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 a...

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Veröffentlicht in:Journal of experimental botany 2019-03, Vol.70 (6), p.1815-1827
Hauptverfasser: 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
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container_end_page 1827
container_issue 6
container_start_page 1815
container_title Journal of experimental botany
container_volume 70
creator 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
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 .
doi_str_mv 10.1093/jxb/erz052
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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. 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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 .</abstract><cop>UK</cop><pub>Oxford University Press</pub><pmid>30861072</pmid><doi>10.1093/jxb/erz052</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0001-9444-0610</orcidid><orcidid>https://orcid.org/0000-0003-4769-441X</orcidid><oa>free_for_read</oa></addata></record>
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source Oxford University Press Journals All Titles (1996-Current); MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
subjects acetaldehyde
alcohol dehydrogenase
Alcohol Dehydrogenase - metabolism
anaerobic conditions
Arabidopsis
Biochemistry
Biochemistry, Molecular Biology
Biological Evolution
Botanics
catalytic activity
Embryophyta - enzymology
Embryophyta - metabolism
embryophytes
energy
ethanol
Ethanol - metabolism
ethanol fermentation
ethanol production
evolution
Fermentation
hypoxia
Life Sciences
mutants
NAD (coenzyme)
oxidation
oxygen
Photosynthesis and Metabolism
pyruvate decarboxylase
Pyruvate Decarboxylase - metabolism
pyruvic acid
Research Papers
transcription (genetics)
Vegetal Biology
title Conservation of ethanol fermentation and its regulation in land plants
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