Jojoba tissue cultivation quick breeding method
A rapid and basic medium technology, applied in the field of artificial propagation and cultivation of plants, can solve the problems of serious glass seedlings, long rooting time, low multi-bud rate, etc., to save land for seedlings, reduce production costs, and stabilize genetic traits Effect
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Embodiment 1
[0015] 1. Take the stem tip of the jojoba plant material, wash it with running water for 8-12 hours, absorb excess water with filter paper, then disinfect it with 0.1% mercury dichloride for 3-5 minutes, and rinse it with sterile water until clear.
[0016] 2. Trim the material washed to clear to more than 0.3 cm, and inoculate it into the starting medium of the present invention. The composition ratio of the starting medium is: 200 mg / liter of hydrolyzed milk protein is added to the 4736.43 mg / liter MS basic medium , 6-furfuryl purine 2 mg / L, 6-benzyl purine 0.5 mg / L, edible sugar 25 g / L, and the balance of water. Place the inoculation chamber for light cultivation.
[0017] 3. Cut the test-tube plantlets cultivated more than 3 centimeters into stems of more than 0.5 centimeters respectively, and inoculate them into the proliferation medium of the present invention. The composition ratio of the proliferation medium includes adding inositol in 4736.43 mg / liter MS basic medium ...
Embodiment 2
[0021] 1. Take the stem section of the jojoba plant material, rinse it with running water for 12-24 hours, absorb excess water with filter paper, then routinely disinfect it with 0.1% mercury dichloride, and rinse it with sterile water until clear.
[0022] 2. Trim the material washed to clear to more than 0.3 centimeters. Inoculate into the starting medium of the present invention, the composition ratio of starting medium is: add hydrolyzed milk protein 200 mg / liter in 4736.43 mg / liter MS basic medium , 1 mg / L of 6-furfuryl purine, 0.5 mg / L of 6-benzyl purine, 25 g / L of edible sugar, and the remainder of water were placed in the inoculation room for light cultivation.
[0023] 3. Cut the test-tube plantlets cultivated more than 3 centimeters into stem sections more than 0.5 centimeters respectively. Inoculate in the proliferation medium of the present invention, the composition ratio of the proliferation medium is: add muscle in 4736.43 mg / liter MS basic medium Alcohol 500 mg...
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