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Conversion of carlactone to carlactonoic acid is a conserved function of MAX1 homologs in strigolactone biosynthesis.

Identifieur interne : 000F78 ( Main/Exploration ); précédent : 000F77; suivant : 000F79

Conversion of carlactone to carlactonoic acid is a conserved function of MAX1 homologs in strigolactone biosynthesis.

Auteurs : Kaori Yoneyama [Japon] ; Narumi Mori [Japon] ; Tomoyasu Sato [Japon] ; Akiyoshi Yoda [Japon] ; Xiaonan Xie [Japon] ; Masanori Okamoto [Japon] ; Masashi Iwanaga [Japon] ; Toshiyuki Ohnishi [Japon] ; Hisashi Nishiwaki [Japon] ; Tadao Asami [Japon] ; Takao Yokota [Japon] ; Kohki Akiyama [Japon] ; Koichi Yoneyama [Japon] ; Takahito Nomura [Japon]

Source :

RBID : pubmed:29479714

Descripteurs français

English descriptors

Abstract

Strigolactones (SLs) are a class of plant hormones which regulate shoot branching and function as host recognition signals for symbionts and parasites in the rhizosphere. However, steps in SL biosynthesis after carlactone (CL) formation remain elusive. This study elucidated the common and diverse functions of MAX1 homologs which catalyze CL oxidation. We have reported previously that ArabidopsisMAX1 converts CL to carlactonoic acid (CLA), whereas a rice MAX1 homolog has been shown to catalyze the conversion of CL to 4-deoxyorobanchol (4DO). To determine which reaction is conserved in the plant kingdom, we investigated the enzymatic function of MAX1 homologs in Arabidopsis, rice, maize, tomato, poplar and Selaginella moellendorffii. The conversion of CL to CLA was found to be a common reaction catalyzed by MAX1 homologs, and MAX1s can be classified into three types: A1-type, converting CL to CLA; A2-type, converting CL to 4DO via CLA; and A3-type, converting CL to CLA and 4DO to orobanchol. CLA was detected in root exudates from poplar and Selaginella, but not ubiquitously in other plants examined in this study, suggesting its role as a species-specific signal in the rhizosphere. This study provides new insights into the roles of MAX1 in endogenous and rhizosphere signaling.

DOI: 10.1111/nph.15055
PubMed: 29479714


Affiliations:


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Le document en format XML

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<name sortKey="Okamoto, Masanori" sort="Okamoto, Masanori" uniqKey="Okamoto M" first="Masanori" last="Okamoto">Masanori Okamoto</name>
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<name sortKey="Iwanaga, Masashi" sort="Iwanaga, Masashi" uniqKey="Iwanaga M" first="Masashi" last="Iwanaga">Masashi Iwanaga</name>
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<name sortKey="Yoneyama, Koichi" sort="Yoneyama, Koichi" uniqKey="Yoneyama K" first="Koichi" last="Yoneyama">Koichi Yoneyama</name>
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<name sortKey="Nomura, Takahito" sort="Nomura, Takahito" uniqKey="Nomura T" first="Takahito" last="Nomura">Takahito Nomura</name>
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<name sortKey="Sato, Tomoyasu" sort="Sato, Tomoyasu" uniqKey="Sato T" first="Tomoyasu" last="Sato">Tomoyasu Sato</name>
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<name sortKey="Akiyama, Kohki" sort="Akiyama, Kohki" uniqKey="Akiyama K" first="Kohki" last="Akiyama">Kohki Akiyama</name>
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<nlm:affiliation>Department of Applied Life Sciences, Graduate School of Life and Environmental Sciences, Osaka Prefecture University, Sakai, Osaka, 599-8531, Japan.</nlm:affiliation>
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<wicri:regionArea>Department of Applied Life Sciences, Graduate School of Life and Environmental Sciences, Osaka Prefecture University, Sakai, Osaka, 599-8531</wicri:regionArea>
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<name sortKey="Yoneyama, Koichi" sort="Yoneyama, Koichi" uniqKey="Yoneyama K" first="Koichi" last="Yoneyama">Koichi Yoneyama</name>
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<country xml:lang="fr">Japon</country>
<wicri:regionArea>Center for Bioscience Research and Education, Utsunomiya University, Utsunomiya, 321-8505</wicri:regionArea>
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<name sortKey="Nomura, Takahito" sort="Nomura, Takahito" uniqKey="Nomura T" first="Takahito" last="Nomura">Takahito Nomura</name>
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<term>Lactones (metabolism)</term>
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<term>Microsomes (metabolism)</term>
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<term>Plant Growth Regulators (metabolism)</term>
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<term>Facteur de croissance végétal (métabolisme)</term>
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<div type="abstract" xml:lang="en">Strigolactones (SLs) are a class of plant hormones which regulate shoot branching and function as host recognition signals for symbionts and parasites in the rhizosphere. However, steps in SL biosynthesis after carlactone (CL) formation remain elusive. This study elucidated the common and diverse functions of MAX1 homologs which catalyze CL oxidation. We have reported previously that ArabidopsisMAX1 converts CL to carlactonoic acid (CLA), whereas a rice MAX1 homolog has been shown to catalyze the conversion of CL to 4-deoxyorobanchol (4DO). To determine which reaction is conserved in the plant kingdom, we investigated the enzymatic function of MAX1 homologs in Arabidopsis, rice, maize, tomato, poplar and Selaginella moellendorffii. The conversion of CL to CLA was found to be a common reaction catalyzed by MAX1 homologs, and MAX1s can be classified into three types: A1-type, converting CL to CLA; A2-type, converting CL to 4DO via CLA; and A3-type, converting CL to CLA and 4DO to orobanchol. CLA was detected in root exudates from poplar and Selaginella, but not ubiquitously in other plants examined in this study, suggesting its role as a species-specific signal in the rhizosphere. This study provides new insights into the roles of MAX1 in endogenous and rhizosphere signaling.</div>
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<Day>30</Day>
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<AbstractText>Strigolactones (SLs) are a class of plant hormones which regulate shoot branching and function as host recognition signals for symbionts and parasites in the rhizosphere. However, steps in SL biosynthesis after carlactone (CL) formation remain elusive. This study elucidated the common and diverse functions of MAX1 homologs which catalyze CL oxidation. We have reported previously that ArabidopsisMAX1 converts CL to carlactonoic acid (CLA), whereas a rice MAX1 homolog has been shown to catalyze the conversion of CL to 4-deoxyorobanchol (4DO). To determine which reaction is conserved in the plant kingdom, we investigated the enzymatic function of MAX1 homologs in Arabidopsis, rice, maize, tomato, poplar and Selaginella moellendorffii. The conversion of CL to CLA was found to be a common reaction catalyzed by MAX1 homologs, and MAX1s can be classified into three types: A1-type, converting CL to CLA; A2-type, converting CL to 4DO via CLA; and A3-type, converting CL to CLA and 4DO to orobanchol. CLA was detected in root exudates from poplar and Selaginella, but not ubiquitously in other plants examined in this study, suggesting its role as a species-specific signal in the rhizosphere. This study provides new insights into the roles of MAX1 in endogenous and rhizosphere signaling.</AbstractText>
<CopyrightInformation>© 2018 The Authors. New Phytologist © 2018 New Phytologist Trust.</CopyrightInformation>
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<AffiliationInfo>
<Affiliation>Graduate School of Agriculture, Ehime University, Ehime, 790-8566, Japan.</Affiliation>
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