In vitro conservation method of oriental hybrid lily germ plasm resource
An in vitro preservation and germplasm technology, applied in horticultural methods, plant preservation, botanical equipment and methods, etc., can solve the problems of easy differentiation of leaves from outer scales, unfavorable accumulation of nutrients in bulbs, and easy necrosis of bulb tissues. To control the growth of callus, improve the efficiency of in vitro preservation, and save labor
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Embodiment 1
[0032] Embodiment 1: (in vitro preservation of oriental lily germplasm resources 1)
[0033] The specific method is as follows:
[0034] (1) The preparation of the culture medium: including the basic medium and the components of the medium for each stage of in vitro storage and the weight of each component in each liter of medium:
[0035] a) basic medium: wherein,
[0036] Induction medium is sucrose 40g / L, agar powder 4g / L, MS medium with pH5.8;
[0037] Proliferation medium is 50g / L sucrose, 5g / L agar powder, 3 / 5MS medium with pH5.6;
[0038] The medium for in vitro preservation and tube bulb expansion is 1 / 2MS medium with 60g / L sucrose, 5.0g / L agar powder, and pH5.6;
[0039] b) Induction medium I: MS+6-BA 1.0mg / L+IBA 0.1mg / L+AC 2.0mg / L;
[0040] c) Induction medium II: MS+6-BA 1.0mg / L+IBA 0.25mg / L;
[0041] d) Proliferation medium: 3 / 5MS+6-BA1.0mg / L+IBA0.5mg / L;
[0042] e) Synchronous culture medium for in vitro preservation and tube bulb expansion: 1 / 2MS+NAA 0.1mg / ...
Embodiment 2
[0050] Embodiment 2: (in vitro preservation of oriental lily germplasm resources 2)
[0051] In this example, the preparation of step (1) medium is:
[0052] a) basic medium: wherein,
[0053] Induction medium is 30g / L sucrose, 4.5g / L agar powder, MS medium with pH5.6;
[0054] Proliferation medium is 55g / L sucrose, 4.5g / L agar powder, 3 / 5MS medium with pH5.7;
[0055] The medium for in vitro preservation and tube bulb expansion is 1 / 2MS medium with 68g / L sucrose, 4.5g / L agar powder, and pH5.8;
[0056] b) Induction medium I: MS+6-BA 2.0mg / L+IBA 0.5mg / L+AC 1.0mg / L;
[0057] c) Induction medium II: MS+6-BA 0.75mg / L+IBA 0.1mg / L;
[0058] d) Proliferation medium: 3 / 5MS+6-BA0.2mg / L+IBA0.1mg / L;
[0059] e) Synchronous culture medium for in vitro preservation and tube bulb expansion: 1 / 2MS+NAA 0.5mg / L+PP333 5mg / L+mannitol 5.0g / L+AC 5.0mg / L;
[0060] Step (2) Provenance Bulb Treatment and Sterilization: Put 50 DEG C of incubator heat treatment 80min; Its sterilization treatment...
Embodiment 3
[0061] Embodiment 3: (in vitro preservation method 3 of oriental lily germplasm resources)
[0062] In this example, the preparation of step (1) medium is:
[0063] a) basic medium: wherein,
[0064] Induction medium is sucrose 50g / L, agar powder 5.0g / L, pH5.7 MS medium;
[0065] Proliferation medium is 3 / 5MS medium with sucrose 60g / L, agar powder 4.0g / L, pH5.8;
[0066] The medium for in vitro preservation and tube bulb expansion is 1 / 2MS medium with 75g / L sucrose, 4.0g / L agar powder, and pH6.0;
[0067] b) Induction medium I: MS+6-BA 1.5mg / L+IBA 0.3mg / L+AC 3.0mg / L;
[0068] c) Induction medium II: MS+6-BA 0.5mg / L+IBA 0.5mg / L;
[0069] d) Proliferation medium: 3 / 5MS+6-BA0.5mg / L+IBA0.3mg / L;
[0070] e) Synchronous culture medium for in vitro preservation and tube bulb expansion: 1 / 2MS+NAA 0.3mg / L+PP333 10mg / L+mannitol 3.0g / L+AC 3.0mg / L;
[0071] Step (2) Provenance Bulb Treatment and Sterilization: Heat treatment in 50°C incubator for 90 minutes; its sterilization treatm...
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