A method of culturing osmunda japonica tissues
A technology of tissue culture and Osmanthus japonica, applied in horticultural methods, botanical equipment and methods, plant cells, etc., can solve problems such as seasonal cutting restrictions, and achieve the effect of breaking through seasonal restrictions
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Embodiment 1
[0048] The steps of the tissue culture of Osmanthus fruticosa are as follows:
[0049] 1. Remove all the expanded leaves and roots of the Osmanthus cabbage, leaving only the young stem tip, and rinse it with tap water. Then disinfect it with 0.1% mercury liter for 5-20 minutes on the ultra-clean workbench, and finally rinse it with sterile water for later use.
[0050] 2. Insert the sterilized stem tips of Osmanthus chinensis into the induction medium, culture in the dark at 20°C-27°C for 3-7 days, and then light culture, the intensity gradually increases from weak to strong. A large number of protocorms can be formed on young leaves in about 20-40 days.
[0051] Based on the dosage of one liter of medium, the formulation of induction medium is:
[0052] MS 250ml
[0053] Kinetin 0.5 mg
[0054] Sodium dihydrogen phosphate 100 mg
[0055] Activated Charcoal 1000mg
[0056] Sucrose 30000 mg
[0057] Agar 9000 mg
[0058] 3. Protocorms continue to be cultivated for 30 da...
Embodiment 2
[0076] The steps and culture conditions of Weicai tissue culture are the same as in Example 1, and the induction medium formula is (with the consumption of one liter of medium)
[0077] MS 2500ml
[0078] Kinetin 2mg
[0079] 3-Indolebutyric acid 2mg
[0080] Sodium dihydrogen phosphate 1000mg
[0081] Activated Charcoal 2000mg
[0082] Sucrose 30000mg
[0083] Agar 9000mg
[0084] The subculture medium formula is (according to the amount of one liter of medium)
[0085] MS 2500ml
[0086] Kinetin 2mg
[0087] 3-Indolebutyric acid 2mg
[0088] Sodium dihydrogen phosphate 1000mg
[0089] Activated Charcoal 2000mg
[0090] Sucrose 30000mg
[0091] Agar 9000mg
[0092] The formula of rooting medium is (in the amount of one liter of medium)
[0093] MS 2500ml
[0094] Kinetin 2mg
[0095] Sodium dihydrogen phosphate 1000mg
[0096] Activated Charcoal 2000mg
[0097] Sucrose 30000mg
[0098] Agar 9000mg
Embodiment 3
[0100] The steps and culture conditions of Weicai tissue culture are the same as in Example 1, and the induction medium formula is (with the consumption of one liter of medium)
[0101] MS 4000ml
[0102] Kinetin 4 mg
[0103] 3-indolebutyric acid 4 mg
[0104] Sodium dihydrogen phosphate 2000mg
[0105] Activated Charcoal 3000 mg
[0106] Sucrose 30000mg
[0107] Agar 9000mg
[0108] The subculture medium formula is (according to the amount of one liter of medium)
[0109] MS 4000ml
[0110] Kinetin 4 mg
[0111] 3-indolebutyric acid 4mg
[0112] Sodium dihydrogen phosphate 2000mg
[0113] Activated Charcoal 3000 mg
[0114] Sucrose 30000 mg
[0115] Agar 9000mg
[0116] The formula of rooting medium is (in the amount of one liter of medium)
[0117] MS 4000ml
[0118] Kinetin 4 mg
[0119] Sodium dihydrogen phosphate 2000 mg
[0120] Activated Charcoal 3000 mg
[0121] Sucrose 30000 mg
[0122] Agar 9000mg
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