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Conservation of Energetic Pathways for Electroautotrophy in the Uncultivated Candidate Order Tenderiales
Electromicrobiology can be used to understand extracellular electron uptake in previously undescribed chemolithotrophs. Enrichment and characterization of the uncultivated electroautotroph “Candidatus Tenderia electrophaga” using electromicrobiology led to the designation of the order Tenderiales. R...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9599434/ https://www.ncbi.nlm.nih.gov/pubmed/36069437 http://dx.doi.org/10.1128/msphere.00223-22 |
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author | Eddie, Brian J. Bird, Lina J. Pelikan, Claus Mussmann, Marc Martínez-Pérez, Clara Pinamang, Princess Malanoski, Anthony P. Glaven, Sarah M. |
author_facet | Eddie, Brian J. Bird, Lina J. Pelikan, Claus Mussmann, Marc Martínez-Pérez, Clara Pinamang, Princess Malanoski, Anthony P. Glaven, Sarah M. |
author_sort | Eddie, Brian J. |
collection | PubMed |
description | Electromicrobiology can be used to understand extracellular electron uptake in previously undescribed chemolithotrophs. Enrichment and characterization of the uncultivated electroautotroph “Candidatus Tenderia electrophaga” using electromicrobiology led to the designation of the order Tenderiales. Representative Tenderiales metagenome-assembled genomes (MAGs) have been identified in a number of environmental surveys, yet a comprehensive characterization of conserved genes for extracellular electron uptake has thus far not been conducted. Using comparative genomics, we identified conserved orthologous genes within the Tenderiales and nearest-neighbor orders important for extracellular electron uptake based on a previously proposed pathway from “Ca. Tenderia electrophaga.” The Tenderiales contained a conserved cluster we designated uetABCDEFGHIJ, which encodes proteins containing features that would enable transport of extracellular electrons to cytoplasmic membrane-bound energy-transducing complexes such as two conserved cytochrome cbb(3) oxidases. For example, UetJ is predicted to be an extracellular undecaheme c-type cytochrome that forms a heme wire. We also identified clusters of genes predicted to facilitate assembly and maturation of electron transport proteins, as well as cellular attachment to surfaces. Autotrophy among the Tenderiales is supported by the presence of carbon fixation and stress response pathways that could allow cellular growth by extracellular electron uptake. Key differences between the Tenderiales and other known neutrophilic iron oxidizers were revealed, including very few Cyc2 genes in the Tenderiales. Our results reveal a possible conserved pathway for extracellular electron uptake and suggest that the Tenderiales have an ecological role in coupling metal or mineral redox chemistry and the carbon cycle in marine and brackish sediments. IMPORTANCE Chemolithotrophic bacteria capable of extracellular electron uptake to drive energy metabolism and CO(2) fixation are known as electroautotrophs. The recently described order Tenderiales contains the uncultivated electroautotroph “Ca. Tenderia electrophaga.” The “Ca. Tenderia electrophaga” genome contains genes proposed to make up a previously undescribed extracellular electron uptake pathway. Here, we use comparative genomics to show that this pathway is well conserved among Tenderiales spp. recovered by metagenome-assembled genomes. This conservation extends to near neighbors of the Tenderiales but not to other well-studied chemolithotrophs, including iron and sulfur oxidizers, indicating that these genes may be useful markers of growth using insoluble extracellular electron donors. Our findings suggest that extracellular electron uptake and electroautotrophy may be pervasive among the Tenderiales, and the geographic locations from which metagenome-assembled genomes were recovered offer clues to their natural ecological niche. |
format | Online Article Text |
