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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...

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Autores principales: Hubalek, Valerie, Buck, Moritz, Tan, BoonFei, Foght, Julia, Wendeberg, Annelie, Berry, David, Bertilsson, Stefan, Eiler, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2017
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.
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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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