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Adaptive engineering of a hyperthermophilic archaeon on CO and discovering the underlying mechanism by multi-omics analysis
The hyperthermophilic archaeon Thermococcus onnurineus NA1 can grow and produce H(2) on carbon monoxide (CO) and its H(2) production rates have been improved through metabolic engineering. In this study, we applied adaptive evolution to enhance H(2) productivity. After over 150 serial transfers onto...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4791640/ https://www.ncbi.nlm.nih.gov/pubmed/26975345 http://dx.doi.org/10.1038/srep22896 |
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author | Lee, Seong Hyuk Kim, Min-Sik Lee, Jae-Hak Kim, Tae Wan Bae, Seung Seob Lee, Sung-Mok Jung, Hae Chang Yang, Tae-Jun Choi, Ae Ran Cho, Yong-Jun Lee, Jung-Hyun Kwon, Kae Kyoung Lee, Hyun Sook Kang, Sung Gyun |
author_facet | Lee, Seong Hyuk Kim, Min-Sik Lee, Jae-Hak Kim, Tae Wan Bae, Seung Seob Lee, Sung-Mok Jung, Hae Chang Yang, Tae-Jun Choi, Ae Ran Cho, Yong-Jun Lee, Jung-Hyun Kwon, Kae Kyoung Lee, Hyun Sook Kang, Sung Gyun |
author_sort | Lee, Seong Hyuk |
collection | PubMed |
description | The hyperthermophilic archaeon Thermococcus onnurineus NA1 can grow and produce H(2) on carbon monoxide (CO) and its H(2) production rates have been improved through metabolic engineering. In this study, we applied adaptive evolution to enhance H(2) productivity. After over 150 serial transfers onto CO medium, cell density, CO consumption rate and H(2) production rate increased. The underlying mechanism for those physiological changes could be explained by using multi-omics approaches including genomic, transcriptomic and epigenomic analyses. A putative transcriptional regulator was newly identified to regulate the expression levels of genes related to CO oxidation. Transcriptome analysis revealed significant changes in the transcript levels of genes belonging to the categories of transcription, translation and energy metabolism. Our study presents the first genome-scale methylation pattern of hyperthermophilic archaea. Adaptive evolution led to highly enhanced H(2) productivity at high CO flow rates using synthesis gas produced from coal gasification. |
format | Online Article Text |
id | pubmed-4791640 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47916402016-03-16 Adaptive engineering of a hyperthermophilic archaeon on CO and discovering the underlying mechanism by multi-omics analysis Lee, Seong Hyuk Kim, Min-Sik Lee, Jae-Hak Kim, Tae Wan Bae, Seung Seob Lee, Sung-Mok Jung, Hae Chang Yang, Tae-Jun Choi, Ae Ran Cho, Yong-Jun Lee, Jung-Hyun Kwon, Kae Kyoung Lee, Hyun Sook Kang, Sung Gyun Sci Rep Article The hyperthermophilic archaeon Thermococcus onnurineus NA1 can grow and produce H(2) on carbon monoxide (CO) and its H(2) production rates have been improved through metabolic engineering. In this study, we applied adaptive evolution to enhance H(2) productivity. After over 150 serial transfers onto CO medium, cell density, CO consumption rate and H(2) production rate increased. The underlying mechanism for those physiological changes could be explained by using multi-omics approaches including genomic, transcriptomic and epigenomic analyses. A putative transcriptional regulator was newly identified to regulate the expression levels of genes related to CO oxidation. Transcriptome analysis revealed significant changes in the transcript levels of genes belonging to the categories of transcription, translation and energy metabolism. Our study presents the first genome-scale methylation pattern of hyperthermophilic archaea. Adaptive evolution led to highly enhanced H(2) productivity at high CO flow rates using synthesis gas produced from coal gasification. Nature Publishing Group 2016-03-15 /pmc/articles/PMC4791640/ /pubmed/26975345 http://dx.doi.org/10.1038/srep22896 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Lee, Seong Hyuk Kim, Min-Sik Lee, Jae-Hak Kim, Tae Wan Bae, Seung Seob Lee, Sung-Mok Jung, Hae Chang Yang, Tae-Jun Choi, Ae Ran Cho, Yong-Jun Lee, Jung-Hyun Kwon, Kae Kyoung Lee, Hyun Sook Kang, Sung Gyun Adaptive engineering of a hyperthermophilic archaeon on CO and discovering the underlying mechanism by multi-omics analysis |
title | Adaptive engineering of a hyperthermophilic archaeon on CO and discovering the underlying mechanism by multi-omics analysis |
title_full | Adaptive engineering of a hyperthermophilic archaeon on CO and discovering the underlying mechanism by multi-omics analysis |
title_fullStr | Adaptive engineering of a hyperthermophilic archaeon on CO and discovering the underlying mechanism by multi-omics analysis |
title_full_unstemmed | Adaptive engineering of a hyperthermophilic archaeon on CO and discovering the underlying mechanism by multi-omics analysis |
title_short | Adaptive engineering of a hyperthermophilic archaeon on CO and discovering the underlying mechanism by multi-omics analysis |
title_sort | adaptive engineering of a hyperthermophilic archaeon on co and discovering the underlying mechanism by multi-omics analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4791640/ https://www.ncbi.nlm.nih.gov/pubmed/26975345 http://dx.doi.org/10.1038/srep22896 |
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