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独脚金内酯的化学与生物化学研究进展

Recent progress in the chemistry and biochemistry of strigolactones.

作者信息

Yoneyama Koichi

机构信息

Women's Future Development Center, Ehime University, 3 Bunkyo-cho, Matsuyama 790-8577, Japan.

出版信息

J Pestic Sci. 2020 May 20;45(2):45-53. doi: 10.1584/jpestics.D19-084.

DOI:10.1584/jpestics.D19-084
PMID:32508512
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7251197/
Abstract

Strigolactones (SLs) are plant secondary metabolites derived from carotenoids. SLs play important roles in the regulation of plant growth and development and coordinate interactions between plants and other organisms including root parasitic plants, and symbiotic and pathogenic microbes in the rhizosphere. In the 50 years since the discovery of the first SL, strigol, our knowledge about the chemistry and biochemistry of SLs has advanced explosively, especially over the last two decades. In this review, recent advances in the chemistry and biology of SLs are summarized and possible future outcomes are discussed.

摘要

独脚金内酯(SLs)是一类源自类胡萝卜素的植物次生代谢产物。独脚金内酯在植物生长发育调控中发挥着重要作用,并协调植物与其他生物之间的相互作用,这些生物包括根寄生植物以及根际中的共生微生物和致病微生物。自首个独脚金内酯——独脚金醇被发现后的50年间,我们对独脚金内酯的化学和生物化学知识的了解有了迅猛进展,尤其是在过去的二十年中。在这篇综述中,总结了独脚金内酯在化学和生物学方面的最新进展,并讨论了可能产生的未来成果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55ab/7251197/674f519a92ef/jps-45-2-D19-084-figure02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55ab/7251197/e3f2e6555e51/jps-45-2-D19-084-figure01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55ab/7251197/674f519a92ef/jps-45-2-D19-084-figure02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55ab/7251197/e3f2e6555e51/jps-45-2-D19-084-figure01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55ab/7251197/674f519a92ef/jps-45-2-D19-084-figure02.jpg

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Plant Direct. 2020 May 8;4(5):e00219. doi: 10.1002/pld3.219. eCollection 2020 May.
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CYP722C from Gossypium arboreum catalyzes the conversion of carlactonoic acid to 5-deoxystrigol.陆地棉 CYP722C 催化卡尔拉酮酸转化为 5-脱甲氧基野麦畏。
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Chemical identification of 18-hydroxycarlactonoic acid as an LjMAX1 product and in planta conversion of its methyl ester to canonical and non-canonical strigolactones in Lotus japonicus.
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Insights into stereoselective ring formation in canonical strigolactone: Identification of a dirigent domain-containing enzyme catalyzing orobanchol synthesis. canonical strigolactone 中环形成的立体选择性研究:鉴定一种含定向酶结构域的酶催化 Orobanchol 的合成。
Proc Natl Acad Sci U S A. 2024 Jun 25;121(26):e2313683121. doi: 10.1073/pnas.2313683121. Epub 2024 Jun 21.
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The structure-activity relationship of aryloxyacetylthioureas for the inhibition of radicle elongation.芳氧基乙酰基硫脲对胚根伸长抑制作用的构效关系
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