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Non-essentiality of canonical cell division genes in the planctomycete Planctopirus limnophila

Most bacteria divide by binary fission using an FtsZ-based mechanism that relies on a multi-protein complex, the divisome. In the majority of non-spherical bacteria another multi-protein complex, the elongasome, is also required for the maintenance of cell shape. Components of these multi-protein as...

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Autores principales: Rivas-Marin, Elena, Peeters, Stijn H., Claret Fernández, Laura, Jogler, Christian, van Niftrik, Laura, Wiegand, Sandra, Devos, Damien P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6952346/
https://www.ncbi.nlm.nih.gov/pubmed/31919386
http://dx.doi.org/10.1038/s41598-019-56978-8
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author Rivas-Marin, Elena
Peeters, Stijn H.
Claret Fernández, Laura
Jogler, Christian
van Niftrik, Laura
Wiegand, Sandra
Devos, Damien P.
author_facet Rivas-Marin, Elena
Peeters, Stijn H.
Claret Fernández, Laura
Jogler, Christian
van Niftrik, Laura
Wiegand, Sandra
Devos, Damien P.
author_sort Rivas-Marin, Elena
collection PubMed
description Most bacteria divide by binary fission using an FtsZ-based mechanism that relies on a multi-protein complex, the divisome. In the majority of non-spherical bacteria another multi-protein complex, the elongasome, is also required for the maintenance of cell shape. Components of these multi-protein assemblies are conserved and essential in most bacteria. Here, we provide evidence that at least three proteins of these two complexes are not essential in the FtsZ-less ovoid planctomycete bacterium Planctopirus limnophila which divides by budding. We attempted to construct P. limnophila knock-out mutants of the genes coding for the divisome proteins FtsI, FtsK, FtsW and the elongasome protein MreB. Surprisingly, ftsI, ftsW and mreB could be deleted without affecting the growth rate. On the other hand, the conserved ftsK appeared to be essential in this bacterium. In conclusion, the canonical bacterial cell division machinery is not essential in P. limnophila and this bacterium divides via budding using an unknown mechanism.
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spelling pubmed-69523462020-01-13 Non-essentiality of canonical cell division genes in the planctomycete Planctopirus limnophila Rivas-Marin, Elena Peeters, Stijn H. Claret Fernández, Laura Jogler, Christian van Niftrik, Laura Wiegand, Sandra Devos, Damien P. Sci Rep Article Most bacteria divide by binary fission using an FtsZ-based mechanism that relies on a multi-protein complex, the divisome. In the majority of non-spherical bacteria another multi-protein complex, the elongasome, is also required for the maintenance of cell shape. Components of these multi-protein assemblies are conserved and essential in most bacteria. Here, we provide evidence that at least three proteins of these two complexes are not essential in the FtsZ-less ovoid planctomycete bacterium Planctopirus limnophila which divides by budding. We attempted to construct P. limnophila knock-out mutants of the genes coding for the divisome proteins FtsI, FtsK, FtsW and the elongasome protein MreB. Surprisingly, ftsI, ftsW and mreB could be deleted without affecting the growth rate. On the other hand, the conserved ftsK appeared to be essential in this bacterium. In conclusion, the canonical bacterial cell division machinery is not essential in P. limnophila and this bacterium divides via budding using an unknown mechanism. Nature Publishing Group UK 2020-01-09 /pmc/articles/PMC6952346/ /pubmed/31919386 http://dx.doi.org/10.1038/s41598-019-56978-8 Text en © The Author(s) 2020 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
Rivas-Marin, Elena
Peeters, Stijn H.
Claret Fernández, Laura
Jogler, Christian
van Niftrik, Laura
Wiegand, Sandra
Devos, Damien P.
Non-essentiality of canonical cell division genes in the planctomycete Planctopirus limnophila
title Non-essentiality of canonical cell division genes in the planctomycete Planctopirus limnophila
title_full Non-essentiality of canonical cell division genes in the planctomycete Planctopirus limnophila
title_fullStr Non-essentiality of canonical cell division genes in the planctomycete Planctopirus limnophila
title_full_unstemmed Non-essentiality of canonical cell division genes in the planctomycete Planctopirus limnophila
title_short Non-essentiality of canonical cell division genes in the planctomycete Planctopirus limnophila
title_sort non-essentiality of canonical cell division genes in the planctomycete planctopirus limnophila
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6952346/
https://www.ncbi.nlm.nih.gov/pubmed/31919386
http://dx.doi.org/10.1038/s41598-019-56978-8
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