Tissue culture method of hemerocallis middendorfii 'lace scarf'
A large-flowered Hemerocallis, tissue culture technology, applied in horticultural methods, botanical equipment and methods, horticulture and other directions, can solve the problems of low seed setting rate of Hemerocallis, limitation of large-scale promotion of new varieties of Hemerocallis, low quantity and high price, and achieves easy growth. bud effect
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Embodiment 1
[0028] The tissue culture method of Hemerocallis grandiflora "lace square scarf", the method comprises the following steps:
[0029] (1) The acquisition of sterile materials, the stem tip of Hemerocallis grandiflora "Lace Square" can be taken all year round, cleaned and cut into 3 small pieces of 1 cm, soaked in 4-5% Shannong No. 1 type I solution for 16 hours , add 1 / 4 salts of MS basic medium to the soaking solution, the MS basic medium adopts white sugar 20g / L, agar 5g / L, pH5.8, take it out and inoculate it on the callus induction medium, the callus induction medium is MS+ Shannong No. 1 Type II 0.1%+6—BA1.8mg / L+NAA0.3mg / L;
[0030] (2) Callus induction: under the conditions of 25±2°C, light intensity 1500Lx, and light 12h / d, obvious callus tissue can be seen at the shoot tip after 40 days, and cultured in dark for 20 days;
[0031] (3) Bud differentiation: connect the callus to the bud differentiation induction medium, the bud differentiation induction medium is MS+Shanno...
Embodiment 2
[0038] The tissue culture method of Hemerocallis grandiflora "lace square scarf", the method comprises the following steps:
[0039] (1) The acquisition of sterile materials, the stem tip of Hemerocallis grandiflora "Lace Square" can be taken all year round, cleaned and cut into 3 small pieces of 1 cm, soaked in 4-5% Shannong No. 1 type I solution for 16 hours , add 1 / 4 salts of MS basic medium to the soaking solution, the MS basic medium adopts white sugar 20g / L, agar 5g / L, pH5.8, take it out and inoculate it on the callus induction medium, the callus induction medium is MS+Shannong No. 1 Type II 0.1%+6—BA2.0mg / L+NAA0.5mg / L;
[0040] (2) Callus induction: under the conditions of 25±2°C, light intensity 2000Lx, and light 12h / d, obvious callus tissue can be seen at the shoot tip after 40 days, and cultured in dark for 25 days;
[0041] (3) Bud differentiation: connect the callus to the bud differentiation induction medium, the bud differentiation induction medium is MS+Shannon...
Embodiment 3
[0048] The tissue culture method of Hemerocallis grandiflora "lace square scarf", the method comprises the following steps:
[0049] (1) The acquisition of sterile materials, the stem tip of Hemerocallis grandiflora "Lace Square" can be taken all year round, cleaned and cut into 3 small pieces of 1 cm, soaked in 4-5% Shannong No. 1 type I solution for 16 hours , add 1 / 4 salts of MS basic medium to the soaking solution, the MS basic medium adopts white sugar 20g / L, agar 5g / L, pH5.8, take it out and inoculate it on the callus induction medium, the callus induction medium is MS+Shannong No. 1 Type II 0.1%+6—BA2.3mg / L+NAA0.6mg / L;
[0050] (2) Callus induction: under the conditions of 25±2°C, light intensity 2500Lx, and light 12h / d, obvious callus tissue can be seen at the shoot tip after 40 days, and cultured in dark for 30 days;
[0051] (3) Bud differentiation: connect the callus to the bud differentiation induction medium, the bud differentiation induction medium is MS+Shannon...
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