首页> 外国专利> METHOD FOR CULTURING PUERARIA THOMSONII BY PROLIFERATION OF SINGLE-BUD STEM SEGMENT AND ONE-STEP SEEDLING FORMATION

METHOD FOR CULTURING PUERARIA THOMSONII BY PROLIFERATION OF SINGLE-BUD STEM SEGMENT AND ONE-STEP SEEDLING FORMATION

机译:单芽茎段和一步幼苗形成培养Pueraria ThomsonII的方法

摘要

Disclosed is a method for culturing Pueraria thomsonii by proliferation of a single-bud stem segment and one-step seedling formation. The method specifically comprises the following steps: S1, explant treatment: selecting a tender vine that grows well and has no diseases or insect pests, immersing and disinfecting same, and then washing the vine with sterile water; finally, absorbing moisture on the surface of a stem segment for later use by means of using sterile filter paper; S2, culture of a sterile seedling: under sterile conditions, cutting the vine treated in step S1 into a stem segment with a bud; vertically inserting a biological lower end into a primary culture medium for culture, so as to obtain the sterile seedling; S3: proliferation and rooting induction of the single-bud stem segment: under sterile conditions, cutting the sterile seedling obtained in step S2 to obtain a single-bud stem segment with an axillary bud, and transferring the single-bud stem segment into an intermittent submerged culture device for multiplication and rooting culture; S4, transplanting and survival of a tissue culture seedling: transferring a sterile bottle seedling that is 3-4 cm high, grows well, and has well developed roots from a culture room to a greenhouse for seedling hardening; and then, taking out the seedling, washing away a liquid culture medium attached to the seedling, and planting the seedling in a nutrition pot.
机译:公开了一种通过单芽茎链段和一步幼苗形成培养Pueraria Thomsonii的方法。该方法具体包括以下步骤:S1,外植治疗:选择柔软的葡萄浓郁,浓郁,没有疾病或虫害,浸入和消毒相同,然后用无菌水洗涤藤蔓;最后,通过使用无菌滤纸吸收茎段表面上的水分; S2,无菌幼苗的培养:在无菌条件下,将步骤S1中处理的藤切割成芽的茎段;将生物下端垂直插入培养的初级培养基中,以获得无菌幼苗; S3:单芽茎段的增殖和生根诱导:在无菌条件下,切割在步骤S2中获得的无菌幼苗,得到具有腋芽的单芽茎段,并将单芽茎段转移到间歇淹没培养装置,用于繁殖和生根培养;组织培养幼苗的移植和存活:转移3-4厘米高,井的无菌瓶幼苗,从培养室到一个温室的幼苗硬化产生良好的根;然后,取出幼苗,洗掉附着在幼苗上的液体培养基,并在营养罐中种植幼苗。

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