Triflumizole as a Novel Lead Compound for Strigolactone Biosynthesis Inhibitor

斯特里加 生物合成 司他内酯 发芽 生物 奥罗班切 内生 斯特里加·赫蒙蒂卡 生物化学 植物 突变体 拟南芥 基因
作者
Kojiro Kawada,Yuya Uchida,Ikuo Takahashi,T. Nomura,Yasuyuki Sasaki,Tadao Asami,Shunsuke Yajima,Shinsaku Ito
出处
期刊:Molecules [MDPI AG]
卷期号:25 (23): 5525-5525 被引量:11
标识
DOI:10.3390/molecules25235525
摘要

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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