Cultivation method of test-tube strong seedlings of natural lingonberry in Daxing'an Mountains
A technology of lingonberries and cultivation methods, applied in horticultural methods, botany equipment and methods, horticulture, etc., can solve the problems of slender test-tube seedlings, difficult rooting and transplanting, weak growth potential, etc., to reduce production waste, reduce Production cost and the effect of improving the effective utilization rate
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specific Embodiment approach 1
[0012] Specific implementation mode one: the cultivation method of the natural Dusi lingonberry test tube strong seedlings in Daxing'an Mountains in this embodiment is specifically carried out according to the following steps:
[0013] 1. Induction culture: Using the axillary buds of the natural Vaccinium vaccinium in Daxing’an Mountains as explants, the axillary buds of Vaccinium vaccinium were sterilized by conventional tissue culture and then transferred to the induction medium in the ultra-clean workbench for induction culture for 18 days~ 22d, obtain the axillary bud after induction culture;
[0014] 2. Differentiation culture: transfer the axillary buds after the induction culture obtained in step 1 to the differentiation medium and carry out differentiation culture for 50d to 70d to obtain thin and weak seedlings of Vaccinium vaccinium; the average height of the vaccinium vaccinium seedlings is 6cm;
[0015] 3. Cultivation of strong seedlings: pour the strong seedling m...
specific Embodiment approach 2
[0017] Specific embodiment 2: The difference between this embodiment and specific embodiment 1 is that the routine tissue culture disinfection described in step 1 is to rinse the axillary buds of Vaccinium cranberry with running water for 10 minutes, and then add 0.1% HgCl to the ultra-clean workbench. 2 Fully soak and disinfect for 2.5 minutes, then rinse with sterile water for 3 times, soak in sterile water for 40 minutes, take out, and use sterile filter paper to dry the surface moisture of the material. Others are the same as the first embodiment.
specific Embodiment approach 3
[0018] Specific embodiment three: the difference between this embodiment and specific embodiment one or two is: the induction medium described in step one is: DY basic medium + zeatin 0.5mg / L + sucrose 25g / L ~ 35g / L + strength of 1400g / cm 2 Agar 6.0g / L~7.0g / L, pH value 5.5~6.0;
[0019] KNO in the DY basic medium 3 The content is 180mg / L~200mg / L, NH 4 NO 3 The content is 400mg / L~410mg / L, MgSO 4 ·7H 2 O content is 365mg / L~380mg / L, KH 2 PO 4 The content is 160mg / L~180mg / L, Ca(NO 3 ) 2 4H 2 O content is 680mg / L~690mg / L, H 3 BO 3 The content is 6.3mg / L, MnSO 4 4H 2 O content is 22.4mg / L, ZnSO 4 ·7H 2 O content is 8.5mg / L, Na 2 MoO 4 2H 2 O content is 0.24mg / L, CuSO 4 ·5H 2 O content is 0.24mg / L, C 10 h 13 FeN 2 NaO 8 The content is 73mg / L~74mg / L, Na 2 The content of EDTA is 37mg / L~38mg / L, the content of thiamine hydrochloride is 0.05mg / L~0.15mg / L, the content of niacin is 0.45mg / L~0.55mg / L, the content of pyridoxine hydrochloride 0.5mg / L~0.6mg / L, the cont...
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