Rapid propagation method for high quality seedlings of Kyara
A kind of technology of Agarwood and seedlings, which is applied in the field of rapid propagation of high-quality seedlings of Agarwood, can solve the problems of mother plant damage, the propagation of Agarwood tissue culture seedlings that have not yet been produced, and the difficulty of a large number of seeds, and achieves high application value , Simple and affordable technology
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Embodiment 1
[0017] Example 1: Tissue culture using young terminal buds of Aquilaria crassna Pierre ex Lecomte adult trees as explants
[0018] 1. Disinfection of explants and induction of adventitious buds: During the growing season, select the young terminal buds of the vigorous and excellent Chinese Agarwood adult tree as explants, soak them in 75% alcohol by volume for 10 seconds, and then use the mass fraction Disinfect with 0.1% mercuric chloride solution for 5 minutes, rinse with sterile water for 5 times, and then inoculate into adventitious bud induction medium for cultivation. Transfer to a new adventitious bud induction medium for the same culture, and then cultivate for about 30 days to form adventitious buds on the explants. The adventitious bud induction medium contains per liter: 6-benzylpurine 0.5mg, sucrose 20 grams, agar 6g, the remainder is the improved MS medium, pH5.8, and the described improved MS medium is to change the ammonium nitrate in the original MS medium int...
Embodiment 2
[0022] Example 2: Tissue culture using young stem nodes of Aquilaria crassna Pierre ex Lecomte adult trees as explants
[0023] 1. Disinfection of explants and induction of adventitious buds: During the growing season, select the young stem nodes of the vigorous and excellent Agarwood adult tree as explants, soak them in 75% alcohol by volume for 20 seconds, and then use the mass fraction Disinfect with 0.1% mercuric chloride solution for 8 minutes, wash with sterile water 4 times, inoculate into adventitious bud induction medium, culture temperature 26°C, light intensity 1800lx, light 14 hours / day, transfer to new adventitious bud induction culture after 25 days Adventitious buds can be formed on the explants after about 28 days of further culture. The adventitious bud induction medium per liter contains: 0.75 mg of 6-benzylpurine, 25 grams of sucrose, and 6 g of agar, and the balance is the improved MS culture base, pH5.9, the improved MS medium is to change the ammonium ni...
Embodiment 3
[0027] Example 3: Tissue culture using semi-lignified stem nodes of adult trees of Aquilaria crassna Pierre ex Lecomte as explants
[0028] 1. Disinfection of explants and induction of adventitious buds: During the growing season, select the semi-lignified stem nodes of the vigorous and excellent adult trees of Agarwood chinensis as explants, soak them in 75% alcohol for 30 seconds, and then use mass Sterilize with 0.1% mercuric chloride solution for 10 minutes, rinse with sterile water 5 times, inoculate into adventitious bud induction medium, cultivate at 28°C, illuminance 2000lx, light 16 hours / day, and transfer to new adventitious bud induction after 25 days Culture medium, after culturing for about 25 days, adventitious buds can be formed on the explants. The adventitious bud induction medium contains per liter: 1 mg of 6-benzylpurine, 30 grams of sucrose, 6 g of agar, and the balance is an improved MS medium, pH 6.0. The improved MS medium is the original The ammonium ...
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