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The apiosyltransferase celery UGT94AX1 catalyzes the biosynthesis of the flavone glycoside apiin

Apiose is a unique branched-chain pentose found in plant glycosides and a key component of the cell wall polysaccharide pectin and other specialized metabolites. More than 1,200 plant-specialized metabolites contain apiose residues, represented by apiin, a distinctive flavone glycoside found in cele...

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Autores principales: Yamashita, Maho, Fujimori, Tae, An, Song, Iguchi, Sho, Takenaka, Yuto, Kajiura, Hiroyuki, Yoshizawa, Takuya, Matsumura, Hiroyoshi, Kobayashi, Masaru, Ono, Eiichiro, Ishimizu, Takeshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10602602/
https://www.ncbi.nlm.nih.gov/pubmed/37433052
http://dx.doi.org/10.1093/plphys/kiad402
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author Yamashita, Maho
Fujimori, Tae
An, Song
Iguchi, Sho
Takenaka, Yuto
Kajiura, Hiroyuki
Yoshizawa, Takuya
Matsumura, Hiroyoshi
Kobayashi, Masaru
Ono, Eiichiro
Ishimizu, Takeshi
author_facet Yamashita, Maho
Fujimori, Tae
An, Song
Iguchi, Sho
Takenaka, Yuto
Kajiura, Hiroyuki
Yoshizawa, Takuya
Matsumura, Hiroyoshi
Kobayashi, Masaru
Ono, Eiichiro
Ishimizu, Takeshi
author_sort Yamashita, Maho
collection PubMed
description Apiose is a unique branched-chain pentose found in plant glycosides and a key component of the cell wall polysaccharide pectin and other specialized metabolites. More than 1,200 plant-specialized metabolites contain apiose residues, represented by apiin, a distinctive flavone glycoside found in celery (Apium graveolens) and parsley (Petroselinum crispum) in the family Apiaceae. The physiological functions of apiin remain obscure, partly due to our lack of knowledge on apiosyltransferase during apiin biosynthesis. Here, we identified UGT94AX1 as an A. graveolens apiosyltransferase (AgApiT) responsible for catalyzing the last sugar modification step in apiin biosynthesis. AgApiT showed strict substrate specificity for the sugar donor, UDP-apiose, and moderate specificity for acceptor substrates, thereby producing various apiose-containing flavone glycosides in celery. Homology modeling of AgApiT with UDP-apiose, followed by site-directed mutagenesis experiments, identified unique Ile139, Phe140, and Leu356 residues in AgApiT, which are seemingly crucial for the recognition of UDP-apiose in the sugar donor pocket. Sequence comparison and molecular phylogenetic analysis of celery glycosyltransferases suggested that AgApiT is the sole apiosyltransferase-encoding gene in the celery genome. Identification of this plant apiosyltransferase gene will enhance our understanding of the physioecological functions of apiose and apiose-containing compounds.
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spelling pubmed-106026022023-10-27 The apiosyltransferase celery UGT94AX1 catalyzes the biosynthesis of the flavone glycoside apiin Yamashita, Maho Fujimori, Tae An, Song Iguchi, Sho Takenaka, Yuto Kajiura, Hiroyuki Yoshizawa, Takuya Matsumura, Hiroyoshi Kobayashi, Masaru Ono, Eiichiro Ishimizu, Takeshi Plant Physiol Research Article Apiose is a unique branched-chain pentose found in plant glycosides and a key component of the cell wall polysaccharide pectin and other specialized metabolites. More than 1,200 plant-specialized metabolites contain apiose residues, represented by apiin, a distinctive flavone glycoside found in celery (Apium graveolens) and parsley (Petroselinum crispum) in the family Apiaceae. The physiological functions of apiin remain obscure, partly due to our lack of knowledge on apiosyltransferase during apiin biosynthesis. Here, we identified UGT94AX1 as an A. graveolens apiosyltransferase (AgApiT) responsible for catalyzing the last sugar modification step in apiin biosynthesis. AgApiT showed strict substrate specificity for the sugar donor, UDP-apiose, and moderate specificity for acceptor substrates, thereby producing various apiose-containing flavone glycosides in celery. Homology modeling of AgApiT with UDP-apiose, followed by site-directed mutagenesis experiments, identified unique Ile139, Phe140, and Leu356 residues in AgApiT, which are seemingly crucial for the recognition of UDP-apiose in the sugar donor pocket. Sequence comparison and molecular phylogenetic analysis of celery glycosyltransferases suggested that AgApiT is the sole apiosyltransferase-encoding gene in the celery genome. Identification of this plant apiosyltransferase gene will enhance our understanding of the physioecological functions of apiose and apiose-containing compounds. Oxford University Press 2023-07-11 /pmc/articles/PMC10602602/ /pubmed/37433052 http://dx.doi.org/10.1093/plphys/kiad402 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of American Society of Plant Biologists. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://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 Article
Yamashita, Maho
Fujimori, Tae
An, Song
Iguchi, Sho
Takenaka, Yuto
Kajiura, Hiroyuki
Yoshizawa, Takuya
Matsumura, Hiroyoshi
Kobayashi, Masaru
Ono, Eiichiro
Ishimizu, Takeshi
The apiosyltransferase celery UGT94AX1 catalyzes the biosynthesis of the flavone glycoside apiin
title The apiosyltransferase celery UGT94AX1 catalyzes the biosynthesis of the flavone glycoside apiin
title_full The apiosyltransferase celery UGT94AX1 catalyzes the biosynthesis of the flavone glycoside apiin
title_fullStr The apiosyltransferase celery UGT94AX1 catalyzes the biosynthesis of the flavone glycoside apiin
title_full_unstemmed The apiosyltransferase celery UGT94AX1 catalyzes the biosynthesis of the flavone glycoside apiin
title_short The apiosyltransferase celery UGT94AX1 catalyzes the biosynthesis of the flavone glycoside apiin
title_sort apiosyltransferase celery ugt94ax1 catalyzes the biosynthesis of the flavone glycoside apiin
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10602602/
https://www.ncbi.nlm.nih.gov/pubmed/37433052
http://dx.doi.org/10.1093/plphys/kiad402
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