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Synthetic cell division via membrane-transforming molecular assemblies

Reproduction, i.e. the ability to produce new individuals from a parent organism, is a hallmark of living matter. Even the simplest forms of reproduction require cell division: attempts to create a designer cell therefore should include a synthetic cell division machinery. In this review, we will il...

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Detalles Bibliográficos
Autores principales: Kretschmer, Simon, Ganzinger, Kristina A., Franquelim, Henri G., Schwille, Petra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6533746/
https://www.ncbi.nlm.nih.gov/pubmed/31126285
http://dx.doi.org/10.1186/s12915-019-0665-1
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author Kretschmer, Simon
Ganzinger, Kristina A.
Franquelim, Henri G.
Schwille, Petra
author_facet Kretschmer, Simon
Ganzinger, Kristina A.
Franquelim, Henri G.
Schwille, Petra
author_sort Kretschmer, Simon
collection PubMed
description Reproduction, i.e. the ability to produce new individuals from a parent organism, is a hallmark of living matter. Even the simplest forms of reproduction require cell division: attempts to create a designer cell therefore should include a synthetic cell division machinery. In this review, we will illustrate how nature solves this task, describing membrane remodelling processes in general and focusing on bacterial cell division in particular. We discuss recent progress made in their in vitro reconstitution, identify open challenges, and suggest how purely synthetic building blocks could provide an additional and attractive route to creating artificial cell division machineries.
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spelling pubmed-65337462019-05-28 Synthetic cell division via membrane-transforming molecular assemblies Kretschmer, Simon Ganzinger, Kristina A. Franquelim, Henri G. Schwille, Petra BMC Biol Review Reproduction, i.e. the ability to produce new individuals from a parent organism, is a hallmark of living matter. Even the simplest forms of reproduction require cell division: attempts to create a designer cell therefore should include a synthetic cell division machinery. In this review, we will illustrate how nature solves this task, describing membrane remodelling processes in general and focusing on bacterial cell division in particular. We discuss recent progress made in their in vitro reconstitution, identify open challenges, and suggest how purely synthetic building blocks could provide an additional and attractive route to creating artificial cell division machineries. BioMed Central 2019-05-24 /pmc/articles/PMC6533746/ /pubmed/31126285 http://dx.doi.org/10.1186/s12915-019-0665-1 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Kretschmer, Simon
Ganzinger, Kristina A.
Franquelim, Henri G.
Schwille, Petra
Synthetic cell division via membrane-transforming molecular assemblies
title Synthetic cell division via membrane-transforming molecular assemblies
title_full Synthetic cell division via membrane-transforming molecular assemblies
title_fullStr Synthetic cell division via membrane-transforming molecular assemblies
title_full_unstemmed Synthetic cell division via membrane-transforming molecular assemblies
title_short Synthetic cell division via membrane-transforming molecular assemblies
title_sort synthetic cell division via membrane-transforming molecular assemblies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6533746/
https://www.ncbi.nlm.nih.gov/pubmed/31126285
http://dx.doi.org/10.1186/s12915-019-0665-1
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