Cargando…

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....

Descripción completa

Detalles Bibliográficos
Autores principales: Ramijan, Karina, Zhang, Zheren, van Wezel, Gilles P., Claessen, Dennis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
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
_version_ 1783527356048080896
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
work_keys_str_mv AT ramijankarina genomerearrangementsandmegaplasmidlossinthefilamentousbacteriumkitasatosporaviridifaciensareassociatedwithprotoplastformationandregeneration
AT zhangzheren genomerearrangementsandmegaplasmidlossinthefilamentousbacteriumkitasatosporaviridifaciensareassociatedwithprotoplastformationandregeneration
AT vanwezelgillesp genomerearrangementsandmegaplasmidlossinthefilamentousbacteriumkitasatosporaviridifaciensareassociatedwithprotoplastformationandregeneration
AT claessendennis genomerearrangementsandmegaplasmidlossinthefilamentousbacteriumkitasatosporaviridifaciensareassociatedwithprotoplastformationandregeneration