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CULTURE MEDIUM FOR IMPROVING INDUCTION RATE OF TISSUE CULTURED PLANT, PREPARATION METHOD, AND APPLICATION

机译:提高组织培养植物诱导率的培养基,制备方法和应用

摘要

Disclosed in the present invention are a culture medium for improving the induction rate of a tissue cultured plant, a preparation method, and an application. The culture medium comprises: 68-94 parts of WPM medium, 0.05-0.5 parts of zeatin, 0.1-1.5 parts of indole-3-acetic acid, 0.3-1.8 parts of brassinolide, 23-56 parts of sucrose, 2-6 parts of flavonoid, 6-18 parts of calcium phosphate, and 32-68 parts of sodium dodecylbenzenesulfonate. The preparation method comprises: mixing and dissolving the raw materials according to the amounts, adjusting the pH value to 5.4-5.6, and performing sterilization for 15-30 min. The culture medium is used for primary culture of Plumbago auriculata. The culture medium provided by the present invention can effectively improve the induction rate of plants to reach about 95%, and can improve the vigorous degree of subsequently cultured plantlets and improve the survival rate and adaptability thereof; moreover, the preparation method is simple, environment-friendly, and safe; in addition, the culture medium is applied to primary culture of Plumbago auriculata, effectively improving the induction rate and enabling Plumbago auriculata to grow vigorously.
机译:本发明公开了一种用于提高组织培养植物的诱导率的培养基,其制备方法和应用。培养基包括:68-94份WPM培养基,0.05-0.5份玉米素,0.1-1.5份吲哚-3-乙酸,0.3-1.8份油菜素内酯,23-56份蔗糖,2-6份黄酮,6-18份磷酸钙和32-68份十二烷基苯磺酸钠。制备方法是:根据原料量混合溶解,调节pH值至5.4-5.6,灭菌15-30分钟。该培养基用于白花石墨的原代培养。本发明提供的培养基可以有效地提高植物的诱导率达到95%左右,并且可以提高随后培养的幼苗的活力,提高其成活率和适应性。而且制备方法简单,环保,安全。此外,该培养基应用于白花石墨的原代培养中,有效提高了诱导率,并使白花石墨有力地生长。

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