中国农业科技导报 ›› 2019, Vol. 21 ›› Issue (10): 157-162.DOI: 10.13304/j.nykjdb.2018.0386

• 方法与技术创新 • 上一篇    下一篇

杜仲愈伤组织诱导及增殖培养技术研究

张海波1,胡燕花2,张国禹1,陈世林3,吴笛1,张定军1,黄桂云1*,张本厚2*   

  1. 1.长江珍稀植物研究所三峡集团流域枢纽运行管理局, 湖北 宜昌 443001; 2.南京工业大学大丰海洋产业研究院, 江苏 盐城 224145; 3.湖北省宜昌市夷陵区植物保护站, 湖北 宜昌 443000
  • 收稿日期:2018-06-26 出版日期:2019-10-15 发布日期:2018-08-02
  • 通讯作者: *通信作者:黄桂云,高级工程师,研究方向为长江流域珍稀濒危植物研究。E-mail: huang_guiyun@ctg.com.cn; 张本厚,助理研究员,研究方向为植物组织培养。E-mail: zhangbenhou@163.com
  • 作者简介:张海波,工程师,硕士,研究方向为三峡珍稀、濒危植物繁育与保护。E-mail: 272612886@qq.com。
  • 基金资助:
    江苏省盐土(滩涂)重点实验室开放课题项目(JKLB2018005)资助。

Study on Callus Induction and Proliferation Culture of Eucommia ulmoides

ZHANG Haibo1, HU Yanhua2, ZHANG Guoyu1, CHEN Shilin3, WU Di1, ZHANG Dingjun1, HUANG Guiyun1*, ZHANG Benhou2*   

  1. 1.Rare Plant Research Institute of the Yangtze River, Hubei Yichang 443001; 2.Dafeng Marine Industrial Institute, Nanjing Technology University, Jiangsu Yancheng 224100; 3.Plant Protection Station of Yiling District of Hubei Province, Hubei Yichang 443000, China
  • Received:2018-06-26 Online:2019-10-15 Published:2018-08-02

摘要: 杜仲是我国名贵的中药材和最有开发前景的胶源植物。通过筛选外植体、优化培养基,建立杜仲愈伤组织诱导和增殖的培养体系,利用统计学方法进行分析。结果显示:以子叶、幼叶、下胚轴为外植体均能够诱导出愈伤组织,但较佳的外植体为下胚轴,诱导率达到79.33%;以下胚轴为外植体的愈伤组织诱导基本培养基是B5,较优的激素配比为NAA 1.0 mg/L+2,4-D 2.0 mg/L;愈伤组织增殖培养的较优激素配比为6-BA 0.5 mg/L+NAA 0.5 mg/L+2,4-D 1.0 mg/L。建立了杜仲愈伤组织的培养方法,为通过杜仲细胞培养获得代谢产物提供了技术支持。

关键词: 杜仲, 愈伤组织, 增殖培养

Abstract: Eucommia ulmoides is one of the most valuable Chinese medicinal materials and the most promising gum source plants. In this paper, the culture system of callus induction and proliferation of Eucommia ulmoides was established by screening explants and optimizing the culture medium. The results showed that cotyledons, leaves and hypocotyls could induce callus, but the better explants were hypocotyls. The better basal medium for callus induction was B5, and the optimal phytohormones were NAA 1.0 mg/L and 2, 4-D 2.0 mg/L. The optimal phytohormone for callus proliferation culture were 6-BA 0.5 mg/L, NAA 0.5 mg/L and 2,4-D 1.0 mg/L. This paper established a method for callus culture of Eucommia ulmoides Oliv., which provided technical support for obtaining metabolites through cell culture.

Key words: Eucommia ulmoides, callus, proliferative culture