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Genome rearrangements and megaplasmid loss in the filamentous bacterium Kitasatospora viridifaciens are associated with protoplast formation and regeneration
Filamentous Actinobacteria are multicellular bacteria with linear replicons. Kitasatospora viridifaciens DSM 40239 contains a linear 7.8 Mb chromosome and an autonomously replicating plasmid KVP1 of 1.7 Mb. Here we show that lysozyme-induced protoplast formation of the multinucleated mycelium of K....
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7188733/ https://www.ncbi.nlm.nih.gov/pubmed/32060816 http://dx.doi.org/10.1007/s10482-020-01393-7 |
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author | Ramijan, Karina Zhang, Zheren van Wezel, Gilles P. Claessen, Dennis |
author_facet | Ramijan, Karina Zhang, Zheren van Wezel, Gilles P. Claessen, Dennis |
author_sort | Ramijan, Karina |
collection | PubMed |
description | Filamentous Actinobacteria are multicellular bacteria with linear replicons. Kitasatospora viridifaciens DSM 40239 contains a linear 7.8 Mb chromosome and an autonomously replicating plasmid KVP1 of 1.7 Mb. Here we show that lysozyme-induced protoplast formation of the multinucleated mycelium of K. viridifaciens drives morphological diversity. Characterisation and sequencing of an individual revertant colony that had lost the ability to differentiate revealed that the strain had not only lost most of KVP1 but also carried deletions in the right arm of the chromosome. Strikingly, the deletion sites were preceded by insertion sequence elements, suggesting that the rearrangements may have been caused by replicative transposition and homologous recombination between both replicons. These data indicate that protoplast formation is a stressful process that can lead to profound genetic changes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10482-020-01393-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7188733 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-71887332020-05-04 Genome rearrangements and megaplasmid loss in the filamentous bacterium Kitasatospora viridifaciens are associated with protoplast formation and regeneration Ramijan, Karina Zhang, Zheren van Wezel, Gilles P. Claessen, Dennis Antonie Van Leeuwenhoek Original Paper Filamentous Actinobacteria are multicellular bacteria with linear replicons. Kitasatospora viridifaciens DSM 40239 contains a linear 7.8 Mb chromosome and an autonomously replicating plasmid KVP1 of 1.7 Mb. Here we show that lysozyme-induced protoplast formation of the multinucleated mycelium of K. viridifaciens drives morphological diversity. Characterisation and sequencing of an individual revertant colony that had lost the ability to differentiate revealed that the strain had not only lost most of KVP1 but also carried deletions in the right arm of the chromosome. Strikingly, the deletion sites were preceded by insertion sequence elements, suggesting that the rearrangements may have been caused by replicative transposition and homologous recombination between both replicons. These data indicate that protoplast formation is a stressful process that can lead to profound genetic changes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10482-020-01393-7) contains supplementary material, which is available to authorized users. Springer International Publishing 2020-02-14 2020 /pmc/articles/PMC7188733/ /pubmed/32060816 http://dx.doi.org/10.1007/s10482-020-01393-7 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Original Paper Ramijan, Karina Zhang, Zheren van Wezel, Gilles P. Claessen, Dennis Genome rearrangements and megaplasmid loss in the filamentous bacterium Kitasatospora viridifaciens are associated with protoplast formation and regeneration |
title | Genome rearrangements and megaplasmid loss in the filamentous bacterium Kitasatospora viridifaciens are associated with protoplast formation and regeneration |
title_full | Genome rearrangements and megaplasmid loss in the filamentous bacterium Kitasatospora viridifaciens are associated with protoplast formation and regeneration |
title_fullStr | Genome rearrangements and megaplasmid loss in the filamentous bacterium Kitasatospora viridifaciens are associated with protoplast formation and regeneration |
title_full_unstemmed | Genome rearrangements and megaplasmid loss in the filamentous bacterium Kitasatospora viridifaciens are associated with protoplast formation and regeneration |
title_short | Genome rearrangements and megaplasmid loss in the filamentous bacterium Kitasatospora viridifaciens are associated with protoplast formation and regeneration |
title_sort | genome rearrangements and megaplasmid loss in the filamentous bacterium kitasatospora viridifaciens are associated with protoplast formation and regeneration |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7188733/ https://www.ncbi.nlm.nih.gov/pubmed/32060816 http://dx.doi.org/10.1007/s10482-020-01393-7 |
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