Cargando…
Potential for microbial H(2) and metal transformations associated with novel bacteria and archaea in deep terrestrial subsurface sediments
Geological sequestration in deep underground repositories is the prevailing proposed route for radioactive waste disposal. After the disposal of radioactive waste in the subsurface, H(2) may be produced by corrosion of steel and, ultimately, radionuclides will be exposed to the surrounding environme...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5520028/ https://www.ncbi.nlm.nih.gov/pubmed/28350393 http://dx.doi.org/10.1038/ismej.2017.39 |
_version_ | 1783251744181977088 |
---|---|
author | Hernsdorf, Alex W Amano, Yuki Miyakawa, Kazuya Ise, Kotaro Suzuki, Yohey Anantharaman, Karthik Probst, Alexander Burstein, David Thomas, Brian C Banfield, Jillian F |
author_facet | Hernsdorf, Alex W Amano, Yuki Miyakawa, Kazuya Ise, Kotaro Suzuki, Yohey Anantharaman, Karthik Probst, Alexander Burstein, David Thomas, Brian C Banfield, Jillian F |
author_sort | Hernsdorf, Alex W |
collection | PubMed |
description | Geological sequestration in deep underground repositories is the prevailing proposed route for radioactive waste disposal. After the disposal of radioactive waste in the subsurface, H(2) may be produced by corrosion of steel and, ultimately, radionuclides will be exposed to the surrounding environment. To evaluate the potential for microbial activities to impact disposal systems, we explored the microbial community structure and metabolic functions of a sediment-hosted ecosystem at the Horonobe Underground Research Laboratory, Hokkaido, Japan. Overall, we found that the ecosystem hosted organisms from diverse lineages, including many from the phyla that lack isolated representatives. The majority of organisms can metabolize H(2), often via oxidative [NiFe] hydrogenases or electron-bifurcating [FeFe] hydrogenases that enable ferredoxin-based pathways, including the ion motive Rnf complex. Many organisms implicated in H(2) metabolism are also predicted to catalyze carbon, nitrogen, iron and sulfur transformations. Notably, iron-based metabolism is predicted in a novel lineage of Actinobacteria and in a putative methane-oxidizing ANME-2d archaeon. We infer an ecological model that links microorganisms to sediment-derived resources and predict potential impacts of microbial activity on H(2) consumption and retardation of radionuclide migration. |
format | Online Article Text |
id | pubmed-5520028 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-55200282017-08-24 Potential for microbial H(2) and metal transformations associated with novel bacteria and archaea in deep terrestrial subsurface sediments Hernsdorf, Alex W Amano, Yuki Miyakawa, Kazuya Ise, Kotaro Suzuki, Yohey Anantharaman, Karthik Probst, Alexander Burstein, David Thomas, Brian C Banfield, Jillian F ISME J Original Article Geological sequestration in deep underground repositories is the prevailing proposed route for radioactive waste disposal. After the disposal of radioactive waste in the subsurface, H(2) may be produced by corrosion of steel and, ultimately, radionuclides will be exposed to the surrounding environment. To evaluate the potential for microbial activities to impact disposal systems, we explored the microbial community structure and metabolic functions of a sediment-hosted ecosystem at the Horonobe Underground Research Laboratory, Hokkaido, Japan. Overall, we found that the ecosystem hosted organisms from diverse lineages, including many from the phyla that lack isolated representatives. The majority of organisms can metabolize H(2), often via oxidative [NiFe] hydrogenases or electron-bifurcating [FeFe] hydrogenases that enable ferredoxin-based pathways, including the ion motive Rnf complex. Many organisms implicated in H(2) metabolism are also predicted to catalyze carbon, nitrogen, iron and sulfur transformations. Notably, iron-based metabolism is predicted in a novel lineage of Actinobacteria and in a putative methane-oxidizing ANME-2d archaeon. We infer an ecological model that links microorganisms to sediment-derived resources and predict potential impacts of microbial activity on H(2) consumption and retardation of radionuclide migration. Nature Publishing Group 2017-08 2017-03-28 /pmc/articles/PMC5520028/ /pubmed/28350393 http://dx.doi.org/10.1038/ismej.2017.39 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Original Article Hernsdorf, Alex W Amano, Yuki Miyakawa, Kazuya Ise, Kotaro Suzuki, Yohey Anantharaman, Karthik Probst, Alexander Burstein, David Thomas, Brian C Banfield, Jillian F Potential for microbial H(2) and metal transformations associated with novel bacteria and archaea in deep terrestrial subsurface sediments |
title | Potential for microbial H(2) and metal transformations associated with novel bacteria and archaea in deep terrestrial subsurface sediments |
title_full | Potential for microbial H(2) and metal transformations associated with novel bacteria and archaea in deep terrestrial subsurface sediments |
title_fullStr | Potential for microbial H(2) and metal transformations associated with novel bacteria and archaea in deep terrestrial subsurface sediments |
title_full_unstemmed | Potential for microbial H(2) and metal transformations associated with novel bacteria and archaea in deep terrestrial subsurface sediments |
title_short | Potential for microbial H(2) and metal transformations associated with novel bacteria and archaea in deep terrestrial subsurface sediments |
title_sort | potential for microbial h(2) and metal transformations associated with novel bacteria and archaea in deep terrestrial subsurface sediments |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5520028/ https://www.ncbi.nlm.nih.gov/pubmed/28350393 http://dx.doi.org/10.1038/ismej.2017.39 |
work_keys_str_mv | AT hernsdorfalexw potentialformicrobialh2andmetaltransformationsassociatedwithnovelbacteriaandarchaeaindeepterrestrialsubsurfacesediments AT amanoyuki potentialformicrobialh2andmetaltransformationsassociatedwithnovelbacteriaandarchaeaindeepterrestrialsubsurfacesediments AT miyakawakazuya potentialformicrobialh2andmetaltransformationsassociatedwithnovelbacteriaandarchaeaindeepterrestrialsubsurfacesediments AT isekotaro potentialformicrobialh2andmetaltransformationsassociatedwithnovelbacteriaandarchaeaindeepterrestrialsubsurfacesediments AT suzukiyohey potentialformicrobialh2andmetaltransformationsassociatedwithnovelbacteriaandarchaeaindeepterrestrialsubsurfacesediments AT anantharamankarthik potentialformicrobialh2andmetaltransformationsassociatedwithnovelbacteriaandarchaeaindeepterrestrialsubsurfacesediments AT probstalexander potentialformicrobialh2andmetaltransformationsassociatedwithnovelbacteriaandarchaeaindeepterrestrialsubsurfacesediments AT bursteindavid potentialformicrobialh2andmetaltransformationsassociatedwithnovelbacteriaandarchaeaindeepterrestrialsubsurfacesediments AT thomasbrianc potentialformicrobialh2andmetaltransformationsassociatedwithnovelbacteriaandarchaeaindeepterrestrialsubsurfacesediments AT banfieldjillianf potentialformicrobialh2andmetaltransformationsassociatedwithnovelbacteriaandarchaeaindeepterrestrialsubsurfacesediments |