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植物研究 ›› 2026, Vol. 46 ›› Issue (2): 270-279.doi: 10.7525/j.issn.1673-5102.2026.02.007

• 研究论文column:Original Paper • 上一篇    下一篇

基于黄檗全基因组的苄基异喹啉生物碱生物合成相关O-甲基转移酶基因筛选及功能鉴定

曹畅1, 田亚2, 刘成伟2()   

  1. 1.东北林业大学化学化工与资源利用学院,哈尔滨 150040
    2.东北林业大学生命科学学院,哈尔滨 150040
  • 收稿日期:2025-10-24 出版日期:2026-03-20 发布日期:2026-04-02
  • 通讯作者: 刘成伟 E-mail:liuchw@nefu.edu.cn
  • 作者简介:曹畅(1987—),女,助理实验师,主要从事分析化学及天然产物化学研究。
  • 基金资助:
    国家自然科学基金面上项目(82274037)

Genome-wide Screening and Functional Verification of O-methyltransferase Genes Involved in Benzylisoquinoline Alkaloid Biosynthesis in Phellodendron amurense

Chang CAO1, Ya TIAN2, Chengwei LIU2()   

  1. 1.College of Chemistry,Chemical Engineer and Resource Utilization,Northeast Forestry University,Harbin 150040
    2.College of Life Sciences,Northeast Forestry University,Harbin 150040
  • Received:2025-10-24 Online:2026-03-20 Published:2026-04-02
  • Contact: Chengwei LIU E-mail:liuchw@nefu.edu.cn

摘要:

黄檗(Phellodendron amurense)是一种传统的药用树种,其富含的苄基异喹啉生物碱(BIA)具有显著的药理活性。O-甲基转移酶(OMT)是植物次生代谢中催化酚羟基甲基化的关键酶类,对苄基异喹啉生物碱结构多样化与稳定性具有重要作用。为系统解析黄檗OMT基因家族特征并挖掘参与BIA合成的关键基因,该研究基于黄檗全基因组数据,系统鉴定82个OMT基因家族成员。系统发育分析表明:所有成员均属于ClassⅠ类群,进一步划分为ClassⅠa和ClassⅠb 2个亚族。保守基序分析显示,2个亚族在保留核心SAM结合域的同时,其N端与C端基序组成存在显著差异。染色体定位分析表明:PaOMT基因呈不均匀分布且存在明显串联复制现象。结合黄檗多组织转录组数据筛选及体外酶活验证发现,PaOMT30能够催化(S)-金黄紫堇碱C-2位羟基的O-甲基化,生成(S)-四氢巴马汀红碱。该研究首次系统解析黄檗OMT基因家族特征,并明确PaOMT30在黄檗BIA合成途径中的C-2位甲基化活性,为阐明黄檗药用成分生物合成网络及BIA药物开发奠定了基础。

关键词: 黄檗, 苄基异喹啉生物碱, O-甲基转移酶, 甲基化, 功能表征

Abstract:

Phellodendron amurense is a traditional medicinal plant recognized for its abundant benzylisoquinoline alkaloids(BIAs), showing substantial pharmacological properties. O-methyltransferases(OMTs), pivotal enzymes in plant secondary metabolism, facilitate the methylation of phenolic hydroxyl groups and are crucial for the structural diversity and stability of BIAs. To comprehensively characterize the OMT gene family in P.amurense and identify key genes involved in BIA biosynthesis, this study performed a genome-wide analysis, identifying 82 OMT gene family members. Phylogenetic analysis indicated that all members belonged to the ClassⅠgroup, which can be further subdivided into two subgroups, ClassⅠa and ClassⅠb. Analysis of conserved motifs revealed that, while both subgroups maintained the core S-adenosylmethionine (SAM)-binding domain, they displayed notable differences in the composition of N- and C-terminal motifs. Chromosomal localization analysis illustrated the dispersed distribution of PaOMT genes. By integrating transcriptomic data from multiple tissues with in vitro enzymatic assays, PaOMT30 was identified to catalyze the O-methylation of the C-2 hydroxyl group of(S)-scoulerine, yielding(S)-tetrahydropalmatrubine. This study represented the first comprehensive analysis of the OMT gene family in P. amurense and successfully identified the C-2 methylation activity of PaOMT30 in BIA biosynthesis, establishing a foundation for elucidating the biosynthetic pathways of medicinal components in P.amurense and advancing BIA-based drug development.

Key words: Phellodendron amurense, benzylisoquinoline alkaloids, O-methyltransferase, methylation, functional characterization

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