Establishment method of achnatherum inebrians mature embryo callus induction and regeneration system
A technology of callus induction and establishment method, which is applied in the direction of plant regeneration, horticultural methods, botany equipment and methods, etc., and achieves the effect of simple operation and low cost
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Embodiment 1
[0057] Method concrete steps of the present invention are as follows:
[0058] (1) Selection and treatment of plant materials: Select mature seeds of Drunken Horseweed with uniform color and size, remove the lemma and rinse under running water for 30 minutes, then treat with 45% alcohol for 5 minutes, rinse with sterile water 2-3 times, and use Disinfect with 10% sodium hypochlorite for 10 minutes, rinse with sterile water for 3-5 times, place the seeds on sterile filter paper until the seeds are dry and ready for use; the seeds of Drunken Horse Grass refer to: wild Drunken Horse collected in Xiahe grass seeds.
[0059] (2) The formulations of induction medium, differentiation proliferation medium and rooting medium are as follows:
[0060] The basal medium was MS medium plus 30 g sucrose L -1 and agar 10 g·L -1 ;
[0061] Induction medium and differentiation and proliferation medium were supplemented with different treatment hormones as basal medium.
[0062] The callus ...
Embodiment 2
[0069] The difference between this embodiment and embodiment 1 is:
[0070] The selected Drunken Horse Grass seeds were collected from Tianzhu.
[0071] The basal medium was MS medium plus 30 g sucrose L -1 and agar 10 g·L -1 ;
[0072] The callus induction medium is: basal medium + 0.5 mg·L -1 6-BA+3.0 mg·L -1 2,4-D, the induction rate is 96%;
[0073] The proliferation medium is: basal medium+3.0mg / L6-BA+0.1mg / L NAA, the proliferation rate is 83%;
[0074] The rooting medium is: 1 / 2 basal medium+0.2 mg / L NAA, and the rooting rate is 100%.
Embodiment 3
[0076] The difference between this embodiment and embodiment 1 is:
[0077] The selected seeds of Drunken Horse Grass are the seeds of Drunken Horse Grass collected in Xinjiang.
[0078] The basal medium was MS medium plus 30 g sucrose L -1 and agar 10 g·L -1 ;
[0079] The callus induction medium is: basal medium + 0.5 mg·L -1 6-BA+1.0mg·L -1 2,4-D, the induction rate is 95%;
[0080] The proliferation medium is: basal medium+1.5mg / L6-BA+0.2mg / L NAA, the proliferation rate is 88%;
[0081] The rooting medium is: 1 / 2 basal medium + 0.4 mg / L NAA, and the rooting rate is 100%.
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