植物学报

• 技术方法 • 上一篇    下一篇

楔叶菊再生体系建立

辜源馨1, 叶雨晴1, 徐俊1, 李毅1, 牛雅静2, 黄河1*   

  1. 1北京林业大学园林学院, 国家花卉工程技术研究中心, 城乡生态环境北京实验室, 花卉种质资源创新与分子育种北京市重点实验室, 北京100083; 2北京市植物园, 北京市花卉园艺工程技术研究中心, 北京100093
  • 收稿日期:2025-08-30 修回日期:2025-11-26 出版日期:2025-12-08 发布日期:2025-12-08
  • 通讯作者: 黄河
  • 基金资助:
    山东省重点研发计划(No.2024TZXD034)

Establishment of Regeneration System for Chrysanthemum naktongense

Yuanxin Gu1, Yuqing Ye1, Jun Xu1, Yi Li1, Yajing Niu2, He Huang1*   

  1. 1School of Landscape Architecture, Beijing Forestry University, National Engineering Research Center for Floriculture, Beijing Laboratory of Urban and Rural Ecological Environment, Beijing Key Laboratory of Ornamental Plants Germplasm Innovation& Molecular Breeding, Beijing 100083, China; 2Beijing Botanical Garden, Beijing Floriculture Engineering Technology Research Centre, Beijing 100093, China
  • Received:2025-08-30 Revised:2025-11-26 Online:2025-12-08 Published:2025-12-08
  • Contact: He Huang

摘要: 楔叶菊(Chrysanthemum naktongense)是菊科菊属野生种, 在扦插10天后能够快速形成根状茎, 是研究植物地下根状茎形成与发育分子机制的优异种质, 但目前缺少对其再生体系的研究。该研究以楔叶菊叶片为外植体, 探究不同植物生长调节剂组合及浓度对愈伤组织诱导和不定芽分化的影响, 并筛选出生根培养的最佳培养条件。结果表明, 楔叶菊叶片愈伤组织诱导和不定芽分化的最佳培养基为MS+0.5 mg∙L–1 6-BA+2.0 mg∙L–1 NAA, 接种45天后可形成1 cm以上再生芽, 再生率达100%; 最佳生根培养基为1/2MS+0.1 mg∙L–1 IBA, 再生芽生根率为100%。该研究建立了楔叶菊再生体系, 为根状茎形成和发育相关研究提供技术支撑。

关键词: 楔叶菊, 根状茎, 再生体系, 组织培养

Abstract: INTRODUCTION: Chrysanthemum naktongense is a wild species of the genus Chrysanthemum in the Asteraceae family, characterized by its remarkable capacity to rapidly form rhizomes within 10 days after cutting. Nevertheless, the absence of an effective in vitro regeneration system has impeded the advancement of genetic studies on this species.  RATIONALE: The utilisation of leaf discs as explants constitutes a well-established and effective strategy for plant regeneration. The core of this methodology lies in optimizing the combinations and concentrations of plant growth regulators (PGRs) in the culture medium, which critically demonstrated to influence the processes of callus induction, adventitious bud differentiation, and root formation. This study was conceived with the objective of systematically determining the effects of different PGRs, with a view to establishing a robust regeneration protocol for C. naktongense.  RESULTS: This study found that C. naktongense can form rhizomes after 10 days of cuttings and grow to 10 cm within 50 days. In this study, the results demonstrated that the optimal medium of leaf disc callus induction and adventitious bud differentiation was MS basal medium supplemented with 0.5 mg∙L–1 6-BA and 2.0 mg∙L–1 NAA. Following a 45-day treatment period, resulted in the induction of regenerated shoots that exceeded 1 cm in length, exhibiting a 100% regeneration rate. For the rooting phase, the optimal medium was identified as 1/2MS medium supplemented with 0.1 mg∙L–1 IBA, which also resulted in a rooting rate of 100%.  CONCLUSION: This study successfully established a highly efficient and stable regeneration system for C. naktongense, encompassing the stages from callus induction to plantlet rooting. The developed system, characterized by its 100% regeneration and rooting rates, provides crucial technical support for subsequent research.

Key words: Chrysanthemum naktongense, rhizome, regeneration system, tissue culture