Bioconversion of 5-deoxystrigol stereoisomers to monohydroxylated strigolactones by plants
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- Ueno Kotomi
- Graduate School of Agricultural Science, Kobe University
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- Nakashima Hitomi
- Graduate School of Agricultural Science, Kobe University
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- Mizutani Masaharu
- Graduate School of Agricultural Science, Kobe University
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- Takikawa Hirosato
- Graduate School of Agricultural Science, Kobe University
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- Sugimoto Yukihiro
- Graduate School of Agricultural Science, Kobe University
Bibliographic Information
- Other Title
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- 植物による5-デオキシストリゴールの立体選択的な水酸化
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Abstract
<p>The bioconversion of 5-deoxystrigol (5DS) and 4-deoxyorobanchol (4DO), the simplest canonical strigolactones (SLs), into monohydroxylated SLs such as strigol, sorgomol and orobanchol was confirmed by administering of stable isotope-labeled substrates to hydroponically grown plants. Liquid chromatography-mass spectrometry analyses established that 5DS was stereoselectively converted into strigol and sorgomol by cotton (Gossypium hirsutum) and Chinese milk vetch (Astragalus sinicus), respectively. 4DO was converted into orobanchol by rice (Oryza sativa). However, the red bell pepper (Capsicum annuum), red clover (Trifolium pratense), and pea (Pisum sativum) negligibly converted 4DO into orobanchol. The red bell pepper converted ent-4DO into 2′,8-bisepi-sorgomol. These results suggest that some plants generate orobanchol without passing through 4DO.</p>
Journal
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- Journal of Pesticide Science
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Journal of Pesticide Science 43 (3), 198-206, 2018-08-20
Pesticide Science Society of Japan
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Details 詳細情報について
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- CRID
- 1390282763033900160
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- NII Article ID
- 130007437208
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- NII Book ID
- AA11818622
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- ISSN
- 13490923
- 03851559
- 1348589X
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- NDL BIB ID
- 029353517
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- Text Lang
- en
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- Data Source
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- JaLC
- NDL
- Crossref
- CiNii Articles
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- Abstract License Flag
- Disallowed