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桉树林分密度对林下套种五指毛桃次生代谢与抗氧化活性的影响

Effects of Eucalyptus Stand Density on Secondary Metabolism and Antioxidant Activity in Intercropped Ficus hirta

  • 摘要: 以尾巨桉人工林为对象,设置TT(1650株/hm2)、FR(1125株/hm2)2种林分密度处理及全光照对照(CK),测定林下五指毛桃根系中总酚、总黄酮及佛手柑内酯、补骨脂素等生物活性成分含量,并系统评估其体外抗氧化活性;结合非靶向代谢组学技术,解析其次生代谢物组成,筛选与抗氧化能力显著相关的关键代谢物质。结果表明:TT处理显著促进了五指毛桃生物活性成分的积累,总酚和总黄酮含量分别较CK提高108.3%和30.2%,质控成分佛手苷内酯与补骨脂素含量较CK分别显著增加25.40%和17.6%;TT处理下DPPH、ABTS自由基清除能力及总抗氧化能力均表现最优。基于代谢组学分析,共鉴定出1852种代谢物,其中TT处理引起代谢谱显著扰动,差异代谢物数量明显多于FR处理。KEGG通路富集分析显示,TT处理显著激活了苯丙烷生物合成和黄酮类化合物生物合成途径,从中鉴定出45种酚酸类和20种黄酮类差异代谢物,其中28种酚酸显著上调;筛选出4−甲氧基肉桂醛、1,3−O−双咖啡酰奎宁酸、没食子酸等11种酚类成分以及桑黄酮C、4−羟基查尔酮等8种黄酮类成分,这些成分与五指毛桃抗氧化能力显著相关。

     

    Abstract:
    Taking Eucalyptus urophylla × E. grandis plantations as the research object, two stand density treatments including TT (1650 trees/hm2) and FR (1125 trees/hm2), as well as a full sunlight control group (CK), were established. The contents of bioactive components such as total phenols, total flavonoids, bergapten and psoralen in the roots of Ficus hirta growing under the forest were determined, and their in vitro antioxidant activities were systematically evaluated. Untargeted metabolomics was further applied to analyze the composition of secondary metabolites and screen key metabolites significantly associated with antioxidant capacity. The results showed that the TT treatment significantly promoted the accumulation of bioactive components in F. hirta. Compared with CK, the contents of total phenols and total flavonoids increased by 108.3% and 30.2%, respectively. The contents of quality control markers bergapten and psoralen were markedly elevated by 25.40% and 17.6% relative to CK. Meanwhile, the TT group exhibited the highest DPPH radical scavenging activity, ABTS radical scavenging activity and total antioxidant capacity.
    A total of 1852 metabolites were identified via metabolomic analysis. The metabolic profile was profoundly altered under TT treatment, with a greater number of differentially expressed metabolites (DEMs) than that under FR treatment. KEGG pathway enrichment analysis revealed that the phenylpropanoid biosynthesis and flavonoid biosynthesis pathways were significantly activated in the TT group. A total of 45 phenolic acids and 20 flavonoids were identified as DEMs, among which 28 phenolic acids were significantly upregulated. Furthermore, 11 phenolic compounds (e.g., 4-methoxycinnamaldehyde, 1,3-O-dicaffeoylquinic acid and gallic acid) and 6 flavonoids (e.g., morusflavone C and 4-hydroxychalcone) were screened out, which were closely correlated with the antioxidant capacity of F. hirta.

     

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