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An alternative polysaccharide uptake mechanism of marine bacteria

Heterotrophic microbial communities process much of the carbon fixed by phytoplankton in the ocean, thus having a critical role in the global carbon cycle. A major fraction of the phytoplankton-derived substrates are high-molecular-weight (HMW) polysaccharides. For bacterial uptake, these substrates...

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Autores principales: Reintjes, Greta, Arnosti, Carol, Fuchs, Bernhard M, Amann, Rudolf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5520146/
https://www.ncbi.nlm.nih.gov/pubmed/28323277
http://dx.doi.org/10.1038/ismej.2017.26
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author Reintjes, Greta
Arnosti, Carol
Fuchs, Bernhard M
Amann, Rudolf
author_facet Reintjes, Greta
Arnosti, Carol
Fuchs, Bernhard M
Amann, Rudolf
author_sort Reintjes, Greta
collection PubMed
description Heterotrophic microbial communities process much of the carbon fixed by phytoplankton in the ocean, thus having a critical role in the global carbon cycle. A major fraction of the phytoplankton-derived substrates are high-molecular-weight (HMW) polysaccharides. For bacterial uptake, these substrates must initially be hydrolysed to smaller sizes by extracellular enzymes. We investigated polysaccharide hydrolysis by microbial communities during a transect of the Atlantic Ocean, and serendipitously discovered—using super-resolution structured illumination microscopy—that up to 26% of total cells showed uptake of fluorescently labelled polysaccharides (FLA-PS). Fluorescence in situ hybridisation identified these organisms as members of the bacterial phyla Bacteroidetes and Planctomycetes and the gammaproteobacterial genus Catenovulum. Simultaneous membrane staining with nile red indicated that the FLA-PS labelling occurred in the cell but not in the cytoplasm. The dynamics of FLA-PS staining was further investigated in pure culture experiments using Gramella forsetii, a marine member of Bacteroidetes. The staining patterns observed in environmental samples and pure culture tests are consistent with a ‘selfish’ uptake mechanisms of larger oligosaccharides (>600 Da), as demonstrated for gut Bacteroidetes. Ecologically, this alternative polysaccharide uptake mechanism secures substantial quantities of substrate in the periplasmic space, where further processing can occur without diffusive loss. Such a mechanism challenges the paradigm that hydrolysis of HMW substrates inevitably yields low-molecular-weight fragments that are available to the surrounding community and demonstrates the importance of an alternative mechanism of polysaccharide uptake in marine bacteria.
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spelling pubmed-55201462017-10-12 An alternative polysaccharide uptake mechanism of marine bacteria Reintjes, Greta Arnosti, Carol Fuchs, Bernhard M Amann, Rudolf ISME J Original Article Heterotrophic microbial communities process much of the carbon fixed by phytoplankton in the ocean, thus having a critical role in the global carbon cycle. A major fraction of the phytoplankton-derived substrates are high-molecular-weight (HMW) polysaccharides. For bacterial uptake, these substrates must initially be hydrolysed to smaller sizes by extracellular enzymes. We investigated polysaccharide hydrolysis by microbial communities during a transect of the Atlantic Ocean, and serendipitously discovered—using super-resolution structured illumination microscopy—that up to 26% of total cells showed uptake of fluorescently labelled polysaccharides (FLA-PS). Fluorescence in situ hybridisation identified these organisms as members of the bacterial phyla Bacteroidetes and Planctomycetes and the gammaproteobacterial genus Catenovulum. Simultaneous membrane staining with nile red indicated that the FLA-PS labelling occurred in the cell but not in the cytoplasm. The dynamics of FLA-PS staining was further investigated in pure culture experiments using Gramella forsetii, a marine member of Bacteroidetes. The staining patterns observed in environmental samples and pure culture tests are consistent with a ‘selfish’ uptake mechanisms of larger oligosaccharides (>600 Da), as demonstrated for gut Bacteroidetes. Ecologically, this alternative polysaccharide uptake mechanism secures substantial quantities of substrate in the periplasmic space, where further processing can occur without diffusive loss. Such a mechanism challenges the paradigm that hydrolysis of HMW substrates inevitably yields low-molecular-weight fragments that are available to the surrounding community and demonstrates the importance of an alternative mechanism of polysaccharide uptake in marine bacteria. Nature Publishing Group 2017-07 2017-03-21 /pmc/articles/PMC5520146/ /pubmed/28323277 http://dx.doi.org/10.1038/ismej.2017.26 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Original Article
Reintjes, Greta
Arnosti, Carol
Fuchs, Bernhard M
Amann, Rudolf
An alternative polysaccharide uptake mechanism of marine bacteria
title An alternative polysaccharide uptake mechanism of marine bacteria
title_full An alternative polysaccharide uptake mechanism of marine bacteria
title_fullStr An alternative polysaccharide uptake mechanism of marine bacteria
title_full_unstemmed An alternative polysaccharide uptake mechanism of marine bacteria
title_short An alternative polysaccharide uptake mechanism of marine bacteria
title_sort alternative polysaccharide uptake mechanism of marine bacteria
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5520146/
https://www.ncbi.nlm.nih.gov/pubmed/28323277
http://dx.doi.org/10.1038/ismej.2017.26
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