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Conservation of ethanol fermentation and its regulation in land plants
Ethanol fermentation is considered as one of the main metabolic adaptations to ensure energy production in higher plants under anaerobic conditions. Following this pathway, pyruvate is decarboxylated and reduced to ethanol with the concomitant oxidation of NADH to NAD(+). Despite its acknowledgement...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6436157/ https://www.ncbi.nlm.nih.gov/pubmed/30861072 http://dx.doi.org/10.1093/jxb/erz052 |
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author | Bui, Liem T Novi, Giacomo Lombardi, Lara Iannuzzi, Cristina Rossi, Jacopo Santaniello, Antonietta Mensuali, Anna Corbineau, Françoise Giuntoli, Beatrice Perata, Pierdomenico Zaffagnini, Mirko Licausi, Francesco |
author_facet | Bui, Liem T Novi, Giacomo Lombardi, Lara Iannuzzi, Cristina Rossi, Jacopo Santaniello, Antonietta Mensuali, Anna Corbineau, Françoise Giuntoli, Beatrice Perata, Pierdomenico Zaffagnini, Mirko Licausi, Francesco |
author_sort | Bui, Liem T |
collection | PubMed |
description | Ethanol fermentation is considered as one of the main metabolic adaptations to ensure energy production in higher plants under anaerobic conditions. Following this pathway, pyruvate is decarboxylated and reduced to ethanol with the concomitant oxidation of NADH to NAD(+). Despite its acknowledgement as an essential metabolic strategy, the conservation of this pathway and its regulation throughout plant evolution have not been assessed so far. To address this question, we compared ethanol fermentation in species representing subsequent steps in plant evolution and related it to the structural features and transcriptional regulation of the two enzymes involved: pyruvate decarboxylase (PDC) and alcohol dehydrogenase (ADH). We observed that, despite the conserved ability to produce ethanol upon hypoxia in distant phyla, transcriptional regulation of the enzymes involved is not conserved in ancient plant lineages, whose ADH homologues do not share structural features distinctive for acetaldehyde/ethanol-processing enzymes. Moreover, Arabidopsis mutants devoid of ADH expression exhibited enhanced PDC activity and retained substantial ethanol production under hypoxic conditions. Therefore, we concluded that, whereas ethanol production is a highly conserved adaptation to low oxygen, its catalysis and regulation in land plants probably involve components that will be identified in the future. |
format | Online Article Text |
id | pubmed-6436157 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-64361572019-04-01 Conservation of ethanol fermentation and its regulation in land plants Bui, Liem T Novi, Giacomo Lombardi, Lara Iannuzzi, Cristina Rossi, Jacopo Santaniello, Antonietta Mensuali, Anna Corbineau, Françoise Giuntoli, Beatrice Perata, Pierdomenico Zaffagnini, Mirko Licausi, Francesco J Exp Bot Research Papers Ethanol fermentation is considered as one of the main metabolic adaptations to ensure energy production in higher plants under anaerobic conditions. Following this pathway, pyruvate is decarboxylated and reduced to ethanol with the concomitant oxidation of NADH to NAD(+). Despite its acknowledgement as an essential metabolic strategy, the conservation of this pathway and its regulation throughout plant evolution have not been assessed so far. To address this question, we compared ethanol fermentation in species representing subsequent steps in plant evolution and related it to the structural features and transcriptional regulation of the two enzymes involved: pyruvate decarboxylase (PDC) and alcohol dehydrogenase (ADH). We observed that, despite the conserved ability to produce ethanol upon hypoxia in distant phyla, transcriptional regulation of the enzymes involved is not conserved in ancient plant lineages, whose ADH homologues do not share structural features distinctive for acetaldehyde/ethanol-processing enzymes. Moreover, Arabidopsis mutants devoid of ADH expression exhibited enhanced PDC activity and retained substantial ethanol production under hypoxic conditions. Therefore, we concluded that, whereas ethanol production is a highly conserved adaptation to low oxygen, its catalysis and regulation in land plants probably involve components that will be identified in the future. Oxford University Press 2019-03-01 2019-02-28 /pmc/articles/PMC6436157/ /pubmed/30861072 http://dx.doi.org/10.1093/jxb/erz052 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the Society for Experimental Biology. All rights reserved. For permissions, please email: journals.permissions@oup.com http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Papers Bui, Liem T Novi, Giacomo Lombardi, Lara Iannuzzi, Cristina Rossi, Jacopo Santaniello, Antonietta Mensuali, Anna Corbineau, Françoise Giuntoli, Beatrice Perata, Pierdomenico Zaffagnini, Mirko Licausi, Francesco Conservation of ethanol fermentation and its regulation in land plants |
title | Conservation of ethanol fermentation and its regulation in land plants |
title_full | Conservation of ethanol fermentation and its regulation in land plants |
title_fullStr | Conservation of ethanol fermentation and its regulation in land plants |
title_full_unstemmed | Conservation of ethanol fermentation and its regulation in land plants |
title_short | Conservation of ethanol fermentation and its regulation in land plants |
title_sort | conservation of ethanol fermentation and its regulation in land plants |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6436157/ https://www.ncbi.nlm.nih.gov/pubmed/30861072 http://dx.doi.org/10.1093/jxb/erz052 |
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