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无籽刺梨离体快繁技术研究

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采用无籽刺梨嫩枝茎段为外植体,MS为基本培养基,进行无籽刺梨组织培养研究,探讨了影响无籽刺梨组培快繁的主要因素,包括外植体的消毒;最佳激素浓度及组合;最佳生根培养基及组培苗的移栽等.结果表明:无籽刺梨茎段在0.1%升汞中处理12 min中消毒效果最佳,有效存活率达77.78%;腋芽诱导的最佳激素配比为6-BA 0.5 mg/L+ IBA 0.1 mg/L,诱导率为100%;去顶后芽的增殖最适培养基为MS+ 6-BA0.2 mg/L+ IBA 0.02 mg/L,增殖倍数可达3.22倍;在1/2 MS+IBA 0.3 mg/L的生根培养基上,不定芽生根率为100%,移栽后成活率在95%以上.
Study on in vitro Propagation of Rosa sterilis
The young stem was taken as the explants for studying on tissue culture of Rosa sterilis.The factors of tissue culture were studied,including the disinfection of explants,the selection of optimum consistency and combination of hormones,the selection of optimum culture medium combinations of root induction and the transplant of the tissue culture seedling.The results showed that the optimum explants sterilization time was dip in 0.1% HgCl2 for 12 min,and the effective survival rate was 77.78%.The suitable combination for the inducement of axillary buds was MS + 6-BA 0.5 mg/L + IBA 0.1 mg/L,and germination rate was 100%.Shoots cultured on the medium of MS + 6-BA 0.2 mg/L + IBA 0.02 mg/L could be multiplicated by 3.22 fold and above.The media formula for rooting was 1/2 MS + IBA 0.3 mg/L.In this media,the rootage rate was 100%,and the survival rate was 95% after transplanting.

Tissue culturein vitro propagationaxillary bud inducementmultiplicationrooting

唐军荣、郑元、张亚威、林源、李永和、辛培尧

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西南林业大学,国家林业局西南地区生物多样性保育重点实验室,云南昆明650224

中国环境科学研究院,北京100012

西南林业大学,云南生物多样性研究院,云南昆明650224

无籽刺梨 离体快繁 腋芽诱导 增殖 生根

云南省科技厅项目

2008PY021

2015

云南农业大学学报(自然科学)
云南农业大学

云南农业大学学报(自然科学)

CSTPCDCSCD北大核心
影响因子:0.828
ISSN:1004-390X
年,卷(期):2015.30(1)
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