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Antarctic marine ciliates under stress: superoxide dismutases from the psychrophilic Euplotes focardii are cold-active yet heat tolerant enzymes

Oxidative stress is a particularly severe threat to Antarctic marine polar organisms because they are exposed to high dissolved oxygen and to intense UV radiation. This paper reports the features of three superoxide dismutases from the Antarctic psychrophilic ciliate Euplotes focardii that faces two...

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Autores principales: Pischedda, Alessandro, Ramasamy, Kesava Priyan, Mangiagalli, Marco, Chiappori, Federica, Milanesi, Luciano, Miceli, Cristina, Pucciarelli, Sandra, Lotti, Marina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6170424/
https://www.ncbi.nlm.nih.gov/pubmed/30283056
http://dx.doi.org/10.1038/s41598-018-33127-1
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author Pischedda, Alessandro
Ramasamy, Kesava Priyan
Mangiagalli, Marco
Chiappori, Federica
Milanesi, Luciano
Miceli, Cristina
Pucciarelli, Sandra
Lotti, Marina
author_facet Pischedda, Alessandro
Ramasamy, Kesava Priyan
Mangiagalli, Marco
Chiappori, Federica
Milanesi, Luciano
Miceli, Cristina
Pucciarelli, Sandra
Lotti, Marina
author_sort Pischedda, Alessandro
collection PubMed
description Oxidative stress is a particularly severe threat to Antarctic marine polar organisms because they are exposed to high dissolved oxygen and to intense UV radiation. This paper reports the features of three superoxide dismutases from the Antarctic psychrophilic ciliate Euplotes focardii that faces two environmental challenges, oxidative stress and low temperature. Two out of these are Cu,Zn superoxide dismutases (named Ef-SOD1a and Ef-SOD1b) and one belongs to the Mn-containing group (Ef-SOD2). Ef-SOD1s and Ef-SOD2 differ in their evolutionary history, expression and overall structural features. Ef-SOD1 genes are expressed at different levels, with Ef-SOD1b mRNA 20-fold higher at the ciliate optimal temperature of growth (4 °C). All Ef-SOD enzymes are active at 4 °C, consistent with the definition of cold-adapted enzymes. At the same time, they display temperatures of melting in the range 50–70 °C and retain residual activity after incubation at 65–75 °C. Supported by data of molecular dynamics simulation, we conclude that the E. focardii SODs combine cold activity, local molecular flexibility and thermo tolerance.
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spelling pubmed-61704242018-10-05 Antarctic marine ciliates under stress: superoxide dismutases from the psychrophilic Euplotes focardii are cold-active yet heat tolerant enzymes Pischedda, Alessandro Ramasamy, Kesava Priyan Mangiagalli, Marco Chiappori, Federica Milanesi, Luciano Miceli, Cristina Pucciarelli, Sandra Lotti, Marina Sci Rep Article Oxidative stress is a particularly severe threat to Antarctic marine polar organisms because they are exposed to high dissolved oxygen and to intense UV radiation. This paper reports the features of three superoxide dismutases from the Antarctic psychrophilic ciliate Euplotes focardii that faces two environmental challenges, oxidative stress and low temperature. Two out of these are Cu,Zn superoxide dismutases (named Ef-SOD1a and Ef-SOD1b) and one belongs to the Mn-containing group (Ef-SOD2). Ef-SOD1s and Ef-SOD2 differ in their evolutionary history, expression and overall structural features. Ef-SOD1 genes are expressed at different levels, with Ef-SOD1b mRNA 20-fold higher at the ciliate optimal temperature of growth (4 °C). All Ef-SOD enzymes are active at 4 °C, consistent with the definition of cold-adapted enzymes. At the same time, they display temperatures of melting in the range 50–70 °C and retain residual activity after incubation at 65–75 °C. Supported by data of molecular dynamics simulation, we conclude that the E. focardii SODs combine cold activity, local molecular flexibility and thermo tolerance. Nature Publishing Group UK 2018-10-03 /pmc/articles/PMC6170424/ /pubmed/30283056 http://dx.doi.org/10.1038/s41598-018-33127-1 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Pischedda, Alessandro
Ramasamy, Kesava Priyan
Mangiagalli, Marco
Chiappori, Federica
Milanesi, Luciano
Miceli, Cristina
Pucciarelli, Sandra
Lotti, Marina
Antarctic marine ciliates under stress: superoxide dismutases from the psychrophilic Euplotes focardii are cold-active yet heat tolerant enzymes
title Antarctic marine ciliates under stress: superoxide dismutases from the psychrophilic Euplotes focardii are cold-active yet heat tolerant enzymes
title_full Antarctic marine ciliates under stress: superoxide dismutases from the psychrophilic Euplotes focardii are cold-active yet heat tolerant enzymes
title_fullStr Antarctic marine ciliates under stress: superoxide dismutases from the psychrophilic Euplotes focardii are cold-active yet heat tolerant enzymes
title_full_unstemmed Antarctic marine ciliates under stress: superoxide dismutases from the psychrophilic Euplotes focardii are cold-active yet heat tolerant enzymes
title_short Antarctic marine ciliates under stress: superoxide dismutases from the psychrophilic Euplotes focardii are cold-active yet heat tolerant enzymes
title_sort antarctic marine ciliates under stress: superoxide dismutases from the psychrophilic euplotes focardii are cold-active yet heat tolerant enzymes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6170424/
https://www.ncbi.nlm.nih.gov/pubmed/30283056
http://dx.doi.org/10.1038/s41598-018-33127-1
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