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农学学报

农学学报 ›› 2012, Vol. 2 ›› Issue (8): 8-12.

• 农艺科学 作物遗传育种 生理生化 • 上一篇    下一篇

温莎甜荞再生体系建立的研究

闫超敏   

  • 收稿日期:2012-02-23 修回日期:2012-05-03 出版日期:2012-08-20 发布日期:2012-08-20

Research on the Regeneration System Establishment of Windsor Sweet Buckwheat

  • Received:2012-02-23 Revised:2012-05-03 Online:2012-08-20 Published:2012-08-20

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摘要：

为了荞麦的进一步研究和转基因体系的建立以及农杆菌介导转化的研究奠定基础，为基因工程改良荞麦芦丁生物合成提供了理论依据及技术保证。以温莎甜荞为研究材料，建立组织培养再生体系，以子叶和下胚轴为外植体，基本培养基为MS，添加不同浓度的生长素和细胞分裂素，设计不同激素配比组合，在相同的培养条件下，研究温莎甜荞子叶和下胚轴愈伤组织诱导和生长特征，筛选出诱导温莎甜荞愈伤组织的最适培养基，为基因工程提供参考和理论依据。研究表明：温莎甜荞子叶产生愈伤组织的最佳培养基为MS+2,4-D 2 mg/L+6-BA 0.4 mg/L。诱导芽的最佳培养基为MS+6-BA 1.5 mg/L+IBA 0.3 mg/L。下胚轴诱导愈伤组织的最佳培养基为MS+2,4-D 3 mg/L+6-BA 0.1 mg/L。诱导芽的最佳培养基为MS+6-BA 3 mg/L+IBA 0.5 mg/L。生根的最佳培养基为1/2 MS。

关键词: 动力学方程, 动力学方程, 营养生长期, 生殖生长期, Forcal, Matlab

Abstract:

The research as the transgene system establishment, the agricultural bacillus lesds transformed the research to lay the foundtion which has further provided the theory basis and the technical guarantee for the genetic engineering improvement of the buckwheat biosynthesis. Selecting the buckwheat which is windsor sweet buckwheat for establishing regeneration system and antibitic screening system, We know explants are cotyledon and hypocotyl. The basic culture medium is called MS. We can add into the different Auxin and cytokinin under the different condition Auxin and cytokinin under the different condition, we studied Jiujiang bitter buckwheat of the seed leaf and under the hypocotyl injuries the organization the induction as well as does not decide the bud differentiation and the growth situation we can establish the best regeneration system through researching the different explants, as the transgene system establishment has further provided the theory basis. The research indicated that The windsor sweet buckwheat seed leaf produces injuries the organization the best culture medium is MS + 2,4-D 2 mg/L + 6-BA 0.4 mg/L. The induction bud's best culture medium is MS + 6-BA 1.5 mg/L + IBA 0.3 mg/l.The next hypocotyl induction injuries the organization the best culture medium is MS + 2,4-D 3 mg/L + 6-BA 0.5 mg/l, the induction bud's best culture medium is MS + 6-BA 0.05 mg/L + IBA 0.1 mg/L. The rooting induction the best culture medium is 1/2 MS.