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Arsenic mobilization in a high arsenic groundwater revealed by metagenomic and Geochip analyses

Microbial metabolisms of arsenic, iron, sulfur, nitrogen and organic matter play important roles in arsenic mobilization in aquifer. In this study, microbial community composition and functional potentials in a high arsenic groundwater were investigated using integrated techniques of RNA- and DNA-ba...

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Autores principales: Jiang, Zhou, Li, Ping, Wang, Yanhong, Liu, Han, Wei, Dazhun, Yuan, Changguo, Wang, Helin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6736849/
https://www.ncbi.nlm.nih.gov/pubmed/31506464
http://dx.doi.org/10.1038/s41598-019-49365-w
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author Jiang, Zhou
Li, Ping
Wang, Yanhong
Liu, Han
Wei, Dazhun
Yuan, Changguo
Wang, Helin
author_facet Jiang, Zhou
Li, Ping
Wang, Yanhong
Liu, Han
Wei, Dazhun
Yuan, Changguo
Wang, Helin
author_sort Jiang, Zhou
collection PubMed
description Microbial metabolisms of arsenic, iron, sulfur, nitrogen and organic matter play important roles in arsenic mobilization in aquifer. In this study, microbial community composition and functional potentials in a high arsenic groundwater were investigated using integrated techniques of RNA- and DNA-based 16S rRNA gene sequencing, metagenomic sequencing and functional gene arrays. 16S rRNA gene sequencing showed the sample was dominated by members of Proteobacteria (62.3–75.2%), such as genera of Simplicispira (5.7–6.7%), Pseudomonas (3.3–5.7%), Ferribacterium (1.6–4.4%), Solimonas (1.8–3.2%), Geobacter (0.8–2.2%) and Sediminibacterium (0.6–2.4%). Functional potential analyses indicated that organics degradation, assimilatory sulfate reduction, As-resistant pathway, iron reduction, ammonification, nitrogen fixation, denitrification and dissimilatory nitrate reduction to ammonia were prevalent. The composition and function of microbial community and reconstructed genome bins suggest that high level of arsenite in the groundwater may be attributed to arsenate release from iron oxides reductive dissolution by the iron-reducing bacteria, and subsequent arsenate reduction by ammonia-producing bacteria featuring ars operon. This study highlights the relationship between biogeochemical cycling of arsenic and nitrogen in groundwater, which potentially occur in other aquifers with high levels of ammonia and arsenic.
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spelling pubmed-67368492019-09-20 Arsenic mobilization in a high arsenic groundwater revealed by metagenomic and Geochip analyses Jiang, Zhou Li, Ping Wang, Yanhong Liu, Han Wei, Dazhun Yuan, Changguo Wang, Helin Sci Rep Article Microbial metabolisms of arsenic, iron, sulfur, nitrogen and organic matter play important roles in arsenic mobilization in aquifer. In this study, microbial community composition and functional potentials in a high arsenic groundwater were investigated using integrated techniques of RNA- and DNA-based 16S rRNA gene sequencing, metagenomic sequencing and functional gene arrays. 16S rRNA gene sequencing showed the sample was dominated by members of Proteobacteria (62.3–75.2%), such as genera of Simplicispira (5.7–6.7%), Pseudomonas (3.3–5.7%), Ferribacterium (1.6–4.4%), Solimonas (1.8–3.2%), Geobacter (0.8–2.2%) and Sediminibacterium (0.6–2.4%). Functional potential analyses indicated that organics degradation, assimilatory sulfate reduction, As-resistant pathway, iron reduction, ammonification, nitrogen fixation, denitrification and dissimilatory nitrate reduction to ammonia were prevalent. The composition and function of microbial community and reconstructed genome bins suggest that high level of arsenite in the groundwater may be attributed to arsenate release from iron oxides reductive dissolution by the iron-reducing bacteria, and subsequent arsenate reduction by ammonia-producing bacteria featuring ars operon. This study highlights the relationship between biogeochemical cycling of arsenic and nitrogen in groundwater, which potentially occur in other aquifers with high levels of ammonia and arsenic. Nature Publishing Group UK 2019-09-10 /pmc/articles/PMC6736849/ /pubmed/31506464 http://dx.doi.org/10.1038/s41598-019-49365-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Jiang, Zhou
Li, Ping
Wang, Yanhong
Liu, Han
Wei, Dazhun
Yuan, Changguo
Wang, Helin
Arsenic mobilization in a high arsenic groundwater revealed by metagenomic and Geochip analyses
title Arsenic mobilization in a high arsenic groundwater revealed by metagenomic and Geochip analyses
title_full Arsenic mobilization in a high arsenic groundwater revealed by metagenomic and Geochip analyses
title_fullStr Arsenic mobilization in a high arsenic groundwater revealed by metagenomic and Geochip analyses
title_full_unstemmed Arsenic mobilization in a high arsenic groundwater revealed by metagenomic and Geochip analyses
title_short Arsenic mobilization in a high arsenic groundwater revealed by metagenomic and Geochip analyses
title_sort arsenic mobilization in a high arsenic groundwater revealed by metagenomic and geochip analyses
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6736849/
https://www.ncbi.nlm.nih.gov/pubmed/31506464
http://dx.doi.org/10.1038/s41598-019-49365-w
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