植物学报 ›› 2026, Vol. 61 ›› Issue (5): 871-882.DOI: 10.11983/CBB25144  cstr: 32102.14.CBB25144

• 技术方法 • 上一篇    下一篇

内蒙亚菊再生体系建立

郑萧岳, 孔丹睿, 邱悦, 赵惠恩*   

  1. 北京林业大学园林学院, 城乡生态环境北京实验室, 国家花卉工程技术研究中心, 花卉种质创新与分子育种北京市重点实验室, 北京 100083
  • 收稿日期:2025-08-07 接受日期:2026-01-09 发布日期:2026-01-12
  • 通讯作者: *赵惠恩, 教授, 博士生导师。主要从事大果无刺机采理想株型黑果枸杞基因编辑驯化和地被菊野化育种研究。在培育火星适宜菊花过程中获得了寒旱区保健牧草菊花多批授权新品种。E-mail: zhaohuien@bjfu.edu.cn
  • 基金资助:
    国家重点研发计划(No.2024YFF1308004)

Establishment of the Regeneration System of Ajania alabasica

Zheng Xiaoyue, Kong Danrui, Qiu Yue, Zhao Huien*   

  1. Beijing Key Laboratory of Flower Germplasm Innovation and Molecular Breeding, National Flower Engineering Technology Research Center, Beijing Laboratory of Urban and Rural Ecological Environment, College of Landscape Architecture, Beijing Forestry University, Beijing 100083, China
  • Received:2025-08-07 Accepted:2026-01-09 Published:2026-01-12
  • Contact: *E-mail: zhaohuien@bjfu.edu.cn

摘要: 内蒙亚菊(Ajania alabasica)为我国西北地区重要的野生菊花遗传资源, 具有良好的野化育种与抗性遗传研究价值, 但目前缺乏对其再生体系的研究。以内蒙亚菊野生植株的叶片和茎段为外植体, 进行再生体系研究。结果表明, 叶片较茎段更容易诱导出愈伤组织, 且不定芽分化率和繁殖系数较高。以叶片为外植体, 愈伤组织诱导和不定芽分化最适培养基为MS+1.0 mg∙L-1 6-BA+1.0 mg∙L-1 NAA, 接种15天愈伤组织诱导率可达100%, 接种30天不定芽分化率为92.22%, 繁殖系数达6.93。针对分化过程中的玻璃化现象, 研究发现0.3 mg∙L-1 6-BA+0.05 mg∙L-1 NAA为最优增殖培养基, 添加5 µmol∙L-1 AgNO3可缓解组培苗玻璃化。生根实验结果表明, 最佳生根培养基为1/2MS+0.2 mg∙L-1 NAA, 生根率为100%, 移栽成活率达88%。该研究成功建立了内蒙亚菊高效再生体系, 为其遗传转化和基因功能研究奠定了基础。

关键词: 内蒙亚菊, 再生体系, 玻璃化

Abstract: INTRODUCTION: Ajania alabasica is a wild species of the genus Ajania in the Asteraceae that is characterized by its remarkable drought resistance and ecological adaptability, making it a valuable genetic resource for breeding. Nevertheless, the absence of an effective in vitro regeneration system has impeded the advancement of rapid propagation and genetic transformation studies on this species.
RATIONALE: The utilization of appropriate explants constitutes a critical strategy for plant regeneration. The core of this methodology lies in optimizing the combinations of plant growth regulators (PGRs) and additives to balance differentiation and physiological disorders such as hyperhydricity. This study was conceived with the objective of systematically determining the effects of different explant types (leaves vs. stem segments) and PGRs, with a view to establishing a robust regeneration protocol for A. alabasica.
RESULTS: This study found that leaf explants exhibited significantly higher regeneration potential than stem segments. The results demonstrated that the optimal medium for callus induction and adventitious bud differentiation from leaves was MS basal medium supplemented with 1.0 mg∙L-1 6-BA and 1.0 mg∙L-1 NAA. Following the culture period, this resulted in a callus induction rate of 100% (at 15 days) and an adventitious bud differentiation rate of 92.22% with a multiplication coefficient of 6.93 (at 30 days). To address hyperhydricity, the optimal proliferation medium was identified as containing 0.3 mg∙L-1 6-BA and 0.05 mg∙L-1 NAA, with 5 µmol∙L-1 AgNO3 proving effective for alleviation. For the rooting phase, the optimal medium was identified as 1/2MS medium supplemented with 0.2 mg∙L-1 NAA, which resulted in a rooting rate of 100% and a transplant survival rate of 88%.
CONCLUSION: This study successfully established for the first time a highly efficient and stable regeneration system for A. alabasica using leaf explants. The developed system, characterized by its high differentiation and survival rates, provides crucial technical support for subsequent genetic transformation and gene function analysis.

Key words: Ajania alabasica, regeneration system, hyperhydricity