王亚楠, 张湛仪, 赵李姗, 余俊玲, 汪梦婷, 蔡年辉, 唐军荣, 许玉兰. 紫果西番莲愈伤组织诱导分化及不定芽增殖研究[J]. 西南林业大学学报, 2019, 39(3): 155-160. DOI: 10.11929/j.swfu.201903130
引用本文: 王亚楠, 张湛仪, 赵李姗, 余俊玲, 汪梦婷, 蔡年辉, 唐军荣, 许玉兰. 紫果西番莲愈伤组织诱导分化及不定芽增殖研究[J]. 西南林业大学学报, 2019, 39(3): 155-160. DOI: 10.11929/j.swfu.201903130
Yanan Wang, Zhanyi Zhang, Lishan Zhao, Junling Yu, Mengting Wang, Nianhui Cai, Junrong Tang, Yulan Xu. Induction and Differentiation of Callus and Propagation of Adventitious Buds in Passiflora caerulea[J]. Journal of Southwest Forestry University, 2019, 39(3): 155-160. DOI: 10.11929/j.swfu.201903130
Citation: Yanan Wang, Zhanyi Zhang, Lishan Zhao, Junling Yu, Mengting Wang, Nianhui Cai, Junrong Tang, Yulan Xu. Induction and Differentiation of Callus and Propagation of Adventitious Buds in Passiflora caerulea[J]. Journal of Southwest Forestry University, 2019, 39(3): 155-160. DOI: 10.11929/j.swfu.201903130

紫果西番莲愈伤组织诱导分化及不定芽增殖研究

Induction and Differentiation of Callus and Propagation of Adventitious Buds in Passiflora caerulea

  • 摘要: 以紫果西番莲离体培养的子叶为实验材料,对其愈伤组织进行诱导、分化及不定芽增殖。结果表明:在愈伤组织诱导中,以MS培养基+2,4-D 1.0 mg/L+TDZ 0.5 mg/L+琼脂3.8 g/L+蔗糖30 g/L的诱导效果最好,其诱导率为73.33%。在愈伤组织不定芽诱导中,以MS培养基+2,4-D 0.5 mg/L+TDZ 2.0 mg/L+琼脂3.8 g/L+蔗糖30 g/L的诱导率最佳,为46.67%。对不定芽继续进行增殖培养,以MS培养基+6-BA 1.0 mg/L+IAA 0.3 mg/L+琼脂4.0 g/L+蔗糖30 g/L最佳,增殖倍数为2.97。从而建立了西番莲植株再生体系,可进行优良材料的离体快繁。

     

    Abstract: Cotyledons of Passiflora caerulea were used as experimental materials to induce callus, differentiation and adventitious buds proliferation. The results showed that the callus induction medium using MS+2,4-D 1.0 mg/L+TDZ 0.5 mg/L+Agar 3.8 g/L+Sucrose 30 g/L had the highest rate of callus induction, and the induction rate was 73.33%. The optimum medium for inducing buds was MS+2,4-D 0.5 mg/L+TDZ 2.0 mg/L+Agar 3.8 g/L+Sucrose 30 g/L, the induction rate reached 46.67%.The optimum medium for further culturing adventitious buds was MS medium+6-BA 1.0 mg/L+IAA 0.3 mg/L+Agar 4.0 g/L+Sucrose 30 g/L, the multiplication multiple was 2.97. The established plant regeneration system could provide technical support for rapid propagation in vitro, ploidy breeding and genetic transformation of P. caerulea.

     

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