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控制植物病原体的天然产物的生物有机化学

Bioorganic chemistry of natural products that control plant pathogens.

作者信息

Yajima Arata

机构信息

Department of Chemistry for Life Sciences and Agriculture, Faculty of Life Sciences, Tokyo University of Agriculture.

出版信息

J Pestic Sci. 2025 Aug 20;50(3):87-95. doi: 10.1584/jpestics.J25-03.

DOI:10.1584/jpestics.J25-03
PMID:40910014
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12405012/
Abstract

Developing new agrochemicals is essential for sustainable agriculture and global food security. Our group focused on natural products that control plant pathogens, conducting synthetic research across three key areas of interest: antimicrobial compounds, phytoalexins, and microbial signaling molecules. We established new methods for producing chiral allylic alcohols as useful synthetic intermediates for natural product synthesis the enantioselective synthesis of antimicrobial agents such as peniciaculins. In the phytoalexin research, the synthesis of biosynthetic intermediates enabled the elucidation of enzyme functions in terms of their biosynthesis and the confirmation of absolute configurations, deepening our understanding of plant defense systems. Furthermore, the total synthesis and biosynthetic studies of mating hormones revealed a unique chemical relay system regulating sexual reproduction. These findings emphasize the importance of synthetic chemistry in advancing natural product research and offer new strategies for crop protection. Our interdisciplinary approach paves the way for future innovations in combating agricultural pests and diseases.

摘要

开发新型农用化学品对可持续农业和全球粮食安全至关重要。我们的团队专注于控制植物病原体的天然产物,在三个关键研究领域开展合成研究:抗菌化合物、植保素和微生物信号分子。我们建立了生产手性烯丙醇的新方法,作为天然产物合成的有用合成中间体——如青霉环素等抗菌剂的对映选择性合成。在植保素研究中,生物合成中间体的合成使得能够从其生物合成方面阐明酶的功能并确认绝对构型,加深了我们对植物防御系统的理解。此外,交配激素的全合成和生物合成研究揭示了一种调节有性生殖的独特化学接力系统。这些发现强调了合成化学在推进天然产物研究中的重要性,并为作物保护提供了新策略。我们的跨学科方法为未来防治农业病虫害的创新铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba08/12405012/71b4ee46b1b2/jps-50-3-J25-03-figure05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba08/12405012/0d2aa31807b1/jps-50-3-J25-03-figure01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba08/12405012/a41c9d8a6b98/jps-50-3-J25-03-scheme01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba08/12405012/084d9f082f3d/jps-50-3-J25-03-figure02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba08/12405012/1e65697fee2e/jps-50-3-J25-03-scheme02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba08/12405012/4a095e222806/jps-50-3-J25-03-scheme03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba08/12405012/556da19ba151/jps-50-3-J25-03-figure03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba08/12405012/f625e61ec726/jps-50-3-J25-03-scheme04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba08/12405012/97e41d4dff08/jps-50-3-J25-03-figure04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba08/12405012/71b4ee46b1b2/jps-50-3-J25-03-figure05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba08/12405012/0d2aa31807b1/jps-50-3-J25-03-figure01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba08/12405012/a41c9d8a6b98/jps-50-3-J25-03-scheme01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba08/12405012/084d9f082f3d/jps-50-3-J25-03-figure02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba08/12405012/1e65697fee2e/jps-50-3-J25-03-scheme02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba08/12405012/4a095e222806/jps-50-3-J25-03-scheme03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba08/12405012/556da19ba151/jps-50-3-J25-03-figure03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba08/12405012/f625e61ec726/jps-50-3-J25-03-scheme04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba08/12405012/97e41d4dff08/jps-50-3-J25-03-figure04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba08/12405012/71b4ee46b1b2/jps-50-3-J25-03-figure05.jpg

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本文引用的文献

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Identification and evolution of a diterpenoid phytoalexin oryzalactone biosynthetic gene in the genus Oryza.在稻属中鉴定和演化二萜类植物抗毒素稻内酯生物合成基因。
Plant J. 2024 Apr;118(2):358-372. doi: 10.1111/tpj.16608. Epub 2024 Jan 9.
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Natural variation of diterpenoid phytoalexins in rice: Aromatic diterpenoid phytoalexins in specific cultivars.水稻二萜类植保素的自然变异:特定品种中的芳香二萜类植保素。
Phytochemistry. 2023 Jul;211:113708. doi: 10.1016/j.phytochem.2023.113708. Epub 2023 May 4.
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A dolabralexin-deficient mutant provides insight into specialized diterpenoid metabolism in maize.
一个缺失 dolabralexin 的突变体为玉米中特有的二萜类代谢提供了新的见解。
Plant Physiol. 2023 May 31;192(2):1338-1358. doi: 10.1093/plphys/kiad150.
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Synthesis and antifungal activity of the proposed structure of a volatile compound isolated from the edible mushroom .从食用蘑菇中分离出的一种挥发性化合物的拟议结构的合成及其抗真菌活性
J Pestic Sci. 2022 Feb 20;47(1):17-21. doi: 10.1584/jpestics.D21-061.
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Identification of biosynthetic intermediates for the mating hormone α2 of the plant pathogen Phytophthora.鉴定植物病原菌卵菌交配激素α2的生物合成中间产物。
Biosci Biotechnol Biochem. 2021 Jul 23;85(8):1802-1808. doi: 10.1093/bbb/zbab098.
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Disproof of the Proposed Structures of Bradyoxetin, a Putative Signaling Molecule, and HMCP, a Putative Quorum-Sensing Molecule.否定拟信号分子布雷地辛和拟群体感应分子 HMCP 的提出结构。
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