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How haptophytes microalgae mitigate vitamin B(12) limitation

Vitamin B(12) (cobalamin) can control phytoplankton development and community composition, with around half of microalgal species requiring this vitamin for growth. B(12) dependency is determined by the absence of cobalamin-independent methionine synthase and is unrelated across lineages. Despite th...

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Autores principales: Nef, Charlotte, Jung, Sébastien, Mairet, Francis, Kaas, Raymond, Grizeau, Dominique, Garnier, Matthieu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6557843/
https://www.ncbi.nlm.nih.gov/pubmed/31182768
http://dx.doi.org/10.1038/s41598-019-44797-w
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author Nef, Charlotte
Jung, Sébastien
Mairet, Francis
Kaas, Raymond
Grizeau, Dominique
Garnier, Matthieu
author_facet Nef, Charlotte
Jung, Sébastien
Mairet, Francis
Kaas, Raymond
Grizeau, Dominique
Garnier, Matthieu
author_sort Nef, Charlotte
collection PubMed
description Vitamin B(12) (cobalamin) can control phytoplankton development and community composition, with around half of microalgal species requiring this vitamin for growth. B(12) dependency is determined by the absence of cobalamin-independent methionine synthase and is unrelated across lineages. Despite their important role in carbon and sulphur biogeochemistry, little is known about haptophytes utilization of vitamin B(12) and their ability to cope with its limitation. Here we report the first evaluation of B(12) auxotrophy among this lineage based on molecular data of 19 species from 9 families. We assume that all species encode only a B(12)-dependent methionine synthase, suggesting ubiquitous B(12) auxotrophy in this phylum. We further address the effect of different B(12) limitations on the molecular physiology of the model haptophyte Tisochrysis lutea. By coupling growth assays in batch and chemostat to cobalamin quantification and expression analyses, we propose that haptophytes use three strategies to cope with B(12) limitation. Haptophytes may assimilate dissolved methionine, finely regulate genes involved in methionine cycle and B(12) transport and/or limit B(12) transport to the mitochondrion. Taken together, these results provide better understanding of B(12) metabolism in haptophytes and represent valuable data for deciphering how B(12)-producing bacteria shape the structure and dynamics of this important phytoplankton community.
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spelling pubmed-65578432019-06-19 How haptophytes microalgae mitigate vitamin B(12) limitation Nef, Charlotte Jung, Sébastien Mairet, Francis Kaas, Raymond Grizeau, Dominique Garnier, Matthieu Sci Rep Article Vitamin B(12) (cobalamin) can control phytoplankton development and community composition, with around half of microalgal species requiring this vitamin for growth. B(12) dependency is determined by the absence of cobalamin-independent methionine synthase and is unrelated across lineages. Despite their important role in carbon and sulphur biogeochemistry, little is known about haptophytes utilization of vitamin B(12) and their ability to cope with its limitation. Here we report the first evaluation of B(12) auxotrophy among this lineage based on molecular data of 19 species from 9 families. We assume that all species encode only a B(12)-dependent methionine synthase, suggesting ubiquitous B(12) auxotrophy in this phylum. We further address the effect of different B(12) limitations on the molecular physiology of the model haptophyte Tisochrysis lutea. By coupling growth assays in batch and chemostat to cobalamin quantification and expression analyses, we propose that haptophytes use three strategies to cope with B(12) limitation. Haptophytes may assimilate dissolved methionine, finely regulate genes involved in methionine cycle and B(12) transport and/or limit B(12) transport to the mitochondrion. Taken together, these results provide better understanding of B(12) metabolism in haptophytes and represent valuable data for deciphering how B(12)-producing bacteria shape the structure and dynamics of this important phytoplankton community. Nature Publishing Group UK 2019-06-10 /pmc/articles/PMC6557843/ /pubmed/31182768 http://dx.doi.org/10.1038/s41598-019-44797-w Text en © The Author(s) 2019 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
Nef, Charlotte
Jung, Sébastien
Mairet, Francis
Kaas, Raymond
Grizeau, Dominique
Garnier, Matthieu
How haptophytes microalgae mitigate vitamin B(12) limitation
title How haptophytes microalgae mitigate vitamin B(12) limitation
title_full How haptophytes microalgae mitigate vitamin B(12) limitation
title_fullStr How haptophytes microalgae mitigate vitamin B(12) limitation
title_full_unstemmed How haptophytes microalgae mitigate vitamin B(12) limitation
title_short How haptophytes microalgae mitigate vitamin B(12) limitation
title_sort how haptophytes microalgae mitigate vitamin b(12) limitation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6557843/
https://www.ncbi.nlm.nih.gov/pubmed/31182768
http://dx.doi.org/10.1038/s41598-019-44797-w
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