代谢物分析表明黄酮类化合物和游离脂肪酸在香梨水分亏缺胁迫反应中的作用

IF 1.7 4区 生物学 Q3 ECOLOGY
Flora Pub Date : 2025-04-21 DOI:10.1016/j.flora.2025.152729
Jing Cao , Zhensong Li , Thomas A. Monaco , Yuping Rong
{"title":"代谢物分析表明黄酮类化合物和游离脂肪酸在香梨水分亏缺胁迫反应中的作用","authors":"Jing Cao ,&nbsp;Zhensong Li ,&nbsp;Thomas A. Monaco ,&nbsp;Yuping Rong","doi":"10.1016/j.flora.2025.152729","DOIUrl":null,"url":null,"abstract":"<div><div>Each spiny bur of <em>Cenchrus spinifex</em> Cav. (field sandbur) typically contains two seeds: a relatively large seed resembling a mango (M-type seed), and a relatively small seed resembling a pear (P-type seed). Metabolic variations arising from seed heteromorphism are regarded as crucial adaptive strategies enabling plants to thrive in unpredictable conditions. Nevertheless, metabolic studies on <em>C. spinifex</em> remain scarce. In this study, we utilized an untargeted metabolomics analysis by UHPLC-MS/MS to delineate the metabolic profiles associated with water deficit stress response in M- and P-type seedlings of <em>C. spinifex.</em> Seedlings were exposed to three watering regimes equating to 65–70 %, 45–50 %, and 25–30 % soil water-holding capacity. M-type seedlings prioritized root biomass allocation under stress, while P-type seedlings favored spikelet production, reflecting divergent survival–reproduction trade-offs. Metabolomic profiling revealed 43 differentially accumulated metabolites, with flavonoids as key discriminators between seedling types. In summary, <em>C. spinifex</em> exhibits pronounced metabolic divergence under water deficit stress, with flavonoids and free fatty acids serving as central adaptive metabolites. Crucially, flavonoids emerged as the key differential factor between M- and P-type seedlings. These findings demonstrate that seed heteromorphism in <em>C. spinifex</em> drives differential metabolic and allocation strategies, enhancing drought resilience and invasion success in arid environments.</div></div>","PeriodicalId":55156,"journal":{"name":"Flora","volume":"327 ","pages":"Article 152729"},"PeriodicalIF":1.7000,"publicationDate":"2025-04-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Metabolite analysis indicates role of flavones and free fatty acids in water deficit stress response of Cenchrus spinifex\",\"authors\":\"Jing Cao ,&nbsp;Zhensong Li ,&nbsp;Thomas A. Monaco ,&nbsp;Yuping Rong\",\"doi\":\"10.1016/j.flora.2025.152729\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Each spiny bur of <em>Cenchrus spinifex</em> Cav. (field sandbur) typically contains two seeds: a relatively large seed resembling a mango (M-type seed), and a relatively small seed resembling a pear (P-type seed). Metabolic variations arising from seed heteromorphism are regarded as crucial adaptive strategies enabling plants to thrive in unpredictable conditions. Nevertheless, metabolic studies on <em>C. spinifex</em> remain scarce. In this study, we utilized an untargeted metabolomics analysis by UHPLC-MS/MS to delineate the metabolic profiles associated with water deficit stress response in M- and P-type seedlings of <em>C. spinifex.</em> Seedlings were exposed to three watering regimes equating to 65–70 %, 45–50 %, and 25–30 % soil water-holding capacity. M-type seedlings prioritized root biomass allocation under stress, while P-type seedlings favored spikelet production, reflecting divergent survival–reproduction trade-offs. Metabolomic profiling revealed 43 differentially accumulated metabolites, with flavonoids as key discriminators between seedling types. In summary, <em>C. spinifex</em> exhibits pronounced metabolic divergence under water deficit stress, with flavonoids and free fatty acids serving as central adaptive metabolites. Crucially, flavonoids emerged as the key differential factor between M- and P-type seedlings. These findings demonstrate that seed heteromorphism in <em>C. spinifex</em> drives differential metabolic and allocation strategies, enhancing drought resilience and invasion success in arid environments.</div></div>\",\"PeriodicalId\":55156,\"journal\":{\"name\":\"Flora\",\"volume\":\"327 \",\"pages\":\"Article 152729\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2025-04-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Flora\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0367253025000593\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"ECOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Flora","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0367253025000593","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ECOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

