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Characterization of Four Bifunctional Plant IAM/PAM-Amidohydrolases Capable of Contributing to Auxin Biosynthesis

Amidases [EC 3.5.1.4] capable of converting indole-3-acetamide (IAM) into the major plant growth hormone indole-3-acetic acid (IAA) are assumed to be involved in auxin de novo biosynthesis. With the emerging amount of genomics data, it was possible to identify over forty proteins with substantial ho...

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Autores principales: Sánchez-Parra, Beatriz, Frerigmann, Henning, Pérez Alonso, Marta-Marina, Carrasco Loba, Víctor, Jost, Ricarda, Hentrich, Mathias, Pollmann, Stephan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4844348/
https://www.ncbi.nlm.nih.gov/pubmed/27135507
http://dx.doi.org/10.3390/plants3030324
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author Sánchez-Parra, Beatriz
Frerigmann, Henning
Pérez Alonso, Marta-Marina
Carrasco Loba, Víctor
Jost, Ricarda
Hentrich, Mathias
Pollmann, Stephan
author_facet Sánchez-Parra, Beatriz
Frerigmann, Henning
Pérez Alonso, Marta-Marina
Carrasco Loba, Víctor
Jost, Ricarda
Hentrich, Mathias
Pollmann, Stephan
author_sort Sánchez-Parra, Beatriz
collection PubMed
description Amidases [EC 3.5.1.4] capable of converting indole-3-acetamide (IAM) into the major plant growth hormone indole-3-acetic acid (IAA) are assumed to be involved in auxin de novo biosynthesis. With the emerging amount of genomics data, it was possible to identify over forty proteins with substantial homology to the already characterized amidases from Arabidopsis and tobacco. The observed high conservation of amidase-like proteins throughout the plant kingdom may suggest an important role of theses enzymes in plant development. Here, we report cloning and functional analysis of four, thus far, uncharacterized plant amidases from Oryza sativa, Sorghum bicolor, Medicago truncatula, and Populus trichocarpa. Intriguingly, we were able to demonstrate that the examined amidases are also capable of converting phenyl-2-acetamide (PAM) into phenyl-2-acetic acid (PAA), an auxin endogenous to several plant species including Arabidopsis. Furthermore, we compared the subcellular localization of the enzymes to that of Arabidopsis AMI1, providing further evidence for similar enzymatic functions. Our results point to the presence of a presumably conserved pathway of auxin biosynthesis via IAM, as amidases, both of monocot, and dicot origins, were analyzed.
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spelling pubmed-48443482016-04-29 Characterization of Four Bifunctional Plant IAM/PAM-Amidohydrolases Capable of Contributing to Auxin Biosynthesis Sánchez-Parra, Beatriz Frerigmann, Henning Pérez Alonso, Marta-Marina Carrasco Loba, Víctor Jost, Ricarda Hentrich, Mathias Pollmann, Stephan Plants (Basel) Article Amidases [EC 3.5.1.4] capable of converting indole-3-acetamide (IAM) into the major plant growth hormone indole-3-acetic acid (IAA) are assumed to be involved in auxin de novo biosynthesis. With the emerging amount of genomics data, it was possible to identify over forty proteins with substantial homology to the already characterized amidases from Arabidopsis and tobacco. The observed high conservation of amidase-like proteins throughout the plant kingdom may suggest an important role of theses enzymes in plant development. Here, we report cloning and functional analysis of four, thus far, uncharacterized plant amidases from Oryza sativa, Sorghum bicolor, Medicago truncatula, and Populus trichocarpa. Intriguingly, we were able to demonstrate that the examined amidases are also capable of converting phenyl-2-acetamide (PAM) into phenyl-2-acetic acid (PAA), an auxin endogenous to several plant species including Arabidopsis. Furthermore, we compared the subcellular localization of the enzymes to that of Arabidopsis AMI1, providing further evidence for similar enzymatic functions. Our results point to the presence of a presumably conserved pathway of auxin biosynthesis via IAM, as amidases, both of monocot, and dicot origins, were analyzed. MDPI 2014-08-07 /pmc/articles/PMC4844348/ /pubmed/27135507 http://dx.doi.org/10.3390/plants3030324 Text en © 2014 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 license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Sánchez-Parra, Beatriz
Frerigmann, Henning
Pérez Alonso, Marta-Marina
Carrasco Loba, Víctor
Jost, Ricarda
Hentrich, Mathias
Pollmann, Stephan
Characterization of Four Bifunctional Plant IAM/PAM-Amidohydrolases Capable of Contributing to Auxin Biosynthesis
title Characterization of Four Bifunctional Plant IAM/PAM-Amidohydrolases Capable of Contributing to Auxin Biosynthesis
title_full Characterization of Four Bifunctional Plant IAM/PAM-Amidohydrolases Capable of Contributing to Auxin Biosynthesis
title_fullStr Characterization of Four Bifunctional Plant IAM/PAM-Amidohydrolases Capable of Contributing to Auxin Biosynthesis
title_full_unstemmed Characterization of Four Bifunctional Plant IAM/PAM-Amidohydrolases Capable of Contributing to Auxin Biosynthesis
title_short Characterization of Four Bifunctional Plant IAM/PAM-Amidohydrolases Capable of Contributing to Auxin Biosynthesis
title_sort characterization of four bifunctional plant iam/pam-amidohydrolases capable of contributing to auxin biosynthesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4844348/
https://www.ncbi.nlm.nih.gov/pubmed/27135507
http://dx.doi.org/10.3390/plants3030324
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