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Adaptive laboratory evolution of Corynebacterium glutamicum towards higher growth rates on glucose minimal medium
In this work, we performed a comparative adaptive laboratory evolution experiment of the important biotechnological platform strain Corynebacterium glutamicum ATCC 13032 and its prophage-free variant MB001 towards improved growth rates on glucose minimal medium. Both strains displayed a comparable a...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5711897/ https://www.ncbi.nlm.nih.gov/pubmed/29196644 http://dx.doi.org/10.1038/s41598-017-17014-9 |
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author | Pfeifer, Eugen Gätgens, Cornelia Polen, Tino Frunzke, Julia |
author_facet | Pfeifer, Eugen Gätgens, Cornelia Polen, Tino Frunzke, Julia |
author_sort | Pfeifer, Eugen |
collection | PubMed |
description | In this work, we performed a comparative adaptive laboratory evolution experiment of the important biotechnological platform strain Corynebacterium glutamicum ATCC 13032 and its prophage-free variant MB001 towards improved growth rates on glucose minimal medium. Both strains displayed a comparable adaptation behavior and no significant differences in genomic rearrangements and mutation frequencies. Remarkably, a significant fitness leap by about 20% was observed for both strains already after 100 generations. Isolated top clones (UBw and UBm) showed an about 26% increased growth rate on glucose minimal medium. Genome sequencing of evolved clones and populations resulted in the identification of key mutations in pyk (pyruvate kinase), fruK (1-phosphofructokinase) and corA encoding a Mg(2+) importer. The reintegration of selected pyk and fruK mutations resulted in an increased glucose consumption rate and ptsG expression causative for the accelerated growth on glucose minimal medium, whereas corA mutations improved growth under Mg(2+) limiting conditions. Overall, this study resulted in the identification of causative key mutations improving the growth of C. glutamicum on glucose. These identified mutational hot spots as well as the two evolved top strains, UBw and UBm, represent promising targets for future metabolic engineering approaches. |
format | Online Article Text |
id | pubmed-5711897 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57118972017-12-06 Adaptive laboratory evolution of Corynebacterium glutamicum towards higher growth rates on glucose minimal medium Pfeifer, Eugen Gätgens, Cornelia Polen, Tino Frunzke, Julia Sci Rep Article In this work, we performed a comparative adaptive laboratory evolution experiment of the important biotechnological platform strain Corynebacterium glutamicum ATCC 13032 and its prophage-free variant MB001 towards improved growth rates on glucose minimal medium. Both strains displayed a comparable adaptation behavior and no significant differences in genomic rearrangements and mutation frequencies. Remarkably, a significant fitness leap by about 20% was observed for both strains already after 100 generations. Isolated top clones (UBw and UBm) showed an about 26% increased growth rate on glucose minimal medium. Genome sequencing of evolved clones and populations resulted in the identification of key mutations in pyk (pyruvate kinase), fruK (1-phosphofructokinase) and corA encoding a Mg(2+) importer. The reintegration of selected pyk and fruK mutations resulted in an increased glucose consumption rate and ptsG expression causative for the accelerated growth on glucose minimal medium, whereas corA mutations improved growth under Mg(2+) limiting conditions. Overall, this study resulted in the identification of causative key mutations improving the growth of C. glutamicum on glucose. These identified mutational hot spots as well as the two evolved top strains, UBw and UBm, represent promising targets for future metabolic engineering approaches. Nature Publishing Group UK 2017-12-01 /pmc/articles/PMC5711897/ /pubmed/29196644 http://dx.doi.org/10.1038/s41598-017-17014-9 Text en © The Author(s) 2017 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 Pfeifer, Eugen Gätgens, Cornelia Polen, Tino Frunzke, Julia Adaptive laboratory evolution of Corynebacterium glutamicum towards higher growth rates on glucose minimal medium |
title | Adaptive laboratory evolution of Corynebacterium glutamicum towards higher growth rates on glucose minimal medium |
title_full | Adaptive laboratory evolution of Corynebacterium glutamicum towards higher growth rates on glucose minimal medium |
title_fullStr | Adaptive laboratory evolution of Corynebacterium glutamicum towards higher growth rates on glucose minimal medium |
title_full_unstemmed | Adaptive laboratory evolution of Corynebacterium glutamicum towards higher growth rates on glucose minimal medium |
title_short | Adaptive laboratory evolution of Corynebacterium glutamicum towards higher growth rates on glucose minimal medium |
title_sort | adaptive laboratory evolution of corynebacterium glutamicum towards higher growth rates on glucose minimal medium |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5711897/ https://www.ncbi.nlm.nih.gov/pubmed/29196644 http://dx.doi.org/10.1038/s41598-017-17014-9 |
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