Subtropical Plant Science ›› 2019, Vol. 48 ›› Issue (01): 84-87.DOI: 10.3969/j.issn.1009-7791.2019.01.016

• Plant tissue culture and plant protection • Previous Articles     Next Articles

Screening Optimal Medium for Inducing Callus and Buds of Polygonatum cyrtonema

YE Yu-xin, REN Meng-ting, YI Wei-hao, QI Qing, PENG Dai-yin, XING Shi-hai   

  1. (1.College of Pharmacy, Anhui University of Chinese Medicine, Hefei 230012, Anhui China; 2.Traditional Chinese Medicine Resources Protection and Development, Anhui Academy of Chinese Medicine, Hefei 230012, Anhui China)
  • Received:2018-10-29 Revised:2018-12-02 Online:2019-03-30 Published:2019-03-30
  • Contact: XING Shi-hai

多花黄精诱导愈伤组织与不定芽培养基筛选

叶雨心,任梦婷,易伟豪,齐青,彭代银,邢世海   

  1. (1.安徽中医药大学药学院,安徽 合肥 230012;2.安徽省中医药科学院中药资源保护与开发研究所,安徽 合肥 230012)
  • 通讯作者: 邢世海
  • 作者简介:叶雨心,本科生,从事分子生药学研究。
  • 基金资助:
    安徽中医药大学科学研究基金重点项目(2018zrzd);国家人社部高层次留学人才回国资助和安徽省留学人员创新项目择优资助计划(邢世海)(DT18100035);安徽省教育厅高等学校自然科学研究项目“霍山石斛蛋白质组及蛋白质翻译后磷酸化修饰组学研究”;安徽省自然科学基金面上项目“青蒿素在黄花蒿体内特异合成分子机理的研究”(1908085MH268)

Abstract: Rootstocks of Polygonatum cyrtonema were used as explants, and the effects of different plant growth regulators and their combinations on the callus induction were studied by L9(34) orthogonal test. The well medium was screened for directly buds formation by organogenesis of this medicinal plant. The results showed that the effect of callus induction was remarkable in medium containing 2,4-D and KT. The optimum medium for callus induction was MS + 6-BA 2.0 mg·L-1 + 2,4-D 0.5 mg·L-1 + NAA 0.1 mg·L-1 + KT 1.0 mg·L-1, and the callus induction rate reached up to 39.10%. The medium of MS + 6-BA 4.0 mg·L-1 + NAA 0.2 mg·L-1 was optimal for inducing adventitious buds.

Key words: Polygonatum cyrtonema, callus, organogenesis, adventitious bud induction, plant growth regulator

摘要: 以多花黄精Polygonatum cyrtonema的根状茎为外植体,通过L9(34)正交试验比较不同植物生长调节剂及其组合对多花黄精愈伤组织诱导的影响,筛选最适生长调节剂配方,同时筛选通过器官发生方式直接成芽较为合适的培养基。结果表明,含有2,4-D和KT的培养基诱导愈伤组织效果显著,多花黄精愈伤组织诱导的最适培养基为MS + 6-BA 2.0 mg·L-1 + 2,4-D 0.5 mg·L-1 + NAA 0.1 mg·L-1 + KT 1.0 mg·L-1,该培养基的愈伤组织诱导率可达39.10%;培养基MS + 6-BA 4.0 mg·L-1 + NAA 0.2 mg·L-1可诱导多花黄精根状茎直接产生不定芽。

关键词: 多花黄精, 愈伤组织, 器官发生, 不定芽诱导, 植物生长调节剂

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