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Vitamin and Amino Acid Auxotrophy in Anaerobic Consortia Operating under Methanogenic Conditions
Syntrophy among Archaea and Bacteria facilitates the anaerobic degradation of organic compounds to CH(4) and CO(2). Particularly during aliphatic and aromatic hydrocarbon mineralization, as in the case of crude oil reservoirs and petroleum-contaminated sediments, metabolic interactions between oblig...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Society for Microbiology
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663940/ https://www.ncbi.nlm.nih.gov/pubmed/29104938 http://dx.doi.org/10.1128/mSystems.00038-17 |
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author | Hubalek, Valerie Buck, Moritz Tan, BoonFei Foght, Julia Wendeberg, Annelie Berry, David Bertilsson, Stefan Eiler, Alexander |
author_facet | Hubalek, Valerie Buck, Moritz Tan, BoonFei Foght, Julia Wendeberg, Annelie Berry, David Bertilsson, Stefan Eiler, Alexander |
author_sort | Hubalek, Valerie |
collection | PubMed |
description | Syntrophy among Archaea and Bacteria facilitates the anaerobic degradation of organic compounds to CH(4) and CO(2). Particularly during aliphatic and aromatic hydrocarbon mineralization, as in the case of crude oil reservoirs and petroleum-contaminated sediments, metabolic interactions between obligate mutualistic microbial partners are of central importance. Using micromanipulation combined with shotgun metagenomic approaches, we describe the genomes of complex consortia within short-chain alkane-degrading cultures operating under methanogenic conditions. Metabolic reconstruction revealed that only a small fraction of genes in the metagenome-assembled genomes encode the capacity for fermentation of alkanes facilitated by energy conservation linked to H(2) metabolism. Instead, the presence of inferred lifestyles based on scavenging anabolic products and intermediate fermentation products derived from detrital biomass was a common feature. Additionally, inferred auxotrophy for vitamins and amino acids suggests that the hydrocarbon-degrading microbial assemblages are structured and maintained by multiple interactions beyond the canonical H(2)-producing and syntrophic alkane degrader-methanogen partnership. Compared to previous work, our report points to a higher order of complexity in microbial consortia engaged in anaerobic hydrocarbon transformation. IMPORTANCE Microbial interactions between Archaea and Bacteria mediate many important chemical transformations in the biosphere from degrading abundant polymers to synthesis of toxic compounds. Two of the most pressing issues in microbial interactions are how consortia are established and how we can modulate these microbial communities to express desirable functions. Here, we propose that public goods (i.e., metabolites of high energy demand in biosynthesis) facilitate energy conservation for life under energy-limited conditions and determine the assembly and function of the consortia. Our report suggests that an understanding of public good dynamics could result in new ways to improve microbial pollutant degradation in anaerobic systems. |
format | Online Article Text |
id | pubmed-5663940 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-56639402017-11-03 Vitamin and Amino Acid Auxotrophy in Anaerobic Consortia Operating under Methanogenic Conditions Hubalek, Valerie Buck, Moritz Tan, BoonFei Foght, Julia Wendeberg, Annelie Berry, David Bertilsson, Stefan Eiler, Alexander mSystems Research Article Syntrophy among Archaea and Bacteria facilitates the anaerobic degradation of organic compounds to CH(4) and CO(2). Particularly during aliphatic and aromatic hydrocarbon mineralization, as in the case of crude oil reservoirs and petroleum-contaminated sediments, metabolic interactions between obligate mutualistic microbial partners are of central importance. Using micromanipulation combined with shotgun metagenomic approaches, we describe the genomes of complex consortia within short-chain alkane-degrading cultures operating under methanogenic conditions. Metabolic reconstruction revealed that only a small fraction of genes in the metagenome-assembled genomes encode the capacity for fermentation of alkanes facilitated by energy conservation linked to H(2) metabolism. Instead, the presence of inferred lifestyles based on scavenging anabolic products and intermediate fermentation products derived from detrital biomass was a common feature. Additionally, inferred auxotrophy for vitamins and amino acids suggests that the hydrocarbon-degrading microbial assemblages are structured and maintained by multiple interactions beyond the canonical H(2)-producing and syntrophic alkane degrader-methanogen partnership. Compared to previous work, our report points to a higher order of complexity in microbial consortia engaged in anaerobic hydrocarbon transformation. IMPORTANCE Microbial interactions between Archaea and Bacteria mediate many important chemical transformations in the biosphere from degrading abundant polymers to synthesis of toxic compounds. Two of the most pressing issues in microbial interactions are how consortia are established and how we can modulate these microbial communities to express desirable functions. Here, we propose that public goods (i.e., metabolites of high energy demand in biosynthesis) facilitate energy conservation for life under energy-limited conditions and determine the assembly and function of the consortia. Our report suggests that an understanding of public good dynamics could result in new ways to improve microbial pollutant degradation in anaerobic systems. American Society for Microbiology 2017-10-31 /pmc/articles/PMC5663940/ /pubmed/29104938 http://dx.doi.org/10.1128/mSystems.00038-17 Text en Copyright © 2017 Hubalek 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 | Research Article Hubalek, Valerie Buck, Moritz Tan, BoonFei Foght, Julia Wendeberg, Annelie Berry, David Bertilsson, Stefan Eiler, Alexander Vitamin and Amino Acid Auxotrophy in Anaerobic Consortia Operating under Methanogenic Conditions |
title | Vitamin and Amino Acid Auxotrophy in Anaerobic Consortia Operating under Methanogenic Conditions |
title_full | Vitamin and Amino Acid Auxotrophy in Anaerobic Consortia Operating under Methanogenic Conditions |
title_fullStr | Vitamin and Amino Acid Auxotrophy in Anaerobic Consortia Operating under Methanogenic Conditions |
title_full_unstemmed | Vitamin and Amino Acid Auxotrophy in Anaerobic Consortia Operating under Methanogenic Conditions |
title_short | Vitamin and Amino Acid Auxotrophy in Anaerobic Consortia Operating under Methanogenic Conditions |
title_sort | vitamin and amino acid auxotrophy in anaerobic consortia operating under methanogenic conditions |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663940/ https://www.ncbi.nlm.nih.gov/pubmed/29104938 http://dx.doi.org/10.1128/mSystems.00038-17 |
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