| 大岩桐组织培养与快繁技术研究 |
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| 引用本文： | 唐伟斌,刘占牛.大岩桐组织培养与快繁技术研究[J].安徽农业科学,2005,33(8):1418-1418. |
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| 作者姓名： | 唐伟斌 刘占牛 |
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| 作者单位： | 邢台学院生物系,河北,邢台,054001;邢台学院生物系,河北,邢台,054001 |
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| 摘 要： | 大岩桐(Sinningiaspeciosa)幼嫩叶片可诱导形成愈伤组织及再生小植株。最适宜的愈伤组织诱导培养基为MS+6!BA1.5mg/L+NAA0.2mg/L;分化继代培养基为MS+6!BA1.0mg/L+NAA0.1mg/L;生根培养基为1/2MS+IBA0.2mg/L。
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| 关 键 词： | 大岩桐 组织培养 快繁 |
| 文章编号： | 0517-6611（2005）08-1418-01 |
| 收稿时间： | 05 26 2005 12:00AM |
| 修稿时间： | 2005-05-26 |
Study on Rapid Propagation and Tissue Culture of Sinningia speciosa |
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| Tang WeiBin;Liu ZhanNiu.Study on Rapid Propagation and Tissue Culture of Sinningia speciosa[J].Journal of Anhui Agricultural Sciences,2005,33(8):1418-1418. |
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| Authors: | Tang WeiBin;Liu ZhanNiu |
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| Abstract: | The leaves of Sinningia speciosa as the explants was studied for the tube propagation. The results indicated that the leaves couldinduce callus. The most appropriate media in culture stages were:①MS + 6-BA 1.5 mg/L + NAA 0.2 mg/L for the formation of callus; ②MS + 6-BA1.0 mg/L+ NAA0.1 mg/Lfor producingauxiliarybuds; ③1/2MS+ IBA0.2 mg/Lfor rooting. |
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| Keywords: | Sinningia speciose Tissue culture Rapid propagation |
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