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Triflumizole as a Novel Lead Compound for Strigolactone Biosynthesis Inhibitor

Strigolactones (SLs) are carotenoid-derived plant hormones involved in the development of various plants. SLs also stimulate seed germination of the root parasitic plants, Striga spp. and Orobanche spp., which reduce crop yield. Therefore, regulating SL biosynthesis may lessen the damage of root par...

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Autores principales: Kawada, Kojiro, Uchida, Yuya, Takahashi, Ikuo, Nomura, Takahito, Sasaki, Yasuyuki, Asami, Tadao, Yajima, Shunsuke, Ito, Shinsaku
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7728069/
https://www.ncbi.nlm.nih.gov/pubmed/33255720
http://dx.doi.org/10.3390/molecules25235525
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author Kawada, Kojiro
Uchida, Yuya
Takahashi, Ikuo
Nomura, Takahito
Sasaki, Yasuyuki
Asami, Tadao
Yajima, Shunsuke
Ito, Shinsaku
author_facet Kawada, Kojiro
Uchida, Yuya
Takahashi, Ikuo
Nomura, Takahito
Sasaki, Yasuyuki
Asami, Tadao
Yajima, Shunsuke
Ito, Shinsaku
author_sort Kawada, Kojiro
collection PubMed
description Strigolactones (SLs) are carotenoid-derived plant hormones involved in the development of various plants. SLs also stimulate seed germination of the root parasitic plants, Striga spp. and Orobanche spp., which reduce crop yield. Therefore, regulating SL biosynthesis may lessen the damage of root parasitic plants. Biosynthetic inhibitors effectively control biological processes by targeted regulation of biologically active compounds. In addition, biosynthetic inhibitors regulate endogenous levels in developmental stage- and tissue-specific manners. To date, although some chemicals have been found as SL biosynthesis inhibitor, these are derived from only three lead chemicals. In this study, to find a novel lead chemical for SL biosynthesis inhibitor, 27 nitrogen-containing heterocyclic derivatives were screened for inhibition of SL biosynthesis. Triflumizole most effectively reduced the levels of rice SL, 4-deoxyorobanchol (4DO), in root exudates. In addition, triflumizole inhibited endogenous 4DO biosynthesis in rice roots by inhibiting the enzymatic activity of Os900, a rice enzyme that converts the SL intermediate carlactone to 4DO. A Striga germination assay revealed that triflumizole-treated rice displayed a reduced level of germination stimulation for Striga. These results identify triflumizole as a novel lead compound for inhibition of SL biosynthesis.
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spelling pubmed-77280692020-12-11 Triflumizole as a Novel Lead Compound for Strigolactone Biosynthesis Inhibitor Kawada, Kojiro Uchida, Yuya Takahashi, Ikuo Nomura, Takahito Sasaki, Yasuyuki Asami, Tadao Yajima, Shunsuke Ito, Shinsaku Molecules Article Strigolactones (SLs) are carotenoid-derived plant hormones involved in the development of various plants. SLs also stimulate seed germination of the root parasitic plants, Striga spp. and Orobanche spp., which reduce crop yield. Therefore, regulating SL biosynthesis may lessen the damage of root parasitic plants. Biosynthetic inhibitors effectively control biological processes by targeted regulation of biologically active compounds. In addition, biosynthetic inhibitors regulate endogenous levels in developmental stage- and tissue-specific manners. To date, although some chemicals have been found as SL biosynthesis inhibitor, these are derived from only three lead chemicals. In this study, to find a novel lead chemical for SL biosynthesis inhibitor, 27 nitrogen-containing heterocyclic derivatives were screened for inhibition of SL biosynthesis. Triflumizole most effectively reduced the levels of rice SL, 4-deoxyorobanchol (4DO), in root exudates. In addition, triflumizole inhibited endogenous 4DO biosynthesis in rice roots by inhibiting the enzymatic activity of Os900, a rice enzyme that converts the SL intermediate carlactone to 4DO. A Striga germination assay revealed that triflumizole-treated rice displayed a reduced level of germination stimulation for Striga. These results identify triflumizole as a novel lead compound for inhibition of SL biosynthesis. MDPI 2020-11-25 /pmc/articles/PMC7728069/ /pubmed/33255720 http://dx.doi.org/10.3390/molecules25235525 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
Kawada, Kojiro
Uchida, Yuya
Takahashi, Ikuo
Nomura, Takahito
Sasaki, Yasuyuki
Asami, Tadao
Yajima, Shunsuke
Ito, Shinsaku
Triflumizole as a Novel Lead Compound for Strigolactone Biosynthesis Inhibitor
title Triflumizole as a Novel Lead Compound for Strigolactone Biosynthesis Inhibitor
title_full Triflumizole as a Novel Lead Compound for Strigolactone Biosynthesis Inhibitor
title_fullStr Triflumizole as a Novel Lead Compound for Strigolactone Biosynthesis Inhibitor
title_full_unstemmed Triflumizole as a Novel Lead Compound for Strigolactone Biosynthesis Inhibitor
title_short Triflumizole as a Novel Lead Compound for Strigolactone Biosynthesis Inhibitor
title_sort triflumizole as a novel lead compound for strigolactone biosynthesis inhibitor
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7728069/
https://www.ncbi.nlm.nih.gov/pubmed/33255720
http://dx.doi.org/10.3390/molecules25235525
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