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Functional distinctness in the exoproteomes of marine S ynechococcus
The exported protein fraction of an organism may reflect its life strategy and, ultimately, the way it is perceived by the outside world. Bioinformatic prediction of the exported pan‐proteome of P rochlorococcus and S ynechococcus lineages demonstrated that (i) this fraction of the encoded proteome...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4949707/ https://www.ncbi.nlm.nih.gov/pubmed/25727668 http://dx.doi.org/10.1111/1462-2920.12822 |
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author | Christie‐Oleza, Joseph A. Armengaud, Jean Guerin, Philippe Scanlan, David J. |
author_facet | Christie‐Oleza, Joseph A. Armengaud, Jean Guerin, Philippe Scanlan, David J. |
author_sort | Christie‐Oleza, Joseph A. |
collection | PubMed |
description | The exported protein fraction of an organism may reflect its life strategy and, ultimately, the way it is perceived by the outside world. Bioinformatic prediction of the exported pan‐proteome of P rochlorococcus and S ynechococcus lineages demonstrated that (i) this fraction of the encoded proteome had a much higher incidence of lineage‐specific proteins than the cytosolic fraction (57% and 73% homologue incidence respectively) and (ii) exported proteins are largely uncharacterized to date (54%) compared with proteins from the cytosolic fraction (35%). This suggests that the genomic and functional diversity of these organisms lies largely in the diverse pool of novel functions these organisms export to/through their membranes playing a key role in community diversification, e.g. for niche partitioning or evading predation. Experimental exoproteome analysis of marine S ynechococcus showed transport systems for inorganic nutrients, an interesting array of strain‐specific exoproteins involved in mutualistic or hostile interactions (i.e. hemolysins, pilins, adhesins), and exoenzymes with a potential mixotrophic goal (i.e. exoproteases and chitinases). We also show how these organisms can remodel their exoproteome, i.e. by increasing the repertoire of interaction proteins when grown in the presence of a heterotroph or decrease exposure to prey when grown in the dark. Finally, our data indicate that heterotrophic bacteria can feed on the exoproteome of S ynechococcus. |
format | Online Article Text |
id | pubmed-4949707 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-49497072016-07-28 Functional distinctness in the exoproteomes of marine S ynechococcus Christie‐Oleza, Joseph A. Armengaud, Jean Guerin, Philippe Scanlan, David J. Environ Microbiol Research Articles The exported protein fraction of an organism may reflect its life strategy and, ultimately, the way it is perceived by the outside world. Bioinformatic prediction of the exported pan‐proteome of P rochlorococcus and S ynechococcus lineages demonstrated that (i) this fraction of the encoded proteome had a much higher incidence of lineage‐specific proteins than the cytosolic fraction (57% and 73% homologue incidence respectively) and (ii) exported proteins are largely uncharacterized to date (54%) compared with proteins from the cytosolic fraction (35%). This suggests that the genomic and functional diversity of these organisms lies largely in the diverse pool of novel functions these organisms export to/through their membranes playing a key role in community diversification, e.g. for niche partitioning or evading predation. Experimental exoproteome analysis of marine S ynechococcus showed transport systems for inorganic nutrients, an interesting array of strain‐specific exoproteins involved in mutualistic or hostile interactions (i.e. hemolysins, pilins, adhesins), and exoenzymes with a potential mixotrophic goal (i.e. exoproteases and chitinases). We also show how these organisms can remodel their exoproteome, i.e. by increasing the repertoire of interaction proteins when grown in the presence of a heterotroph or decrease exposure to prey when grown in the dark. Finally, our data indicate that heterotrophic bacteria can feed on the exoproteome of S ynechococcus. John Wiley and Sons Inc. 2015-04-15 2015-10 /pmc/articles/PMC4949707/ /pubmed/25727668 http://dx.doi.org/10.1111/1462-2920.12822 Text en © 2015 The Authors. Environmental Microbiology published by Society for Applied Microbiology and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Christie‐Oleza, Joseph A. Armengaud, Jean Guerin, Philippe Scanlan, David J. Functional distinctness in the exoproteomes of marine S ynechococcus |
title | Functional distinctness in the exoproteomes of marine S
ynechococcus
|
title_full | Functional distinctness in the exoproteomes of marine S
ynechococcus
|
title_fullStr | Functional distinctness in the exoproteomes of marine S
ynechococcus
|
title_full_unstemmed | Functional distinctness in the exoproteomes of marine S
ynechococcus
|
title_short | Functional distinctness in the exoproteomes of marine S
ynechococcus
|
title_sort | functional distinctness in the exoproteomes of marine s
ynechococcus |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4949707/ https://www.ncbi.nlm.nih.gov/pubmed/25727668 http://dx.doi.org/10.1111/1462-2920.12822 |
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