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Role of Dissimilative Pathway of Komagataella phaffii (Pichia pastoris): Formaldehyde Toxicity and Energy Metabolism

Komagataella phaffii (aka Pichia pastoris) is a yeast able to grow in methanol as the sole carbon and energy source. This substrate is converted into formaldehyde, a toxic intermediary that can either be assimilated to biomass or dissimilated to CO(2) through the enzymes formaldehyde dehydrogenase (...

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Autores principales: Berrios, Julio, Theron, Chrispian W., Steels, Sébastien, Ponce, Belén, Velastegui, Edgar, Bustos, Cristina, Altamirano, Claudia, Fickers, Patrick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9321669/
https://www.ncbi.nlm.nih.gov/pubmed/35889185
http://dx.doi.org/10.3390/microorganisms10071466
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author Berrios, Julio
Theron, Chrispian W.
Steels, Sébastien
Ponce, Belén
Velastegui, Edgar
Bustos, Cristina
Altamirano, Claudia
Fickers, Patrick
author_facet Berrios, Julio
Theron, Chrispian W.
Steels, Sébastien
Ponce, Belén
Velastegui, Edgar
Bustos, Cristina
Altamirano, Claudia
Fickers, Patrick
author_sort Berrios, Julio
collection PubMed
description Komagataella phaffii (aka Pichia pastoris) is a yeast able to grow in methanol as the sole carbon and energy source. This substrate is converted into formaldehyde, a toxic intermediary that can either be assimilated to biomass or dissimilated to CO(2) through the enzymes formaldehyde dehydrogenase (FLD) and formate dehydrogenase, also producing energy in the form of NADH. The dissimilative pathway has been described as an energy producing and a detoxifying route, but conclusive evidence has not been provided for this. In order to elucidate this theory, we generated mutants lacking the FLD activity (Δfld1) and used flux analysis to evaluate the metabolic impact of this disrupted pathway. Unexpectedly, we found that the specific growth rate of the Δfld1 strain was only slightly lower (92%) than the control. In contrast, the sensitivity to formaldehyde pulses (up to 8mM) was significantly higher in the Δfld1 mutant strain and was associated with a higher maintenance energy. In addition, the intracellular flux estimation revealed a high metabolic flexibility of K. phaffii in response to the disrupted pathway. Our results suggest that the role of the dissimilative pathway is mainly to protect the cells from the harmful effect of formaldehyde, as they were able to compensate for the energy provided from this pathway when disrupted.
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spelling pubmed-93216692022-07-27 Role of Dissimilative Pathway of Komagataella phaffii (Pichia pastoris): Formaldehyde Toxicity and Energy Metabolism Berrios, Julio Theron, Chrispian W. Steels, Sébastien Ponce, Belén Velastegui, Edgar Bustos, Cristina Altamirano, Claudia Fickers, Patrick Microorganisms Article Komagataella phaffii (aka Pichia pastoris) is a yeast able to grow in methanol as the sole carbon and energy source. This substrate is converted into formaldehyde, a toxic intermediary that can either be assimilated to biomass or dissimilated to CO(2) through the enzymes formaldehyde dehydrogenase (FLD) and formate dehydrogenase, also producing energy in the form of NADH. The dissimilative pathway has been described as an energy producing and a detoxifying route, but conclusive evidence has not been provided for this. In order to elucidate this theory, we generated mutants lacking the FLD activity (Δfld1) and used flux analysis to evaluate the metabolic impact of this disrupted pathway. Unexpectedly, we found that the specific growth rate of the Δfld1 strain was only slightly lower (92%) than the control. In contrast, the sensitivity to formaldehyde pulses (up to 8mM) was significantly higher in the Δfld1 mutant strain and was associated with a higher maintenance energy. In addition, the intracellular flux estimation revealed a high metabolic flexibility of K. phaffii in response to the disrupted pathway. Our results suggest that the role of the dissimilative pathway is mainly to protect the cells from the harmful effect of formaldehyde, as they were able to compensate for the energy provided from this pathway when disrupted. MDPI 2022-07-20 /pmc/articles/PMC9321669/ /pubmed/35889185 http://dx.doi.org/10.3390/microorganisms10071466 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Berrios, Julio
Theron, Chrispian W.
Steels, Sébastien
Ponce, Belén
Velastegui, Edgar
Bustos, Cristina
Altamirano, Claudia
Fickers, Patrick
Role of Dissimilative Pathway of Komagataella phaffii (Pichia pastoris): Formaldehyde Toxicity and Energy Metabolism
title Role of Dissimilative Pathway of Komagataella phaffii (Pichia pastoris): Formaldehyde Toxicity and Energy Metabolism
title_full Role of Dissimilative Pathway of Komagataella phaffii (Pichia pastoris): Formaldehyde Toxicity and Energy Metabolism
title_fullStr Role of Dissimilative Pathway of Komagataella phaffii (Pichia pastoris): Formaldehyde Toxicity and Energy Metabolism
title_full_unstemmed Role of Dissimilative Pathway of Komagataella phaffii (Pichia pastoris): Formaldehyde Toxicity and Energy Metabolism
title_short Role of Dissimilative Pathway of Komagataella phaffii (Pichia pastoris): Formaldehyde Toxicity and Energy Metabolism
title_sort role of dissimilative pathway of komagataella phaffii (pichia pastoris): formaldehyde toxicity and energy metabolism
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9321669/
https://www.ncbi.nlm.nih.gov/pubmed/35889185
http://dx.doi.org/10.3390/microorganisms10071466
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