刺竹属的每根刺。(田间沙砾)通常包含两个种子:一个相对较大的种子,类似芒果(m型种子),一个相对较小的种子,类似梨(p型种子)。由种子异型性引起的代谢变异被认为是使植物在不可预测的条件下茁壮成长的关键适应策略。然而,关于棘棘草的代谢研究仍然很少。本研究利用超高效液相色谱-质谱联用技术(UHPLC-MS/MS)对棘草M型和p型幼苗水分亏缺胁迫响应的代谢谱进行了分析。幼苗暴露在三种灌溉制度下,分别为65 - 70%、45 - 50%和25 - 30%的土壤保水能力。m型幼苗在逆境下优先分配根系生物量,而p型幼苗更倾向于产生小穗,这反映了不同的生存与繁殖权衡。代谢组学分析显示43种代谢物的积累差异,黄酮类化合物是幼苗类型之间的关键鉴别因子。综上所述,在水分亏缺胁迫下,刺荆草表现出明显的代谢分化,黄酮类化合物和游离脂肪酸是主要的适应性代谢产物。关键是,黄酮类化合物是M型和p型幼苗之间的关键差异因子。这些结果表明,刺花种子的异型性驱动了不同的代谢和分配策略,增强了干旱环境下的抗旱性和入侵成功率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Metabolite analysis indicates role of flavones and free fatty acids in water deficit stress response of Cenchrus spinifex
Each spiny bur of Cenchrus spinifex Cav. (field sandbur) typically contains two seeds: a relatively large seed resembling a mango (M-type seed), and a relatively small seed resembling a pear (P-type seed). Metabolic variations arising from seed heteromorphism are regarded as crucial adaptive strategies enabling plants to thrive in unpredictable conditions. Nevertheless, metabolic studies on C. spinifex remain scarce. In this study, we utilized an untargeted metabolomics analysis by UHPLC-MS/MS to delineate the metabolic profiles associated with water deficit stress response in M- and P-type seedlings of C. spinifex. Seedlings were exposed to three watering regimes equating to 65–70 %, 45–50 %, and 25–30 % soil water-holding capacity. M-type seedlings prioritized root biomass allocation under stress, while P-type seedlings favored spikelet production, reflecting divergent survival–reproduction trade-offs. Metabolomic profiling revealed 43 differentially accumulated metabolites, with flavonoids as key discriminators between seedling types. In summary, C. spinifex exhibits pronounced metabolic divergence under water deficit stress, with flavonoids and free fatty acids serving as central adaptive metabolites. Crucially, flavonoids emerged as the key differential factor between M- and P-type seedlings. These findings demonstrate that seed heteromorphism in C. spinifex drives differential metabolic and allocation strategies, enhancing drought resilience and invasion success in arid environments.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Flora
Flora 生物-植物科学
CiteScore
3.30
自引率
10.50%
发文量
130
审稿时长
54 days
期刊介绍: FLORA publishes original contributions and review articles on plant structure (morphology and anatomy), plant distribution (incl. phylogeography) and plant functional ecology (ecophysiology, population ecology and population genetics, organismic interactions, community ecology, ecosystem ecology). Manuscripts (both original and review articles) on a single topic can be compiled in Special Issues, for which suggestions are welcome. FLORA, the scientific botanical journal with the longest uninterrupted publication sequence (since 1818), considers manuscripts in the above areas which appeal a broad scientific and international readership. Manuscripts focused on floristics and vegetation science will only be considered if they exceed the pure descriptive approach and have relevance for interpreting plant morphology, distribution or ecology. Manuscripts whose content is restricted to purely systematic and nomenclature matters, to geobotanical aspects of only local interest, to pure applications in agri-, horti- or silviculture and pharmacology, and experimental studies dealing exclusively with investigations at the cellular and subcellular level will not be accepted. Manuscripts dealing with comparative and evolutionary aspects of morphology, anatomy and development are welcome.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信