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雪菊的组织培养研究
引用本文:唐建卓,秦勇,叶尔根·夏依木拉提,古宁宁.雪菊的组织培养研究[J].新疆农业大学学报,2013(6):454-457.
作者姓名:唐建卓  秦勇  叶尔根·夏依木拉提  古宁宁
作者单位:新疆农业大学林学与园艺学院,乌鲁木齐530052
基金项目:国家自然科学基金项目(31360319)
摘    要:以雪菊带芽茎段、茎尖、叶片为外植体以MS为培养基添加不同浓度6BA和NAA进行组织培养实验,结果表明适合带芽茎段愈伤组织诱导的培养基为MS+6BA1.0mg/L+XAA0.3mg/L;适合茎尖愈伤组织诱导的培养基为MS+6BA1.0mg/L+XAA0.1mg/L;适合叶片愈伤组织诱导的培养基为MS+6BA3.0mg/L+NAA0.3mg/L,适合雪菊愈伤组织增殖和不定芽诱导的培养基为MS+6BA2.0mg/L+NAA0.3mg/L;适合雪菊试管苗生根的培养基为1/2MS+6BA0.3mg/L+XAA0.03mg/L,蔗糖减半,以雪菊无菌苗的带芽茎段、茎尖和叶片为外植体成功地诱导出了愈伤组织,其中带芽茎段愈伤组织诱导率最高时间最短效果最好茎尖次之叶片最差.

关 键 词:雪菊  组织培养  愈伤组织

Research on Tissue Culture of Coreopsis tinctoria Nutt.
TANG Jian-Zhuo,QIN Yong,Yeergen Shannonmulati,GU Ning-Ning.Research on Tissue Culture of Coreopsis tinctoria Nutt.[J].Journal of Xinjiang Agricultural University,2013(6):454-457.
Authors:TANG Jian-Zhuo  QIN Yong  Yeergen Shannonmulati  GU Ning-Ning
Affiliation:(College of Forestry and Hort icult ure , Xinjiang Agricult ural University, Urumqi 830052, China)
Abstract:The experiment of tis sure culture was designed to use Coreopsis tinctoria wi th bud stern section, stern tip and leaf as explant and to use MS as medium, adding 6-BA and NAA with different concentration. The result showed that the medium suitable for bud stern section callus induction was MS+6-BA1. 0 mg/L+NAA 0.3 mg!L;The medium suitable for stern tip callus induction was MS+6-BA 1.0 mg/L+NAA 0.1 mg/L; The medium suitable for leaf callus induction was MS+6-BA 3.0 mg/L+ NAA0.3 mg/L; The medium suitable for callus proliferation and adventitious bud induction was MS+6-BA 2.0 mg/L+NAA 0.3 mg!L; The medium suita hle for tube seedling rooting was 1/2MS + 6-BA0. 3mg/L + NAA 0.03 mg/L and sucrose in half was suitable for Coreopsis tinctoria tube seedling rooting culture. The bud stern section vstern tip and leaf with st erit ity seedling of Coreopsis tinctoria were used as explant s , the callus was successfully induced-among which the bud stern section callus had the highest callus induction rate with the shortest tim evhest effect, but stern tip s leaf were the worst.
Keywords:Coreo psis tinctoria  tissue culture  call us
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