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Biofilm growth mode promotes maximum carrying capacity and community stability during product inhibition syntrophy

Sulfate-reducing bacteria (SRB) can interact syntrophically with other community members in the absence of sulfate, and interactions with hydrogen-consuming methanogens are beneficial when these archaea consume potentially inhibitory H(2) produced by the SRB. A dual continuous culture approach was u...

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Autores principales: Brileya, Kristen A., Camilleri, Laura B., Zane, Grant M., Wall, Judy D., Fields, Matthew W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4266047/
https://www.ncbi.nlm.nih.gov/pubmed/25566209
http://dx.doi.org/10.3389/fmicb.2014.00693
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author Brileya, Kristen A.
Camilleri, Laura B.
Zane, Grant M.
Wall, Judy D.
Fields, Matthew W.
author_facet Brileya, Kristen A.
Camilleri, Laura B.
Zane, Grant M.
Wall, Judy D.
Fields, Matthew W.
author_sort Brileya, Kristen A.
collection PubMed
description Sulfate-reducing bacteria (SRB) can interact syntrophically with other community members in the absence of sulfate, and interactions with hydrogen-consuming methanogens are beneficial when these archaea consume potentially inhibitory H(2) produced by the SRB. A dual continuous culture approach was used to characterize population structure within a syntrophic biofilm formed by the SRB Desulfovibrio vulgaris Hildenborough and the methanogenic archaeum Methanococcus maripaludis. Under the tested conditions, monocultures of D. vulgaris formed thin, stable biofilms, but monoculture M. maripaludis did not. Microscopy of intact syntrophic biofilm confirmed that D. vulgaris formed a scaffold for the biofilm, while intermediate and steady-state images revealed that M. maripaludis joined the biofilm later, likely in response to H(2) produced by the SRB. Close interactions in structured biofilm allowed efficient transfer of H(2) to M. maripaludis, and H(2) was only detected in cocultures with a mutant SRB that was deficient in biofilm formation (ΔpilA). M. maripaludis produced more carbohydrate (uronic acid, hexose, and pentose) as a monoculture compared to total coculture biofilm, and this suggested an altered carbon flux during syntrophy. The syntrophic biofilm was structured into ridges (∼300 × 50 μm) and models predicted lactate limitation at ∼50 μm biofilm depth. The biofilm had structure that likely facilitated mass transfer of H(2) and lactate, yet maximized biomass with a more even population composition (number of each organism) when compared to the bulk-phase community. Total biomass protein was equivalent in lactate-limited and lactate-excess conditions when a biofilm was present, but in the absence of biofilm, total biomass protein was significantly reduced. The results suggest that multispecies biofilms create an environment conducive to resource sharing, resulting in increased biomass retention, or carrying capacity, for cooperative populations.
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spelling pubmed-42660472015-01-06 Biofilm growth mode promotes maximum carrying capacity and community stability during product inhibition syntrophy Brileya, Kristen A. Camilleri, Laura B. Zane, Grant M. Wall, Judy D. Fields, Matthew W. Front Microbiol Microbiology Sulfate-reducing bacteria (SRB) can interact syntrophically with other community members in the absence of sulfate, and interactions with hydrogen-consuming methanogens are beneficial when these archaea consume potentially inhibitory H(2) produced by the SRB. A dual continuous culture approach was used to characterize population structure within a syntrophic biofilm formed by the SRB Desulfovibrio vulgaris Hildenborough and the methanogenic archaeum Methanococcus maripaludis. Under the tested conditions, monocultures of D. vulgaris formed thin, stable biofilms, but monoculture M. maripaludis did not. Microscopy of intact syntrophic biofilm confirmed that D. vulgaris formed a scaffold for the biofilm, while intermediate and steady-state images revealed that M. maripaludis joined the biofilm later, likely in response to H(2) produced by the SRB. Close interactions in structured biofilm allowed efficient transfer of H(2) to M. maripaludis, and H(2) was only detected in cocultures with a mutant SRB that was deficient in biofilm formation (ΔpilA). M. maripaludis produced more carbohydrate (uronic acid, hexose, and pentose) as a monoculture compared to total coculture biofilm, and this suggested an altered carbon flux during syntrophy. The syntrophic biofilm was structured into ridges (∼300 × 50 μm) and models predicted lactate limitation at ∼50 μm biofilm depth. The biofilm had structure that likely facilitated mass transfer of H(2) and lactate, yet maximized biomass with a more even population composition (number of each organism) when compared to the bulk-phase community. Total biomass protein was equivalent in lactate-limited and lactate-excess conditions when a biofilm was present, but in the absence of biofilm, total biomass protein was significantly reduced. The results suggest that multispecies biofilms create an environment conducive to resource sharing, resulting in increased biomass retention, or carrying capacity, for cooperative populations. Frontiers Media S.A. 2014-12-15 /pmc/articles/PMC4266047/ /pubmed/25566209 http://dx.doi.org/10.3389/fmicb.2014.00693 Text en Copyright © 2014 Brileya, Camilleri, Zane, Wall and Fields. 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
Brileya, Kristen A.
Camilleri, Laura B.
Zane, Grant M.
Wall, Judy D.
Fields, Matthew W.
Biofilm growth mode promotes maximum carrying capacity and community stability during product inhibition syntrophy
title Biofilm growth mode promotes maximum carrying capacity and community stability during product inhibition syntrophy
title_full Biofilm growth mode promotes maximum carrying capacity and community stability during product inhibition syntrophy
title_fullStr Biofilm growth mode promotes maximum carrying capacity and community stability during product inhibition syntrophy
title_full_unstemmed Biofilm growth mode promotes maximum carrying capacity and community stability during product inhibition syntrophy
title_short Biofilm growth mode promotes maximum carrying capacity and community stability during product inhibition syntrophy
title_sort biofilm growth mode promotes maximum carrying capacity and community stability during product inhibition syntrophy
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4266047/
https://www.ncbi.nlm.nih.gov/pubmed/25566209
http://dx.doi.org/10.3389/fmicb.2014.00693
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