Sustainable Natural Resources for Aphid Management: β-Ionone and Its Derivatives as Promising Ecofriendly Botanical-Based Products

IF 5.7 1区 农林科学 Q1 AGRICULTURE, MULTIDISCIPLINARY Journal of Agricultural and Food Chemistry Pub Date : 2024-09-24 DOI:10.1021/acs.jafc.4c04053
Shi-Xiang Pan, Cheng Qu, Yan Liu, Zhuo Shi, Xing-Xing Lu, Zhao-Kai Yang, Xiao-Bo Huang, Wan Li, Xue-Sheng Li, Zheng-Xin Zhou, Chen Chen, Chen Luo, Yao-Guo Qin, Xin-Ling Yang
{"title":"Sustainable Natural Resources for Aphid Management: β-Ionone and Its Derivatives as Promising Ecofriendly Botanical-Based Products","authors":"Shi-Xiang Pan, Cheng Qu, Yan Liu, Zhuo Shi, Xing-Xing Lu, Zhao-Kai Yang, Xiao-Bo Huang, Wan Li, Xue-Sheng Li, Zheng-Xin Zhou, Chen Chen, Chen Luo, Yao-Guo Qin, Xin-Ling Yang","doi":"10.1021/acs.jafc.4c04053","DOIUrl":null,"url":null,"abstract":"β-Ionone, sustainably derived from <i>Petunia hybrida</i> as a natural bioresource, was identified as a lead compound for integrated aphid management. A series of β-ionone derivatives containing ester groups were designed and synthesized for the purpose of discovering renewable botanical-based products. The odorant-binding protein (OBP) binding test indicated that β-ionone and its derivatives displayed binding affinities with <i>Acyrthosiphon pisum</i> OBP9 (ApisOBP9) and <i>Harmonia axyridis</i> OBP15 (HaxyOBP15). Bioactivity assays revealed that most β-ionone derivatives exhibited a higher repellent activity than that of β-ionone. β-Ionone and derivatives <b>4g</b> and <b>4l</b> displayed attractiveness to <i>H. axyridis</i>. Specifically, <b>4g</b> was a highly promising derivative, possessing good repellent activity against <i>A. pisum</i> and attractiveness to <i>H. axyridis</i>. Molecular dynamics simulations revealed that integrating the hydrophobic ester group into the β-ionone framework strengthened the van der Waals interactions of <b>4g</b> with ApisOBP9/HaxyOBP15, improving the binding affinity with OBPs and producing higher push–pull activity than β-ionone; <b>4g</b> also had low toxicity toward nontarget organisms. Thus, <b>4g</b> is a potential ecofriendly, botanical-based option for aphid management.","PeriodicalId":41,"journal":{"name":"Journal of Agricultural and Food Chemistry","volume":null,"pages":null},"PeriodicalIF":5.7000,"publicationDate":"2024-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Agricultural and Food Chemistry","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1021/acs.jafc.4c04053","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"AGRICULTURE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

β-Ionone, sustainably derived from Petunia hybrida as a natural bioresource, was identified as a lead compound for integrated aphid management. A series of β-ionone derivatives containing ester groups were designed and synthesized for the purpose of discovering renewable botanical-based products. The odorant-binding protein (OBP) binding test indicated that β-ionone and its derivatives displayed binding affinities with Acyrthosiphon pisum OBP9 (ApisOBP9) and Harmonia axyridis OBP15 (HaxyOBP15). Bioactivity assays revealed that most β-ionone derivatives exhibited a higher repellent activity than that of β-ionone. β-Ionone and derivatives 4g and 4l displayed attractiveness to H. axyridis. Specifically, 4g was a highly promising derivative, possessing good repellent activity against A. pisum and attractiveness to H. axyridis. Molecular dynamics simulations revealed that integrating the hydrophobic ester group into the β-ionone framework strengthened the van der Waals interactions of 4g with ApisOBP9/HaxyOBP15, improving the binding affinity with OBPs and producing higher push–pull activity than β-ionone; 4g also had low toxicity toward nontarget organisms. Thus, 4g is a potential ecofriendly, botanical-based option for aphid management.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
用于治理蚜虫的可持续自然资源:β-壬酮及其衍生物是前景看好的生态友好型植物产品
从矮牵牛杂交种中可持续提取的β-葱酮是一种天然生物资源,被确定为蚜虫综合治理的先导化合物。为了发现基于植物的可再生产品,我们设计并合成了一系列含有酯基的 β-ionone 衍生物。气味结合蛋白(OBP)结合试验表明,β-ionone 及其衍生物与 Acyrthosiphon pisum OBP9(ApisOBP9)和 Harmonia axyridis OBP15(HaxyOBP15)具有结合亲和力。生物活性测定显示,大多数 β-ionone 衍生物的驱虫活性高于 β-ionone 衍生物。β-ionone 及其衍生物 4g 和 4l 对 H. axyridis 具有吸引力。具体来说,4g 是一种极具潜力的衍生物,对 A. pisum 具有良好的驱避活性,对 H. axyridis 具有吸引力。分子动力学模拟显示,将疏水酯基团整合到 β-ionone 框架中可加强 4g 与 ApisOBP9/HaxyOBP15 的范德华相互作用,提高与 OBPs 的结合亲和力,并产生比 β-ionone 更高的推拉活性;4g 对非目标生物的毒性也很低。因此,4g 是一种潜在的生态友好型植物性蚜虫防治方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Journal of Agricultural and Food Chemistry
Journal of Agricultural and Food Chemistry 农林科学-农业综合
CiteScore
9.90
自引率
8.20%
发文量
1375
审稿时长
2.3 months
期刊介绍: The Journal of Agricultural and Food Chemistry publishes high-quality, cutting edge original research representing complete studies and research advances dealing with the chemistry and biochemistry of agriculture and food. The Journal also encourages papers with chemistry and/or biochemistry as a major component combined with biological/sensory/nutritional/toxicological evaluation related to agriculture and/or food.
期刊最新文献
Characterization and Molecular Engineering of a N-Methyltransferase from Edible Nelumbo nucifera Leaves Involved in Nuciferine Biosynthesis. Characterization of Potent Odorants Causing an Oily Odor in Rice-Made Baijiu by Comparative Aroma Extract Dilution Analysis, Quantitative Measurements, and Aroma Addition and Omission Studies. Enzymatic Production of Trehalose and Trehalulose by Immobilized Thermostable Trehalose Synthase. From Proline to Chlorantraniliprole Mimics: Computer-Aided Design, Simple Preparation, and Excellent Insecticidal Profiles. Gallic Acid Alleviates Glucolipotoxicity-Induced Nephropathy by miR-709-NFE2L2 Pathway in db/db Mice on a High-Fat Diet.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1