A method of propagating Paeoniae officinalis by tissue culture technique
A tissue culture and peony technology is applied in the field of propagating peony by inducing tissue culture seedlings to produce a bud tray structure by using tissue culture technology, and can solve the problems of affecting the transplanting of peony in vitro seedlings, restricting the development process of peony, weak growth potential of tissue culture seedlings, and the like, Achieve the effect of being conducive to large-scale production, less vitrification, and greater root vigor
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Embodiment 1
[0047] A method of utilizing tissue culture technology to propagate Radix Paeoniae Alba, comprising the steps of:
[0048] 1) Sterilization of peony explants: From January to February, collect the underground scale buds of peony as explants (see figure 1 ), cleaning, and sterilization (specifically: first rinse with tap water, then scrub the scales with detergent, and finally rinse with running water for 30 minutes; take it to the ultra-clean workbench for sterilization, with a volume concentration of 75% alcohol Sterilize for 30 seconds with 0.1% HgCl 2 Sterilize for 10 minutes, rinse with sterile water once, change to a sterile bottle, and then use HgCl with a mass concentration of 0.1% 2 Sterilize for 8 minutes, rinse with sterile water 3 to 4 times, and finally rinse with 250 mg / L cephalosporin sterile water once);
[0049] 2) Germination of peony explants: place the sterilized scale buds on sterile filter paper to absorb the water, peel off the peripheral scales with st...
Embodiment 2
[0058] The difference test of the culture effect brought by different medium composition is given below.
[0059] 1. Screening of explant germination medium
[0060] Insert the sterilized peonies stem tips into the explant germination medium, place them in the culture room for cultivation, the cultivation temperature is 23±2°C, the light intensity is 2000-3000Lx, and the light time is 12 hours / day. The explant germination medium uses MS medium as the basic medium, in which the macroelements are halved, that is, 1 / 2 MS medium, 30 g / L of sucrose and 6 g / L of agar are added, and different types and concentrations of plant growth are added at the same time. Regulate substances (see Table 1 for details), observe their effects on the germination of peony explants, count the germination rate 40 days after grafting and transfer, enter the latent bud induction link, germination rate = number of plants with germinated leaves / no pollution in this treatment The total number of plants * 1...
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