定量聚合酶链反应(qPCR)以及16S核糖体RNA(rRNA)基因扩增子测序数据集,描述了淡水沉积物中多氯联苯(PCBs)的好氧和厌氧微生物自然衰减潜力。这些数据集是对从一个受多氯联苯污染的淡水泻湖采集的27个沉积物样本(共54个样本)进行一式两份检测而生成的。沉积物样本采用己烷提取多氯联苯的方案,并通过气相色谱 - 串联质谱检测法测定己烷提取物中209种多氯联苯同系物的浓度。从沉积物样本中提取DNA,并用于qPCR和16S rRNA扩增子测序。通过SYBR绿色荧光定量PCR法测定与多氯联苯好氧和厌氧生物降解相关的16S rRNA基因(即 以及假定的脱氯绿弯菌属)和功能基因(即还原脱卤酶( )和联苯双加氧酶( ))的丰度,以及16S rRNA基因的总丰度。通过16S rRNA基因扩增子测序获得所有沉积物样本中的微生物群落组成和结构。使用靶向16S rRNA基因V4区域的引物生成16S rRNA基因扩增子,然后利用高通量Illumina MiSeq平台和测序化学方法进行测序。16S rRNA基因测序数据集以及作为元数据包含的多氯联苯同系物和qPCR数据集,可在旨在确定受污染环境中微生物群落相互作用以及揭示微生物群落结构与环境变量(如多氯联苯同系物浓度)之间关系的荟萃分析中重复使用。

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