Cargando…
Roles of Organohalide-Respiring Dehalococcoidia in Carbon Cycling
The class Dehalococcoidia within the Chloroflexi phylum comprises the obligate organohalide-respiring genera Dehalococcoides, Dehalogenimonas, and “Candidatus Dehalobium.” Knowledge of the unique ecophysiology and biochemistry of Dehalococcoidia has been largely derived from studies with enrichment...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7289593/ https://www.ncbi.nlm.nih.gov/pubmed/32518199 http://dx.doi.org/10.1128/mSystems.00757-19 |
_version_ | 1783545493322727424 |
---|---|
author | Yang, Yi Sanford, Robert Yan, Jun Chen, Gao Cápiro, Natalie L. Li, Xiuying Löffler, Frank E. |
author_facet | Yang, Yi Sanford, Robert Yan, Jun Chen, Gao Cápiro, Natalie L. Li, Xiuying Löffler, Frank E. |
author_sort | Yang, Yi |
collection | PubMed |
description | The class Dehalococcoidia within the Chloroflexi phylum comprises the obligate organohalide-respiring genera Dehalococcoides, Dehalogenimonas, and “Candidatus Dehalobium.” Knowledge of the unique ecophysiology and biochemistry of Dehalococcoidia has been largely derived from studies with enrichment cultures and isolates from sites impacted with chlorinated pollutants; however, culture-independent surveys found Dehalococcoidia sequences in marine, freshwater, and terrestrial biomes considered to be pristine (i.e., not impacted with organohalogens of anthropogenic origin). The broad environmental distribution of Dehalococcoidia, as well as other organohalide-respiring bacteria, supports the concept of active halogen cycling and the natural formation of organohalogens in various ecosystems. Dechlorination reduces recalcitrance and renders organics susceptible to metabolic oxidation by diverse microbial taxa. During reductive dechlorination, hydrogenotrophic organohalide-respiring bacteria, in particular Dehalococcoidia, can consume hydrogen to low consumption threshold concentrations (<0.3 nM) and enable syntrophic oxidation processes. These functional attributes and the broad distribution imply that Dehalococcoidia play relevant roles in carbon cycling in anoxic ecosystems. |
format | Online Article Text |
id | pubmed-7289593 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-72895932020-06-25 Roles of Organohalide-Respiring Dehalococcoidia in Carbon Cycling Yang, Yi Sanford, Robert Yan, Jun Chen, Gao Cápiro, Natalie L. Li, Xiuying Löffler, Frank E. mSystems Perspective The class Dehalococcoidia within the Chloroflexi phylum comprises the obligate organohalide-respiring genera Dehalococcoides, Dehalogenimonas, and “Candidatus Dehalobium.” Knowledge of the unique ecophysiology and biochemistry of Dehalococcoidia has been largely derived from studies with enrichment cultures and isolates from sites impacted with chlorinated pollutants; however, culture-independent surveys found Dehalococcoidia sequences in marine, freshwater, and terrestrial biomes considered to be pristine (i.e., not impacted with organohalogens of anthropogenic origin). The broad environmental distribution of Dehalococcoidia, as well as other organohalide-respiring bacteria, supports the concept of active halogen cycling and the natural formation of organohalogens in various ecosystems. Dechlorination reduces recalcitrance and renders organics susceptible to metabolic oxidation by diverse microbial taxa. During reductive dechlorination, hydrogenotrophic organohalide-respiring bacteria, in particular Dehalococcoidia, can consume hydrogen to low consumption threshold concentrations (<0.3 nM) and enable syntrophic oxidation processes. These functional attributes and the broad distribution imply that Dehalococcoidia play relevant roles in carbon cycling in anoxic ecosystems. American Society for Microbiology 2020-06-09 /pmc/articles/PMC7289593/ /pubmed/32518199 http://dx.doi.org/10.1128/mSystems.00757-19 Text en Copyright © 2020 Yang et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Perspective Yang, Yi Sanford, Robert Yan, Jun Chen, Gao Cápiro, Natalie L. Li, Xiuying Löffler, Frank E. Roles of Organohalide-Respiring Dehalococcoidia in Carbon Cycling |
title | Roles of Organohalide-Respiring Dehalococcoidia in Carbon Cycling |
title_full | Roles of Organohalide-Respiring Dehalococcoidia in Carbon Cycling |
title_fullStr | Roles of Organohalide-Respiring Dehalococcoidia in Carbon Cycling |
title_full_unstemmed | Roles of Organohalide-Respiring Dehalococcoidia in Carbon Cycling |
title_short | Roles of Organohalide-Respiring Dehalococcoidia in Carbon Cycling |
title_sort | roles of organohalide-respiring dehalococcoidia in carbon cycling |
topic | Perspective |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7289593/ https://www.ncbi.nlm.nih.gov/pubmed/32518199 http://dx.doi.org/10.1128/mSystems.00757-19 |
work_keys_str_mv | AT yangyi rolesoforganohaliderespiringdehalococcoidiaincarboncycling AT sanfordrobert rolesoforganohaliderespiringdehalococcoidiaincarboncycling AT yanjun rolesoforganohaliderespiringdehalococcoidiaincarboncycling AT chengao rolesoforganohaliderespiringdehalococcoidiaincarboncycling AT capironataliel rolesoforganohaliderespiringdehalococcoidiaincarboncycling AT lixiuying rolesoforganohaliderespiringdehalococcoidiaincarboncycling AT lofflerfranke rolesoforganohaliderespiringdehalococcoidiaincarboncycling |