生物技术通报 ›› 2026, Vol. 42 ›› Issue (7): 173-181.doi: 10.13560/j.cnki.biotech.bull.1985.2025-0874

• 研究报告 • 上一篇    

基于非靶向代谢组解析红花石蒜叶片对高温胁迫的响应

游欣1(), 王淅1, 张新妤1, 魏绪英2, 程华1(), 蔡军火1()   

  1. 1.江西农业大学园林与艺术学院,南昌 330045
    2.江西财经大学艺术学院,南昌 330032
  • 收稿日期:2025-08-11 出版日期:2026-07-26 发布日期:2026-07-20
  • 通讯作者: 蔡军火Cjhuo7692@163.com
    程华chenghua0802@sina.com
    蔡军火,男,教授,研究方向 :植物栽培生理与花期调控;E-mail: Cjhuo7692@163.com
    程华,女,博士,青年教授,研究方向 :观赏植物遗传育种与分子生物学;E-mail: Chenghua0802@sina.com
  • 作者简介:游欣,女,博士研究生,研究方向 :植物栽培生理与花期调控;E-mail: youxin0428@163.com
  • 基金资助:
    国家自然科学基金项目(32360420);农业农村部花卉生物学与种质创制重点实验室开放基金(KFF202401)

Analysis of Response of Lycoris radiata Leaves to Heat Stress Revealed by Untargeted Metabolomics

YOU Xin1(), WANG Xi1, ZHANG Xin-yu1, WEI Xu-ying2, CHENG Hua1(), CAI Jun-huo1()   

  1. 1.College of Landscape Architecture and Art, Jiangxi Agricultural University, Nanchang 330045
    2.College of Art, Jiangxi University of Finance and Economics, Nanchang 330032
  • Received:2025-08-11 Published:2026-07-26 Online:2026-07-20

摘要:

目的 揭示高温胁迫下石蒜属植物叶片的代谢响应特征及相关通路,为培育耐极端高温生境的石蒜属新种质提供理论依据。 方法 以红花石蒜为试验材料,于人工气候培养箱中进行42 ℃高温处理,并分别于处理0 h(对照)、6 h和12 h采集叶片样品,通过LC-MS技术进行非靶向代谢组学分析。 结果 在3个比较组(HS_6 h vs HS_0 h、HS_12 h vs HS_0 h和HS_12 h vs HS_6 h)中分别筛选出338、426、262种差异代谢物。在高温胁迫初期(42 ℃,6 h),差异代谢物活性整体上被显著抑制,而在高温胁迫后期(42 ℃,12 h)则转向以上调为主导的代谢重编程。进一步分析表明,脂类和氨基酸及其衍生物是高温胁迫的主要差异代谢物类别,其中脂类在胁迫初期以下调为主导,而氨基酸及其衍生物则在胁迫后期呈现显著上调积累。KEGG代谢通路富集分析显示,高温胁迫诱导的差异代谢物主要参与由“磷脂酰胆碱水解驱动”的脂质代谢途径(含亚油酸代谢、花生四烯酸代谢、α-亚麻酸代谢和甘油磷脂代谢4条支路)和以多种氨基酸(L-脯氨酸、L-苯丙氨酸等)显著积累为特征的氨基酸代谢途径(主要包括氨酰-tRNA生物合成、D-氨基酸代谢和苯丙氨酸代谢3条支路)及次生代谢物的生物合成。 结论 红花石蒜通过“脂质介导的持续膜稳态调控”结合“后期氨基酸驱动的防御网络强化”的协同策略,共同构建其高温适应性网络。

关键词: 红花石蒜, 高温胁迫, 代谢组学, 脂类代谢, 氨基酸代谢

Abstract:

Objective To decipher the metabolic response characteristics and associated pathways in Lycoris leaves under heat stress, and to provide a theoretical basis for cultivating new Lycoris germplasm that can tolerate extreme high-temperature habitats. Method Using Lycoris radiata as plant material, heat stress treatment was conducted at 42 ℃ in a controlled environment chamber. Leaf samples were collected at 0 h (control), 6 h, and 12 h after treatment initiation, followed by untargeted metabolomics profiling via LC-MS technology. Result Across three comparison groups (HS_6 h vs HS_0 h, HS_12 h vs HS_0 h, and HS_12 h vs HS_6 h), 338, 426, and 262 differential metabolites were identified, respectively. During early heat stress (42 ℃, 6 h), metabolic activity was significantly suppressed overall. Conversely, prolonged exposure (42 ℃, 12 h) triggered a metabolic reprogramming shift dominated by up-regulation. Further analysis revealed that lipids, amino acids and derivatives constituted the major classes of differential metabolites under heat stress. Notably, lipids were mainly down-regulated during the initial phase of heat stress, whereas amino acids and derivatives showed significant up-regulation and accumulation in the later stress stage. KEGG pathway enrichment analysis revealed that heat stress-induced differential metabolites were primarily enriched in: Lipid metabolic pathways driven by phosphatidylcholine hydrolysis (encompassing four sub-pathways: Linoleic acid metabolism, arachidonic acid metabolism, alpha-linolenic acid metabolism, and glycerophospholipid metabolism), amino acid metabolic pathways characterized by significant accumulation of multiple amino acids (e.g., L-proline, L-phenylalanine) (involving three core sub-pathways: Aminoacyl-tRNA biosynthesis, D-amino acid metabolism and phenylalanine metabolism) and biosynthesis of secondary metabolites. Conclusion L. radiata employs a synergistic strategy combining “lipid-mediated sustained regulation of membrane homeostasis” with “reinforcement of amino acid-driven defense networks in later stages” to collectively establish its thermal adaptation network.

Key words: Lycoris radiata, heat stress, metabolomics, lipid metabolism, amino acid metabolism