id | pubmed-9599434 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-95994342022-10-27 Conservation of Energetic Pathways for Electroautotrophy in the Uncultivated Candidate Order Tenderiales Eddie, Brian J. Bird, Lina J. Pelikan, Claus Mussmann, Marc Martínez-Pérez, Clara Pinamang, Princess Malanoski, Anthony P. Glaven, Sarah M. mSphere Research Article Electromicrobiology can be used to understand extracellular electron uptake in previously undescribed chemolithotrophs. Enrichment and characterization of the uncultivated electroautotroph “Candidatus Tenderia electrophaga” using electromicrobiology led to the designation of the order Tenderiales. Representative Tenderiales metagenome-assembled genomes (MAGs) have been identified in a number of environmental surveys, yet a comprehensive characterization of conserved genes for extracellular electron uptake has thus far not been conducted. Using comparative genomics, we identified conserved orthologous genes within the Tenderiales and nearest-neighbor orders important for extracellular electron uptake based on a previously proposed pathway from “Ca. Tenderia electrophaga.” The Tenderiales contained a conserved cluster we designated uetABCDEFGHIJ, which encodes proteins containing features that would enable transport of extracellular electrons to cytoplasmic membrane-bound energy-transducing complexes such as two conserved cytochrome cbb(3) oxidases. For example, UetJ is predicted to be an extracellular undecaheme c-type cytochrome that forms a heme wire. We also identified clusters of genes predicted to facilitate assembly and maturation of electron transport proteins, as well as cellular attachment to surfaces. Autotrophy among the Tenderiales is supported by the presence of carbon fixation and stress response pathways that could allow cellular growth by extracellular electron uptake. Key differences between the Tenderiales and other known neutrophilic iron oxidizers were revealed, including very few Cyc2 genes in the Tenderiales. Our results reveal a possible conserved pathway for extracellular electron uptake and suggest that the Tenderiales have an ecological role in coupling metal or mineral redox chemistry and the carbon cycle in marine and brackish sediments. IMPORTANCE Chemolithotrophic bacteria capable of extracellular electron uptake to drive energy metabolism and CO(2) fixation are known as electroautotrophs. The recently described order Tenderiales contains the uncultivated electroautotroph “Ca. Tenderia electrophaga.” The “Ca. Tenderia electrophaga” genome contains genes proposed to make up a previously undescribed extracellular electron uptake pathway. Here, we use comparative genomics to show that this pathway is well conserved among Tenderiales spp. recovered by metagenome-assembled genomes. This conservation extends to near neighbors of the Tenderiales but not to other well-studied chemolithotrophs, including iron and sulfur oxidizers, indicating that these genes may be useful markers of growth using insoluble extracellular electron donors. Our findings suggest that extracellular electron uptake and electroautotrophy may be pervasive among the Tenderiales, and the geographic locations from which metagenome-assembled genomes were recovered offer clues to their natural ecological niche. American Society for Microbiology 2022-09-07 /pmc/articles/PMC9599434/ /pubmed/36069437 http://dx.doi.org/10.1128/msphere.00223-22 Text en https://doi.org/10.1128/AuthorWarrantyLicense.v1This is a work of the U.S. Government and is not subject to copyright protection in the United States. Foreign copyrights may apply. |
spellingShingle | Research Article Eddie, Brian J. Bird, Lina J. Pelikan, Claus Mussmann, Marc Martínez-Pérez, Clara Pinamang, Princess Malanoski, Anthony P. Glaven, Sarah M. Conservation of Energetic Pathways for Electroautotrophy in the Uncultivated Candidate Order Tenderiales |
title | Conservation of Energetic Pathways for Electroautotrophy in the Uncultivated Candidate Order Tenderiales |
title_full | Conservation of Energetic Pathways for Electroautotrophy in the Uncultivated Candidate Order Tenderiales |
title_fullStr | Conservation of Energetic Pathways for Electroautotrophy in the Uncultivated Candidate Order Tenderiales |
title_full_unstemmed | Conservation of Energetic Pathways for Electroautotrophy in the Uncultivated Candidate Order Tenderiales |
title_short | Conservation of Energetic Pathways for Electroautotrophy in the Uncultivated Candidate Order Tenderiales |
title_sort | conservation of energetic pathways for electroautotrophy in the uncultivated candidate order tenderiales |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9599434/ https://www.ncbi.nlm.nih.gov/pubmed/36069437 http://dx.doi.org/10.1128/msphere.00223-22 |
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