Spathiphyllum tetraploid inducing method
A technology of tetraploid and white crane, which is applied in the field of induction of tetraploid of white crane, can solve the problem of not inducing polyploid of white crane, and achieve the effects of easy proliferation and differentiation, good repeatability, and shortened preparation time
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Embodiment 1
[0077] step one:
[0078] Select the diploid white crane taro variety "Xiangxiang Baizhang" that grows vigorously, has emerald green leaves, plant height of 2-2.5cm, and is not excessively long and not jointed.
[0079] Step two:
[0080] The stem tip buds of robust tissue cultured plantlets were cut, inoculated in a solid induction medium with a pH value of 5.6 to 5.8, and cultivated for 32 days to obtain callus with buds of tissue cultured plantlets;
[0081] Among them, the formula of solid induction medium is: MS basic medium, 6-benzylaminoadenine (6-BA) 1.0 mg / L, 2,4-D 0.3mg / L, sugar 30g / L, agar 5g / L .
[0082] Step three:
[0083] The callus was inoculated in a solid differentiation medium with a pH value of 5.6 to 5.8, pre-cultured for 5 days, then inoculated in a liquid differentiation medium with a pH value of 5.6 to 5.8 and immersed for 8 days, and in the liquid differentiation medium Shake well every 2 days during the culture period;
[0084] Among them, the fo...
Embodiment 2
[0105] step one:
[0106] Select the diploid white crane taro variety "Meijiu", which grows vigorously, has emerald green leaves, and has a plant height of 1.8-2.2 cm. It is not excessively long and does not joint.
[0107] Step two:
[0108] The stem tip buds of robust tissue cultured plantlets were cut, inoculated in a solid induction medium with a pH value of 5.6 to 5.8, and cultivated for 36 days to obtain callus of tissue cultured plantlets with buds;
[0109] Among them, the formula of the solid induction medium is: MS basic medium, 6-benzylaminoadenine (6-BA) 1.1mg / L, 2,4-D 0.4mg / L, sugar 30g / L, agar 5g / L .
[0110] Step three:
[0111] The callus was inoculated in a solid differentiation medium with a pH value of 5.6 to 5.8, pre-cultured for 6 days, then inoculated in a liquid differentiation medium with a pH value of 5.6 to 5.8 and immersed for 9 days, and in the liquid differentiation medium Shake well every 2 days during the culture period;
[0112] Among them,...
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