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The oxygen-tolerant reductive glycine pathway assimilates methanol, formate and CO(2) in the yeast Komagataella phaffii

The current climatic change is predominantly driven by excessive anthropogenic CO(2) emissions. As industrial bioprocesses primarily depend on food-competing organic feedstocks or fossil raw materials, CO(2) co-assimilation or the use of CO(2)-derived methanol or formate as carbon sources are consid...

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Autores principales: Mitic, Bernd M., Troyer, Christina, Lutz, Lisa, Baumschabl, Michael, Hann, Stephan, Mattanovich, Diethard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10682033/
https://www.ncbi.nlm.nih.gov/pubmed/38012236
http://dx.doi.org/10.1038/s41467-023-43610-7
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author Mitic, Bernd M.
Troyer, Christina
Lutz, Lisa
Baumschabl, Michael
Hann, Stephan
Mattanovich, Diethard
author_facet Mitic, Bernd M.
Troyer, Christina
Lutz, Lisa
Baumschabl, Michael
Hann, Stephan
Mattanovich, Diethard
author_sort Mitic, Bernd M.
collection PubMed
description The current climatic change is predominantly driven by excessive anthropogenic CO(2) emissions. As industrial bioprocesses primarily depend on food-competing organic feedstocks or fossil raw materials, CO(2) co-assimilation or the use of CO(2)-derived methanol or formate as carbon sources are considered pathbreaking contributions to solving this global problem. The number of industrially-relevant microorganisms that can use these two carbon sources is limited, and even fewer can concurrently co-assimilate CO(2). Here, we search for alternative native methanol and formate assimilation pathways that co-assimilate CO(2) in the industrially-relevant methylotrophic yeast Komagataella phaffii (Pichia pastoris). Using (13)C-tracer-based metabolomic techniques and metabolic engineering approaches, we discover and confirm a growth supporting pathway based on native enzymes that can perform all three assimilations: namely, the oxygen-tolerant reductive glycine pathway. This finding paves the way towards metabolic engineering of formate and CO(2) utilisation to produce proteins, biomass, or chemicals in yeast.
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spelling pubmed-106820332023-11-30 The oxygen-tolerant reductive glycine pathway assimilates methanol, formate and CO(2) in the yeast Komagataella phaffii Mitic, Bernd M. Troyer, Christina Lutz, Lisa Baumschabl, Michael Hann, Stephan Mattanovich, Diethard Nat Commun Article The current climatic change is predominantly driven by excessive anthropogenic CO(2) emissions. As industrial bioprocesses primarily depend on food-competing organic feedstocks or fossil raw materials, CO(2) co-assimilation or the use of CO(2)-derived methanol or formate as carbon sources are considered pathbreaking contributions to solving this global problem. The number of industrially-relevant microorganisms that can use these two carbon sources is limited, and even fewer can concurrently co-assimilate CO(2). Here, we search for alternative native methanol and formate assimilation pathways that co-assimilate CO(2) in the industrially-relevant methylotrophic yeast Komagataella phaffii (Pichia pastoris). Using (13)C-tracer-based metabolomic techniques and metabolic engineering approaches, we discover and confirm a growth supporting pathway based on native enzymes that can perform all three assimilations: namely, the oxygen-tolerant reductive glycine pathway. This finding paves the way towards metabolic engineering of formate and CO(2) utilisation to produce proteins, biomass, or chemicals in yeast. Nature Publishing Group UK 2023-11-27 /pmc/articles/PMC10682033/ /pubmed/38012236 http://dx.doi.org/10.1038/s41467-023-43610-7 Text en © The Author(s) 2023 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Mitic, Bernd M.
Troyer, Christina
Lutz, Lisa
Baumschabl, Michael
Hann, Stephan
Mattanovich, Diethard
The oxygen-tolerant reductive glycine pathway assimilates methanol, formate and CO(2) in the yeast Komagataella phaffii
title The oxygen-tolerant reductive glycine pathway assimilates methanol, formate and CO(2) in the yeast Komagataella phaffii
title_full The oxygen-tolerant reductive glycine pathway assimilates methanol, formate and CO(2) in the yeast Komagataella phaffii
title_fullStr The oxygen-tolerant reductive glycine pathway assimilates methanol, formate and CO(2) in the yeast Komagataella phaffii
title_full_unstemmed The oxygen-tolerant reductive glycine pathway assimilates methanol, formate and CO(2) in the yeast Komagataella phaffii
title_short The oxygen-tolerant reductive glycine pathway assimilates methanol, formate and CO(2) in the yeast Komagataella phaffii
title_sort oxygen-tolerant reductive glycine pathway assimilates methanol, formate and co(2) in the yeast komagataella phaffii
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10682033/
https://www.ncbi.nlm.nih.gov/pubmed/38012236
http://dx.doi.org/10.1038/s41467-023-43610-7
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