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Brief Bioinform. 2019 Jul 19;20(4):1151-1159. doi: 10.1093/bib/bbx105.
2
PCB dechlorination hotspots and reductive dehalogenase genes in sediments from a contaminated wastewater lagoon.受污染废水塘底泥中的 PCB 脱氯热点和还原脱卤酶基因。
Environ Sci Pollut Res Int. 2018 Jun;25(17):16376-16388. doi: 10.1007/s11356-017-9872-x. Epub 2017 Aug 12.
3
Release of Airborne Polychlorinated Biphenyls from New Bedford Harbor Results in Elevated Concentrations in the Surrounding Air.新贝德福德港释放的空气中多氯联苯导致周围空气中浓度升高。
Environ Sci Technol Lett. 2017 Apr 11;4(4):127-131. doi: 10.1021/acs.estlett.7b00047. Epub 2017 Feb 21.
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Ultra-high-throughput microbial community analysis on the Illumina HiSeq and MiSeq platforms.Illumina HiSeq 和 MiSeq 平台上的超高通量微生物群落分析。
ISME J. 2012 Aug;6(8):1621-4. doi: 10.1038/ismej.2012.8. Epub 2012 Mar 8.
5
Record of PCB congeners, sorbents and potential toxicity in core samples in Indiana Harbor and Ship Canal.印第安纳港和船运运河中 PCB 同系物、吸附剂和潜在毒性的岩芯样本记录。
Chemosphere. 2011 Oct;85(3):542-7. doi: 10.1016/j.chemosphere.2011.08.018. Epub 2011 Sep 6.
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Examining the global distribution of dominant archaeal populations in soil.研究土壤中优势古菌种群的全球分布。
ISME J. 2011 May;5(5):908-17. doi: 10.1038/ismej.2010.171. Epub 2010 Nov 18.
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The MIQE guidelines: minimum information for publication of quantitative real-time PCR experiments.MIQE指南:实时定量PCR实验发表的最低信息要求
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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.

DOI:10.1016/j.dib.2021.107546
PMID:34820490
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8601980/
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。