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NADH-GOGAT Overexpression Does Not Improve Maize (Zea mays L.) Performance Even When Pyramiding with NAD-IDH, GDH and GS

Maize plants overexpressing NADH-GOGAT were produced in order to determine if boosting 2-Oxoglurate production used as a carbon skeleton for the biosynthesis of amino acids will improve plant biomass and kernel production. The NADH-GOGAT enzyme recycles glutamate and incorporates carbon skeletons in...

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Autores principales: Cañas, Rafael A., Yesbergenova-Cuny, Zhazira, Belanger, Léo, Rouster, Jacques, Brulé, Lenaïg, Gilard, Françoise, Quilleré, Isabelle, Sallaud, Christophe, Hirel, Bertrand
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7076717/
https://www.ncbi.nlm.nih.gov/pubmed/31973049
http://dx.doi.org/10.3390/plants9020130
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author Cañas, Rafael A.
Yesbergenova-Cuny, Zhazira
Belanger, Léo
Rouster, Jacques
Brulé, Lenaïg
Gilard, Françoise
Quilleré, Isabelle
Sallaud, Christophe
Hirel, Bertrand
author_facet Cañas, Rafael A.
Yesbergenova-Cuny, Zhazira
Belanger, Léo
Rouster, Jacques
Brulé, Lenaïg
Gilard, Françoise
Quilleré, Isabelle
Sallaud, Christophe
Hirel, Bertrand
author_sort Cañas, Rafael A.
collection PubMed
description Maize plants overexpressing NADH-GOGAT were produced in order to determine if boosting 2-Oxoglurate production used as a carbon skeleton for the biosynthesis of amino acids will improve plant biomass and kernel production. The NADH-GOGAT enzyme recycles glutamate and incorporates carbon skeletons into the ammonium assimilation pathway using the organic acid 2-Oxoglutarate as a substrate. Gene pyramiding was then conducted with NAD-IDH and NADH-GDH, two enzymes also involved in the synthesis of 2-Oxoglurate. NADH-GOGAT overexpression was detrimental for shoot biomass production but did not markedly affect kernel yield. Additional NAD-IDH and NADH-GDH activity did not improve plant performance. A decrease in kernel production was observed when NADH-GDH was pyramided to NADH-GOGAT and NAD-IDH. This decrease could not be restored even when additional cytosolic GS activity was present in the plants overexpressing the three enzymes producing 2-Oxoglutarate. Detailed leaf metabolic profiling of the different transgenic plants revealed that the NADH-GOGAT over-expressors were characterized by an accumulation of amino acids derived from glutamate and a decrease in the amount of carbohydrates further used to provide carbon skeletons for its synthesis. The study suggests that 2-Oxoglutarate synthesis is a key element acting at the interface of carbohydrate and amino acid metabolism and that its accumulation induces an imbalance of primary carbon and nitrogen metabolism that is detrimental for maize productivity.
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spelling pubmed-70767172020-03-20 NADH-GOGAT Overexpression Does Not Improve Maize (Zea mays L.) Performance Even When Pyramiding with NAD-IDH, GDH and GS Cañas, Rafael A. Yesbergenova-Cuny, Zhazira Belanger, Léo Rouster, Jacques Brulé, Lenaïg Gilard, Françoise Quilleré, Isabelle Sallaud, Christophe Hirel, Bertrand Plants (Basel) Article Maize plants overexpressing NADH-GOGAT were produced in order to determine if boosting 2-Oxoglurate production used as a carbon skeleton for the biosynthesis of amino acids will improve plant biomass and kernel production. The NADH-GOGAT enzyme recycles glutamate and incorporates carbon skeletons into the ammonium assimilation pathway using the organic acid 2-Oxoglutarate as a substrate. Gene pyramiding was then conducted with NAD-IDH and NADH-GDH, two enzymes also involved in the synthesis of 2-Oxoglurate. NADH-GOGAT overexpression was detrimental for shoot biomass production but did not markedly affect kernel yield. Additional NAD-IDH and NADH-GDH activity did not improve plant performance. A decrease in kernel production was observed when NADH-GDH was pyramided to NADH-GOGAT and NAD-IDH. This decrease could not be restored even when additional cytosolic GS activity was present in the plants overexpressing the three enzymes producing 2-Oxoglutarate. Detailed leaf metabolic profiling of the different transgenic plants revealed that the NADH-GOGAT over-expressors were characterized by an accumulation of amino acids derived from glutamate and a decrease in the amount of carbohydrates further used to provide carbon skeletons for its synthesis. The study suggests that 2-Oxoglutarate synthesis is a key element acting at the interface of carbohydrate and amino acid metabolism and that its accumulation induces an imbalance of primary carbon and nitrogen metabolism that is detrimental for maize productivity. MDPI 2020-01-21 /pmc/articles/PMC7076717/ /pubmed/31973049 http://dx.doi.org/10.3390/plants9020130 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Cañas, Rafael A.
Yesbergenova-Cuny, Zhazira
Belanger, Léo
Rouster, Jacques
Brulé, Lenaïg
Gilard, Françoise
Quilleré, Isabelle
Sallaud, Christophe
Hirel, Bertrand
NADH-GOGAT Overexpression Does Not Improve Maize (Zea mays L.) Performance Even When Pyramiding with NAD-IDH, GDH and GS
title NADH-GOGAT Overexpression Does Not Improve Maize (Zea mays L.) Performance Even When Pyramiding with NAD-IDH, GDH and GS
title_full NADH-GOGAT Overexpression Does Not Improve Maize (Zea mays L.) Performance Even When Pyramiding with NAD-IDH, GDH and GS
title_fullStr NADH-GOGAT Overexpression Does Not Improve Maize (Zea mays L.) Performance Even When Pyramiding with NAD-IDH, GDH and GS
title_full_unstemmed NADH-GOGAT Overexpression Does Not Improve Maize (Zea mays L.) Performance Even When Pyramiding with NAD-IDH, GDH and GS
title_short NADH-GOGAT Overexpression Does Not Improve Maize (Zea mays L.) Performance Even When Pyramiding with NAD-IDH, GDH and GS
title_sort nadh-gogat overexpression does not improve maize (zea mays l.) performance even when pyramiding with nad-idh, gdh and gs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7076717/
https://www.ncbi.nlm.nih.gov/pubmed/31973049
http://dx.doi.org/10.3390/plants9020130
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