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New Insights into rice pyrimidine catabolic enzymes

INTRODUCTION: Rice is a primary global food source, and its production is affected by abiotic stress, caused by climate change and other factors. Recently, the pyrimidine reductive catabolic pathway, catalyzed by dihydropyrimidine dehydrogenase (DHPD), dihydropyrimidinase (DHP) and β-ureidopropionas...

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Autores principales: Lopez, Andrea J., Narvaez-Ortiz, Heidy Y., Rincon-Benavides, Maria A., Pulido, Dania Camila, Fuentes Suarez, Luis Eduardo, Zimmermann, Barbara H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9930899/
https://www.ncbi.nlm.nih.gov/pubmed/36818891
http://dx.doi.org/10.3389/fpls.2023.1079778
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author Lopez, Andrea J.
Narvaez-Ortiz, Heidy Y.
Rincon-Benavides, Maria A.
Pulido, Dania Camila
Fuentes Suarez, Luis Eduardo
Zimmermann, Barbara H.
author_facet Lopez, Andrea J.
Narvaez-Ortiz, Heidy Y.
Rincon-Benavides, Maria A.
Pulido, Dania Camila
Fuentes Suarez, Luis Eduardo
Zimmermann, Barbara H.
author_sort Lopez, Andrea J.
collection PubMed
description INTRODUCTION: Rice is a primary global food source, and its production is affected by abiotic stress, caused by climate change and other factors. Recently, the pyrimidine reductive catabolic pathway, catalyzed by dihydropyrimidine dehydrogenase (DHPD), dihydropyrimidinase (DHP) and β-ureidopropionase (β-UP), has emerged as a potential participant in the abiotic stress response of rice. METHODS: The rice enzymes were produced as recombinant proteins, and two were kinetically characterized. Rice dihydroorotate dehydrogenase (DHODH), an enzyme of pyrimidine biosynthesis often confused with DHPD, was also characterized. Salt-sensitive and salt-resistant rice seedlings were subjected to salt stress (24 h) and metabolites in leaves were determined by mass spectrometry. RESULTS: The OsDHPD sequence was homologous to the C-terminal half of mammalian DHPD, conserving FMN and uracil binding sites, but lacked sites for Fe/S clusters, FAD, and NADPH. OsDHPD, truncated to eliminate the chloroplast targeting peptide, was soluble, but inactive. Database searches for polypeptides homologous to the N-terminal half of mammalian DHPD, that could act as co-reductants, were unsuccessful. OsDHODH exhibited kinetic parameters similar to those of other plant DHODHs. OsDHP, truncated to remove a signal sequence, exhibited a kcat/Km = 3.6 x 103 s-1M-1. Osb-UP exhibited a kcat/Km = 1.8 x 104 s-1M-1. Short-term salt exposure caused insignificant differences in the levels of the ureide intermediates dihydrouracil and ureidopropionate in leaves of salt-sensitive and salt-resistant plants. Allantoin, a ureide metabolite of purine catabolism, was found to be significantly higher in the resistant cultivar compared to one of the sensitive cultivars. DISCUSSION: OsDHP, the first plant enzyme to be characterized, showed low kinetic efficiency, but its activity may have been affected by truncation. Osb-UP exhibited kinetic parameters in the range of enzymes of secondary metabolism. Levels of two pathway metabolites were similar in sensitive and resistant cultivars and appeared to be unaffected by short-term salt exposure.”
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spelling pubmed-99308992023-02-16 New Insights into rice pyrimidine catabolic enzymes Lopez, Andrea J. Narvaez-Ortiz, Heidy Y. Rincon-Benavides, Maria A. Pulido, Dania Camila Fuentes Suarez, Luis Eduardo Zimmermann, Barbara H. Front Plant Sci Plant Science INTRODUCTION: Rice is a primary global food source, and its production is affected by abiotic stress, caused by climate change and other factors. Recently, the pyrimidine reductive catabolic pathway, catalyzed by dihydropyrimidine dehydrogenase (DHPD), dihydropyrimidinase (DHP) and β-ureidopropionase (β-UP), has emerged as a potential participant in the abiotic stress response of rice. METHODS: The rice enzymes were produced as recombinant proteins, and two were kinetically characterized. Rice dihydroorotate dehydrogenase (DHODH), an enzyme of pyrimidine biosynthesis often confused with DHPD, was also characterized. Salt-sensitive and salt-resistant rice seedlings were subjected to salt stress (24 h) and metabolites in leaves were determined by mass spectrometry. RESULTS: The OsDHPD sequence was homologous to the C-terminal half of mammalian DHPD, conserving FMN and uracil binding sites, but lacked sites for Fe/S clusters, FAD, and NADPH. OsDHPD, truncated to eliminate the chloroplast targeting peptide, was soluble, but inactive. Database searches for polypeptides homologous to the N-terminal half of mammalian DHPD, that could act as co-reductants, were unsuccessful. OsDHODH exhibited kinetic parameters similar to those of other plant DHODHs. OsDHP, truncated to remove a signal sequence, exhibited a kcat/Km = 3.6 x 103 s-1M-1. Osb-UP exhibited a kcat/Km = 1.8 x 104 s-1M-1. Short-term salt exposure caused insignificant differences in the levels of the ureide intermediates dihydrouracil and ureidopropionate in leaves of salt-sensitive and salt-resistant plants. Allantoin, a ureide metabolite of purine catabolism, was found to be significantly higher in the resistant cultivar compared to one of the sensitive cultivars. DISCUSSION: OsDHP, the first plant enzyme to be characterized, showed low kinetic efficiency, but its activity may have been affected by truncation. Osb-UP exhibited kinetic parameters in the range of enzymes of secondary metabolism. Levels of two pathway metabolites were similar in sensitive and resistant cultivars and appeared to be unaffected by short-term salt exposure.” Frontiers Media S.A. 2023-02-01 /pmc/articles/PMC9930899/ /pubmed/36818891 http://dx.doi.org/10.3389/fpls.2023.1079778 Text en Copyright © 2023 Lopez, Narvaez-Ortiz, Rincon-Benavides, Pulido, Fuentes Suarez and Zimmermann https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Lopez, Andrea J.
Narvaez-Ortiz, Heidy Y.
Rincon-Benavides, Maria A.
Pulido, Dania Camila
Fuentes Suarez, Luis Eduardo
Zimmermann, Barbara H.
New Insights into rice pyrimidine catabolic enzymes
title New Insights into rice pyrimidine catabolic enzymes
title_full New Insights into rice pyrimidine catabolic enzymes
title_fullStr New Insights into rice pyrimidine catabolic enzymes
title_full_unstemmed New Insights into rice pyrimidine catabolic enzymes
title_short New Insights into rice pyrimidine catabolic enzymes
title_sort new insights into rice pyrimidine catabolic enzymes
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9930899/
https://www.ncbi.nlm.nih.gov/pubmed/36818891
http://dx.doi.org/10.3389/fpls.2023.1079778
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