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刺五加苷B生物合成途径的代谢组学和转录组学分析 于……中 (原文句子不完整,“in”后面缺少具体内容)

Metabolome and transcriptome analysis of eleutheroside B biosynthesis pathway in .

作者信息

Guo Hong-Yu, Zhang Jie, Lin Li-Mei, Song Xin, Zhang Duo-Duo, Cui Ming-Hui, Long Chang-Wen, Long Yue-Hong, Xing Zhao-Bin

机构信息

College of Life Sciences, North China University of Science and Technology, Tangshan, China.

Hebeidingzhou High School, Dingzhou, China.

出版信息

Heliyon. 2022 Jun 6;8(6):e09665. doi: 10.1016/j.heliyon.2022.e09665. eCollection 2022 Jun.

Abstract

Eleutheroside B (syringin) is a medicinal active ingredient extracted from (Ruper. et Maxim.) Maxim with high clinical application value. However, its synthesis pathway remains unknown. Here, we analyzed the eleutheroside B biosynthesis pathway in . Consequently, metabolomic and transcriptomic analyses identified 461 differentially expressed genes (DEGs) and 425 metabolites. Further, we identified 7 DEGs and 67 metabolites involved in the eleutheroside B biosynthetic pathway in the eleutheroside B high and low plants. The correlation between the gene and metabolites was explored using the pearson correlation coefficient (PCC) analysis. Caffeoyl-CoA O-methyltransferase, caffeic acid-O-methyltransferase, β-amyrin synthase (β-AS) genes, NAC5, and HB5 transcription factors were identified as candidate genes and transcription factors related to the eleutheroside B synthesis. Eleutheroside B content was the highest at the young stage of the leaves both in the high and low eleutheroside B plants. Quantitative real-time polymerase chain reaction revealed that phenylalanine ammonia-lyase1, cinnamate 4-hydroxylase, , and leucoanthocyanidin reductase gene had higher expression levels at the young stage of the leaves in the low eleutheroside B plants but lower expression levels in the high eleutheroside B plants. In the present study, we complemented the eleutheroside B biosynthetic pathway by analyzing the expression levels of relevant genes and metabolite accumulation patterns.

摘要

刺五加苷B(紫丁香苷)是从刺五加(Ruper. et Maxim.)Maxim中提取的一种具有高临床应用价值的药用活性成分。然而,其合成途径仍然未知。在此,我们分析了刺五加中刺五加苷B的生物合成途径。因此,代谢组学和转录组学分析鉴定出461个差异表达基因(DEGs)和425种代谢物。此外,我们在刺五加苷B含量高和低的植株中鉴定出7个参与刺五加苷B生物合成途径的DEGs和67种代谢物。使用皮尔逊相关系数(PCC)分析探索了基因与代谢物之间的相关性。咖啡酰辅酶A O-甲基转移酶、咖啡酸-O-甲基转移酶、β-香树脂醇合酶(β-AS)基因、NAC5和HB5转录因子被鉴定为与刺五加苷B合成相关的候选基因和转录因子。在刺五加苷B含量高和低的植株中,叶片幼嫩阶段的刺五加苷B含量最高。定量实时聚合酶链反应显示,苯丙氨酸解氨酶1、肉桂酸4-羟化酶、 以及无色花青素还原酶基因在刺五加苷B含量低的植株叶片幼嫩阶段表达水平较高,但在刺五加苷B含量高的植株中表达水平较低。在本研究中,我们通过分析相关基因的表达水平和代谢物积累模式,完善了刺五加苷B的生物合成途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/485a/9190005/614bc90fedd5/gr1.jpg

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