Subtropical Plant Science ›› 2020, Vol. 49 ›› Issue (02): 145-147.DOI: 10.3969/j.issn.1009-7791.2020.01.012

• Tissue culture • Previous Articles     Next Articles

In vitro Culture and Rapid Propagation of Hypoxis angustifolia

LI Hong-lin, ZHONG Zhi-xiang, XIE Juan, HU Guang-wan   

  1. (Wuhan Botanical Garden, Chinese Academy of Sciences, Wuhan 430074, Hubei China)
  • Received:2019-08-29 Revised:2019-11-06 Online:2020-04-30 Published:2020-04-30
  • Contact: HU Guang-wan

狭叶小金梅草组织培养与快速繁殖

李洪林,钟志祥,谢 娟,胡光万   

  1. (中国科学院武汉植物园,湖北 武汉 430074)
  • 通讯作者: 胡光万
  • 基金资助:
    中国科学院中-非联合研究中心项目(SAJC201614)资助

Abstract: The buds of Hypoxis angustifolia were used as material for tissue culturing. The results showed that the optimum culture medium for bud callus induction was MS + 6-BA 0.8 mg·L-1 + NAA 0.05 mg·L-1 + TDZ 0.1 mg·L-1; the culture medium for bud induction was MS + 6-BA 0.5 mg·L-1 + NAA 0.02 mg·L-1 + AC 0.2 g·L-1; the culture medium for propagation was MS + 6-BA 1.0 mg·L-1 + NAA 0.1 mg·L-1 + Huabao-1 1 g·L-1 + AC 0.2 g·L-1. And the subculture circle was 30 d, the multiplication rate was 10-20. The culture medium for root was 1/2 MS + IBA 0.5 mg·L-1 + NAA 0.02 mg·L-1 +AC 0.5 g·L-1. The suitable transplanting medium was surface soil and vermiculite (3:1), the survival rate reached 80%.

Key words: Hypoxis angustifolia, bud, propagation, tissue culture

摘要: 以狭叶小金梅草(Hypoxis angustifolia)当年花苞为材料进行离体快速繁殖体系研究。结果表明,花苞的愈伤诱导适宜培养基为MS + 6-BA 0.8 mg·L-1 + NAA 0.05 mg·L-1 + TDZ 0.1 mg·L-1;诱导芽培养基为MS + 6-BA 0.5 mg·L-1 + NAA 0.02 mg·L-1 + AC(活性碳) 0.2 g·L-1;芽继代增殖培养基为MS + 6-BA 1.0 mg·L-1+ NAA 0.1 mg·L-1 + 花宝1号1 g·L-1 + AC 0.2 g·L-1,30 d为一个继代周期,增殖系数达10~20倍;壮苗生根培养基为1/2MS + IBA 0.5 mg·L-1 + NAA 0.02 mg·L-1 + AC 0.5 g·L-1。将生根苗移栽至泥土:蛭石按3:1配制旳基质中,盖膜保湿,成活率达80%。

关键词: 狭叶小金梅草, 花蕾, 增殖, 离体培养

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