Rapid breeding method of senecio cruentus
A cineraria, fast technology, applied in the field of plant tissue culture, can solve the problems of unfavorable in vitro tissue regeneration large-scale culture, low germination rate of somatic embryos, poor stability of regeneration system, etc. The effect of high planting survival rate and stable regeneration system
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Embodiment 1
[0050] 1. Test materials
[0051] 1. Mature cineraria ‘clown’ seeds come from the US Gold Smith company.
[0052] The five color varieties of Cineraria'clown' used in the embodiment of the present invention are blue, white, pink, scarlet and yellow.
[0053] 2. Plant growth regulator
[0054] The plant growth regulators used in the present invention adopt domestic indole butyric acid (IBA), naphthaleneacetic acid (NAA), 6-benzylamino adenine (6-BA) and 2,4-dichlorophenoxyacetic acid (2 , 4-D).
[0055] 3. Preparation of culture medium:
[0056] (1) The composition or preparation method of "MS basic medium";
[0057] Table 1 MS medium (Murashige and Skoog, 1962)
[0058] MS large elements
Mother liquor composition
content
(g / L)
MS trace elements
Mother liquor composition
content
(g / L)
Mother liquor composition
content
(g / L)
NH4NO3
33
H 3 BO 3
1.24
20
KNO 3
38
ZnSO 4 ·7H 2 O
1.72
0.1
CaCl 2 ·2H 2 O
8.8
MnSO 4 ·4H ...
Embodiment 2
[0093] In addition to aseptic seedling culture, the seeds of scarlet cineraria "clown" were used; the 6-BA used in the clumping bud induction medium was 0.5 mg / L and the NAA was 0 mg / L; the 6-BA used in the callus induction medium was 2.0mg / L, NAA is 3.0mg / L, 2,4-D is 0.5mg / L; 6-BA used in callus proliferation medium is 0.5mg / L, NAA is 0.5mg / L; adventitious bud differentiation The 6-BA used in the medium is 2.0 mg / L, NAA is 3.0 mg / L, and 2,4-D is 0.5 mg / L; the IBA used in the adventitious rooting medium is 0.1 mg / L, all others are the same Example 1 is the same.
Embodiment 3
[0095] In addition to aseptic seedling culture, the seeds of blue cineraria "clown" are used; the 6-BA used in the clumping bud induction medium is 1.0 mg / L and the NAA is 0.1 mg / L; the 6-BA used in the callus induction medium 3.0mg / L, NAA 2.0mg / L, 2,4-D 0.5mg / L; 6-BA used in callus proliferation medium is 1.0mg / L, NAA is 0.5mg / L; adventitious buds The differentiation medium used 6-BA is 3.0mg / L, NAA is 2.0mg / L, 2,4-D is 0.5mg / L; the adventitious rooting medium used NAA is 0.1mg / L, the others are the same Example 1 is the same.
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