Cargando…

Osmoadaptative Strategy and Its Molecular Signature in Obligately Halophilic Heterotrophic Protists

Halophilic microbes living in hypersaline environments must counteract the detrimental effects of low water activity and salt interference. Some halophilic prokaryotes equilibrate their intracellular osmotic strength with the extracellular milieu by importing inorganic solutes, mainly potassium. The...

Descripción completa

Detalles Bibliográficos
Autores principales: Harding, Tommy, Brown, Matthew W., Simpson, Alastair G.B., Roger, Andrew J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4987115/
https://www.ncbi.nlm.nih.gov/pubmed/27412608
http://dx.doi.org/10.1093/gbe/evw152
_version_ 1782448268415860736
author Harding, Tommy
Brown, Matthew W.
Simpson, Alastair G.B.
Roger, Andrew J.
author_facet Harding, Tommy
Brown, Matthew W.
Simpson, Alastair G.B.
Roger, Andrew J.
author_sort Harding, Tommy
collection PubMed
description Halophilic microbes living in hypersaline environments must counteract the detrimental effects of low water activity and salt interference. Some halophilic prokaryotes equilibrate their intracellular osmotic strength with the extracellular milieu by importing inorganic solutes, mainly potassium. These “salt-in” organisms characteristically have proteins that are highly enriched with acidic and hydrophilic residues. In contrast, “salt-out” halophiles accumulate large amounts of organic solutes like amino acids, sugars and polyols, and lack a strong signature of halophilicity in the amino acid composition of cytoplasmic proteins. Studies to date have examined halophilic prokaryotes, yeasts, or algae, thus virtually nothing is known about the molecular adaptations of the other eukaryotic microbes, that is, heterotrophic protists (protozoa), that also thrive in hypersaline habitats. We conducted transcriptomic investigations to unravel the molecular adaptations of two obligately halophilic protists, Halocafeteria seosinensis and Pharyngomonas kirbyi. Their predicted cytoplasmic proteomes showed increased hydrophilicity compared with marine protists. Furthermore, analysis of reconstructed ancestral sequences suggested that, relative to mesophiles, proteins in halophilic protists have undergone fewer substitutions from hydrophilic to hydrophobic residues since divergence from their closest relatives. These results suggest that these halophilic protists have a higher intracellular salt content than marine protists. However, absence of the acidic signature of salt-in microbes suggests that Haloc. seosinensis and P. kirbyi utilize organic osmolytes to maintain osmotic equilibrium. We detected increased expression of enzymes involved in synthesis and transport of organic osmolytes, namely hydroxyectoine and myo-inositol, at maximal salt concentration for growth in Haloc. seosinensis, suggesting possible candidates for these inferred organic osmolytes.
format Online
Article
Text
id pubmed-4987115
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-49871152016-08-22 Osmoadaptative Strategy and Its Molecular Signature in Obligately Halophilic Heterotrophic Protists Harding, Tommy Brown, Matthew W. Simpson, Alastair G.B. Roger, Andrew J. Genome Biol Evol Research Article Halophilic microbes living in hypersaline environments must counteract the detrimental effects of low water activity and salt interference. Some halophilic prokaryotes equilibrate their intracellular osmotic strength with the extracellular milieu by importing inorganic solutes, mainly potassium. These “salt-in” organisms characteristically have proteins that are highly enriched with acidic and hydrophilic residues. In contrast, “salt-out” halophiles accumulate large amounts of organic solutes like amino acids, sugars and polyols, and lack a strong signature of halophilicity in the amino acid composition of cytoplasmic proteins. Studies to date have examined halophilic prokaryotes, yeasts, or algae, thus virtually nothing is known about the molecular adaptations of the other eukaryotic microbes, that is, heterotrophic protists (protozoa), that also thrive in hypersaline habitats. We conducted transcriptomic investigations to unravel the molecular adaptations of two obligately halophilic protists, Halocafeteria seosinensis and Pharyngomonas kirbyi. Their predicted cytoplasmic proteomes showed increased hydrophilicity compared with marine protists. Furthermore, analysis of reconstructed ancestral sequences suggested that, relative to mesophiles, proteins in halophilic protists have undergone fewer substitutions from hydrophilic to hydrophobic residues since divergence from their closest relatives. These results suggest that these halophilic protists have a higher intracellular salt content than marine protists. However, absence of the acidic signature of salt-in microbes suggests that Haloc. seosinensis and P. kirbyi utilize organic osmolytes to maintain osmotic equilibrium. We detected increased expression of enzymes involved in synthesis and transport of organic osmolytes, namely hydroxyectoine and myo-inositol, at maximal salt concentration for growth in Haloc. seosinensis, suggesting possible candidates for these inferred organic osmolytes. Oxford University Press 2016-07-12 /pmc/articles/PMC4987115/ /pubmed/27412608 http://dx.doi.org/10.1093/gbe/evw152 Text en © The Author 2016. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Harding, Tommy
Brown, Matthew W.
Simpson, Alastair G.B.
Roger, Andrew J.
Osmoadaptative Strategy and Its Molecular Signature in Obligately Halophilic Heterotrophic Protists
title Osmoadaptative Strategy and Its Molecular Signature in Obligately Halophilic Heterotrophic Protists
title_full Osmoadaptative Strategy and Its Molecular Signature in Obligately Halophilic Heterotrophic Protists
title_fullStr Osmoadaptative Strategy and Its Molecular Signature in Obligately Halophilic Heterotrophic Protists
title_full_unstemmed Osmoadaptative Strategy and Its Molecular Signature in Obligately Halophilic Heterotrophic Protists
title_short Osmoadaptative Strategy and Its Molecular Signature in Obligately Halophilic Heterotrophic Protists
title_sort osmoadaptative strategy and its molecular signature in obligately halophilic heterotrophic protists
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4987115/
https://www.ncbi.nlm.nih.gov/pubmed/27412608
http://dx.doi.org/10.1093/gbe/evw152
work_keys_str_mv AT hardingtommy osmoadaptativestrategyanditsmolecularsignatureinobligatelyhalophilicheterotrophicprotists
AT brownmattheww osmoadaptativestrategyanditsmolecularsignatureinobligatelyhalophilicheterotrophicprotists
AT simpsonalastairgb osmoadaptativestrategyanditsmolecularsignatureinobligatelyhalophilicheterotrophicprotists
AT rogerandrewj osmoadaptativestrategyanditsmolecularsignatureinobligatelyhalophilicheterotrophicprotists