• 中文核心期刊
  • CSCD来源期刊
  • 中国科技核心期刊
  • CA、CABI、ZR收录期刊

山药组培快繁技术条件的优化

Optimization of Technical Conditions for Tissue Culture and Rapid Propagation of Chinese Yam

  • 摘要: 以‘明淮2号’山药为试验材料,进行山药快繁技术条件的优化研究。结果表明:初代培养的外植体以中部带芽茎段为好。最好的消毒方法是用70%的酒精浸泡10s,0.1%HgCl2浸泡10 min,污染率为15.0%,死亡率为6.7%。初代培养基为:MS+6-BA1.0 mg·L-1+NAA0.05 mg·L-1+PVP100 mg·L-1+VC 500 mg·L-1+AC0.5 g·L-1+蔗糖30 g·L-1,2周后转入相同配方的固体培养基中,褐化率为36.7%,诱导率为81.7%。增殖培养基为:MS+6-BA2.0 mg·L-1+KT1.0 mg·L-1+NAA0.05 mg·L-1+PP333 0.05 mg·L-1+琼脂粉4.0 g·L-1+蔗糖30 g·L-1,30 d后增殖系数为2.97。生根培养基为:1/2MS+NAA0.3 mg·L-1+IBA0.2 mg·L-1+AC1.0 g·L-1+琼脂粉4.5 g·L-1+蔗糖20 g·L-1,30 d生根率达91.3%。组培苗炼苗2周,取出用多菌灵浸泡后移栽到草炭土穴盘中,成活率达70%以上。

     

    Abstract: With'Ming Huai yam 2' as the experimental material, we optimized the technological conditions of the rapid propagation of yam. The results showed that in vitro culture, the best explant was segment with bud in middle part of new shoot. The best disinfection method was with 70% alcohol immersion 10 s, and 0.1% HgCl2 for 10 min, the pollution rate of which was 15.0%, and the mortality rate was 6.7%. The primary culture medium was:MS+6-BA 1.0 mg+NAA 0.05 mg·L-1+PVP 100 mg·L-1+VC 500 mg·L-1 +AC 0.5 g·L-1+Sug 30 g·L-1. After two weeks, it was transferred to the solid medium with the same formula. The browning rate was 36.7% and the induction rate was 81.7%. The subculture multiplication medium was:MS+6-BA 2.0 mg·L-1+KT 1.0 mg·L-1+NAA 0.05 mg·L-1+PP333 0.05 mg·L-1+Agar 4.0 g·L-1+Sug 30 g·L-1. The proliferation coefficient of 30 d was 2.97. The rooting medium was:1/2MS+NAA 0.3 mg·L-1+IBA 0.2 mg·L-1+AC 1.0 g·L-1+Agar 4.5 g·L-1+Sug 20 g·L-1. The rooting rate was 91.3%. After two weeks of acclimation in the greenhouse, the plants were soaked with carbendazim and cooled to dry, then transplanted to peat soil tray. The transplanting survival rate was more than 70%.

     

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