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Methanol-dependent Escherichia coli strains with a complete ribulose monophosphate cycle
Methanol is a biotechnologically promising substitute for food and feed substrates since it can be produced renewably from electricity, water and CO(2). Although progress has been made towards establishing Escherichia coli as a platform organism for methanol conversion via the energy efficient ribul...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7588473/ https://www.ncbi.nlm.nih.gov/pubmed/33106470 http://dx.doi.org/10.1038/s41467-020-19235-5 |
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author | Keller, Philipp Noor, Elad Meyer, Fabian Reiter, Michael A. Anastassov, Stanislav Kiefer, Patrick Vorholt, Julia A. |
author_facet | Keller, Philipp Noor, Elad Meyer, Fabian Reiter, Michael A. Anastassov, Stanislav Kiefer, Patrick Vorholt, Julia A. |
author_sort | Keller, Philipp |
collection | PubMed |
description | Methanol is a biotechnologically promising substitute for food and feed substrates since it can be produced renewably from electricity, water and CO(2). Although progress has been made towards establishing Escherichia coli as a platform organism for methanol conversion via the energy efficient ribulose monophosphate (RuMP) cycle, engineering strains that rely solely on methanol as a carbon source remains challenging. Here, we apply flux balance analysis to comprehensively identify methanol-dependent strains with high potential for adaptive laboratory evolution. We further investigate two out of 1200 candidate strains, one with a deletion of fructose-1,6-bisphosphatase (fbp) and another with triosephosphate isomerase (tpiA) deleted. In contrast to previous reported methanol-dependent strains, both feature a complete RuMP cycle and incorporate methanol to a high degree, with up to 31 and 99% fractional incorporation into RuMP cycle metabolites. These strains represent ideal starting points for evolution towards a fully methylotrophic lifestyle. |
format | Online Article Text |
id | pubmed-7588473 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75884732020-11-10 Methanol-dependent Escherichia coli strains with a complete ribulose monophosphate cycle Keller, Philipp Noor, Elad Meyer, Fabian Reiter, Michael A. Anastassov, Stanislav Kiefer, Patrick Vorholt, Julia A. Nat Commun Article Methanol is a biotechnologically promising substitute for food and feed substrates since it can be produced renewably from electricity, water and CO(2). Although progress has been made towards establishing Escherichia coli as a platform organism for methanol conversion via the energy efficient ribulose monophosphate (RuMP) cycle, engineering strains that rely solely on methanol as a carbon source remains challenging. Here, we apply flux balance analysis to comprehensively identify methanol-dependent strains with high potential for adaptive laboratory evolution. We further investigate two out of 1200 candidate strains, one with a deletion of fructose-1,6-bisphosphatase (fbp) and another with triosephosphate isomerase (tpiA) deleted. In contrast to previous reported methanol-dependent strains, both feature a complete RuMP cycle and incorporate methanol to a high degree, with up to 31 and 99% fractional incorporation into RuMP cycle metabolites. These strains represent ideal starting points for evolution towards a fully methylotrophic lifestyle. Nature Publishing Group UK 2020-10-26 /pmc/articles/PMC7588473/ /pubmed/33106470 http://dx.doi.org/10.1038/s41467-020-19235-5 Text en © The Author(s) 2020 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 Keller, Philipp Noor, Elad Meyer, Fabian Reiter, Michael A. Anastassov, Stanislav Kiefer, Patrick Vorholt, Julia A. Methanol-dependent Escherichia coli strains with a complete ribulose monophosphate cycle |
title | Methanol-dependent Escherichia coli strains with a complete ribulose monophosphate cycle |
title_full | Methanol-dependent Escherichia coli strains with a complete ribulose monophosphate cycle |
title_fullStr | Methanol-dependent Escherichia coli strains with a complete ribulose monophosphate cycle |
title_full_unstemmed | Methanol-dependent Escherichia coli strains with a complete ribulose monophosphate cycle |
title_short | Methanol-dependent Escherichia coli strains with a complete ribulose monophosphate cycle |
title_sort | methanol-dependent escherichia coli strains with a complete ribulose monophosphate cycle |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7588473/ https://www.ncbi.nlm.nih.gov/pubmed/33106470 http://dx.doi.org/10.1038/s41467-020-19235-5 |
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