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Engineering artificial photosynthetic life-forms through endosymbiosis
The evolutionary origin of the photosynthetic eukaryotes drastically altered the evolution of complex lifeforms and impacted global ecology. The endosymbiotic theory suggests that photosynthetic eukaryotes evolved due to endosymbiosis between non-photosynthetic eukaryotic host cells and photosynthet...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9042829/ https://www.ncbi.nlm.nih.gov/pubmed/35474066 http://dx.doi.org/10.1038/s41467-022-29961-7 |
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author | Cournoyer, Jason E. Altman, Sarah D. Gao, Yang-le Wallace, Catherine L. Zhang, Dianwen Lo, Guo-Hsuen Haskin, Noah T. Mehta, Angad P. |
author_facet | Cournoyer, Jason E. Altman, Sarah D. Gao, Yang-le Wallace, Catherine L. Zhang, Dianwen Lo, Guo-Hsuen Haskin, Noah T. Mehta, Angad P. |
author_sort | Cournoyer, Jason E. |
collection | PubMed |
description | The evolutionary origin of the photosynthetic eukaryotes drastically altered the evolution of complex lifeforms and impacted global ecology. The endosymbiotic theory suggests that photosynthetic eukaryotes evolved due to endosymbiosis between non-photosynthetic eukaryotic host cells and photosynthetic cyanobacterial or algal endosymbionts. The photosynthetic endosymbionts, propagating within the cytoplasm of the host cells, evolved, and eventually transformed into chloroplasts. Despite the fundamental importance of this evolutionary event, we have minimal understanding of this remarkable evolutionary transformation. Here, we design and engineer artificial, genetically tractable, photosynthetic endosymbiosis between photosynthetic cyanobacteria and budding yeasts. We engineer various mutants of model photosynthetic cyanobacteria as endosymbionts within yeast cells where, the engineered cyanobacteria perform bioenergetic functions to support the growth of yeast cells under defined photosynthetic conditions. We anticipate that these genetically tractable endosymbiotic platforms can be used for evolutionary studies, particularly related to organelle evolution, and also for synthetic biology applications. |
format | Online Article Text |
id | pubmed-9042829 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-90428292022-04-28 Engineering artificial photosynthetic life-forms through endosymbiosis Cournoyer, Jason E. Altman, Sarah D. Gao, Yang-le Wallace, Catherine L. Zhang, Dianwen Lo, Guo-Hsuen Haskin, Noah T. Mehta, Angad P. Nat Commun Article The evolutionary origin of the photosynthetic eukaryotes drastically altered the evolution of complex lifeforms and impacted global ecology. The endosymbiotic theory suggests that photosynthetic eukaryotes evolved due to endosymbiosis between non-photosynthetic eukaryotic host cells and photosynthetic cyanobacterial or algal endosymbionts. The photosynthetic endosymbionts, propagating within the cytoplasm of the host cells, evolved, and eventually transformed into chloroplasts. Despite the fundamental importance of this evolutionary event, we have minimal understanding of this remarkable evolutionary transformation. Here, we design and engineer artificial, genetically tractable, photosynthetic endosymbiosis between photosynthetic cyanobacteria and budding yeasts. We engineer various mutants of model photosynthetic cyanobacteria as endosymbionts within yeast cells where, the engineered cyanobacteria perform bioenergetic functions to support the growth of yeast cells under defined photosynthetic conditions. We anticipate that these genetically tractable endosymbiotic platforms can be used for evolutionary studies, particularly related to organelle evolution, and also for synthetic biology applications. Nature Publishing Group UK 2022-04-26 /pmc/articles/PMC9042829/ /pubmed/35474066 http://dx.doi.org/10.1038/s41467-022-29961-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Cournoyer, Jason E. Altman, Sarah D. Gao, Yang-le Wallace, Catherine L. Zhang, Dianwen Lo, Guo-Hsuen Haskin, Noah T. Mehta, Angad P. Engineering artificial photosynthetic life-forms through endosymbiosis |
title | Engineering artificial photosynthetic life-forms through endosymbiosis |
title_full | Engineering artificial photosynthetic life-forms through endosymbiosis |
title_fullStr | Engineering artificial photosynthetic life-forms through endosymbiosis |
title_full_unstemmed | Engineering artificial photosynthetic life-forms through endosymbiosis |
title_short | Engineering artificial photosynthetic life-forms through endosymbiosis |
title_sort | engineering artificial photosynthetic life-forms through endosymbiosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9042829/ https://www.ncbi.nlm.nih.gov/pubmed/35474066 http://dx.doi.org/10.1038/s41467-022-29961-7 |
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