Vaccinium tissue rapid propagation medium and its cultivation method
A medium and inducing medium technology, applied in the field of plant tissue culture, can solve the problems of poor in vitro rapid propagation effect and the like, and achieve the effect of shortening the process of popularization of improved varieties
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specific Embodiment approach 1
[0032] Specific embodiment 1: In this embodiment, the rapid propagation medium of European lingonberry tissue includes two kinds of culture medium: axillary bud induction medium and differentiation and proliferation medium; wherein, the described axillary bud induction medium contains 0.1mg / L~1.0mg / L Dy medium of L zeatin;
[0033] The differentiation and proliferation medium is Dy medium containing 0.1mg / L~1.0mg / L 6-benzylaminopurine and 0.1mg / L~1.0mg / L zeatin;
[0034] Wherein, the Dy medium is composed of macroelements, calcium salts, trace elements, iron complex salts, organic substances, and the strength is 1400g / cm 2 of agar and distilled water;
[0035] Each 1L of Dy medium contains the above-mentioned macroelements ranging from 180mg / L to 200mg / L of KNO 3 , 400mg / L~410mg / L NH 4 NO 3 , 365mg / L~380mg / L of MgSO 4 ·7H 2 O and 160mg / L~180mg / L of KH 2 PO 4 composition;
[0036] Every 1L of Dy medium contains said calcium salt as Ca(NO) of 680mg / L~690mg / L 3 ) 2 4H ...
specific Embodiment approach 2
[0041] Embodiment 2: This embodiment differs from Embodiment 1 in that: the axillary bud induction medium is Dy medium containing 0.6 mg / L zeatin. Others are the same as the first embodiment.
specific Embodiment approach 3
[0042] Specific embodiment three: the difference between this embodiment and specific embodiment one or two is that: the differentiation and proliferation medium is Dy medium containing 0.5 mg / L 6-benzylaminopurine and 1.0 mg / L zeatin . Others are the same as those in Embodiment 1 or 2.
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