Cargando…
Metabolic diversity and ecological niches of Achromatium populations revealed with single-cell genomic sequencing
Large, sulfur-cycling, calcite-precipitating bacteria in the genus Achromatium represent a significant proportion of bacterial communities near sediment-water interfaces at sites throughout the world. Our understanding of their potentially crucial roles in calcium, carbon, sulfur, nitrogen, and iron...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4530308/ https://www.ncbi.nlm.nih.gov/pubmed/26322031 http://dx.doi.org/10.3389/fmicb.2015.00822 |
_version_ | 1782384894379294720 |
---|---|
author | Mansor, Muammar Hamilton, Trinity L. Fantle, Matthew S. Macalady, Jennifer L. |
author_facet | Mansor, Muammar Hamilton, Trinity L. Fantle, Matthew S. Macalady, Jennifer L. |
author_sort | Mansor, Muammar |
collection | PubMed |
description | Large, sulfur-cycling, calcite-precipitating bacteria in the genus Achromatium represent a significant proportion of bacterial communities near sediment-water interfaces at sites throughout the world. Our understanding of their potentially crucial roles in calcium, carbon, sulfur, nitrogen, and iron cycling is limited because they have not been cultured or sequenced using environmental genomics approaches to date. We utilized single-cell genomic sequencing to obtain one incomplete and two nearly complete draft genomes for Achromatium collected at Warm Mineral Springs (WMS), FL. Based on 16S rRNA gene sequences, the three cells represent distinct and relatively distant Achromatium populations (91–92% identity). The draft genomes encode key genes involved in sulfur and hydrogen oxidation; oxygen, nitrogen and polysulfide respiration; carbon and nitrogen fixation; organic carbon assimilation and storage; chemotaxis; twitching motility; antibiotic resistance; and membrane transport. Known genes for iron and manganese energy metabolism were not detected. The presence of pyrophosphatase and vacuolar (V)-type ATPases, which are generally rare in bacterial genomes, suggests a role for these enzymes in calcium transport, proton pumping, and/or energy generation in the membranes of calcite-containing inclusions. |
format | Online Article Text |
id | pubmed-4530308 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-45303082015-08-28 Metabolic diversity and ecological niches of Achromatium populations revealed with single-cell genomic sequencing Mansor, Muammar Hamilton, Trinity L. Fantle, Matthew S. Macalady, Jennifer L. Front Microbiol Microbiology Large, sulfur-cycling, calcite-precipitating bacteria in the genus Achromatium represent a significant proportion of bacterial communities near sediment-water interfaces at sites throughout the world. Our understanding of their potentially crucial roles in calcium, carbon, sulfur, nitrogen, and iron cycling is limited because they have not been cultured or sequenced using environmental genomics approaches to date. We utilized single-cell genomic sequencing to obtain one incomplete and two nearly complete draft genomes for Achromatium collected at Warm Mineral Springs (WMS), FL. Based on 16S rRNA gene sequences, the three cells represent distinct and relatively distant Achromatium populations (91–92% identity). The draft genomes encode key genes involved in sulfur and hydrogen oxidation; oxygen, nitrogen and polysulfide respiration; carbon and nitrogen fixation; organic carbon assimilation and storage; chemotaxis; twitching motility; antibiotic resistance; and membrane transport. Known genes for iron and manganese energy metabolism were not detected. The presence of pyrophosphatase and vacuolar (V)-type ATPases, which are generally rare in bacterial genomes, suggests a role for these enzymes in calcium transport, proton pumping, and/or energy generation in the membranes of calcite-containing inclusions. Frontiers Media S.A. 2015-08-10 /pmc/articles/PMC4530308/ /pubmed/26322031 http://dx.doi.org/10.3389/fmicb.2015.00822 Text en Copyright © 2015 Mansor, Hamilton, Fantle and Macalady. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Mansor, Muammar Hamilton, Trinity L. Fantle, Matthew S. Macalady, Jennifer L. Metabolic diversity and ecological niches of Achromatium populations revealed with single-cell genomic sequencing |
title | Metabolic diversity and ecological niches of Achromatium populations revealed with single-cell genomic sequencing |
title_full | Metabolic diversity and ecological niches of Achromatium populations revealed with single-cell genomic sequencing |
title_fullStr | Metabolic diversity and ecological niches of Achromatium populations revealed with single-cell genomic sequencing |
title_full_unstemmed | Metabolic diversity and ecological niches of Achromatium populations revealed with single-cell genomic sequencing |
title_short | Metabolic diversity and ecological niches of Achromatium populations revealed with single-cell genomic sequencing |
title_sort | metabolic diversity and ecological niches of achromatium populations revealed with single-cell genomic sequencing |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4530308/ https://www.ncbi.nlm.nih.gov/pubmed/26322031 http://dx.doi.org/10.3389/fmicb.2015.00822 |
work_keys_str_mv | AT mansormuammar metabolicdiversityandecologicalnichesofachromatiumpopulationsrevealedwithsinglecellgenomicsequencing AT hamiltontrinityl metabolicdiversityandecologicalnichesofachromatiumpopulationsrevealedwithsinglecellgenomicsequencing AT fantlematthews metabolicdiversityandecologicalnichesofachromatiumpopulationsrevealedwithsinglecellgenomicsequencing AT macaladyjenniferl metabolicdiversityandecologicalnichesofachromatiumpopulationsrevealedwithsinglecellgenomicsequencing |