Culture medium for culturing orchid tissue and culture method thereof
A technology of tissue culture and culture medium, applied in horticultural methods, botany equipment and methods, angiosperms/flowering plants, etc., can solve the problems of inconsistent growth of seedlings, long time for slow seedlings, low seedling rate, etc. The effect of more leaves, faster seedling emergence, and increasing the percentage of large seedlings
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Embodiment 1
[0024] Embodiment one: prepare the culture medium of orchid tissue culture of the present invention
[0025] According to the formulation in Table 1 below, each component of 1 / 2 MS medium was weighed, wherein the amount of macroelements was half of that of standard MS medium.
[0026] Table 11 / 2 Composition and dosage of MS medium
[0027]
[0028]
[0029] 1. Preparation of Phalaenopsis tissue culture medium
[0030] According to the formula in Table 2 below, each component of the Phalaenopsis tissue culture medium was weighed.
[0031] Table 2 Phalaenopsis tissue culture medium composition and dosage
[0032] Sample serial number
White sugar
Medium No. 1
1 / 2MS medium
7g
15g
0.5g
100g
1g
Medium No. 2
1 / 2MS medium
8g
18g
1g
150g
2g
medium 3
1 / 2MS medium
9g
20g
1.5g
200g
2.5g
Med...
Embodiment 2
[0045] Embodiment two: Phalaenopsis tissue culture
[0046] 1. Adventitious bud induction: take robust and mature pedicels as explants, inoculate them in Phalaenopsis induction medium after disinfection (with 1 / 2MS as the basal medium, 5 mg of 6-benzylamino glands are added to each liter of 1 / 2MS medium purine, 0.5mg naphthaleneacetic acid and 100mL coconut water), after 25-35 days of culture, adventitious buds were induced from the pedicels;
[0047] 2. Inoculate adventitious buds in the Phalaenopsis proliferation medium (using MS as the basal medium, adding 8mg6-benzylaminoadenine, 0.5mg naphthaleneacetic acid and 100mL coconut water per liter of MS medium) for expansion culture, culture After 30 to 35 days, a large number of adventitious buds were obtained;
[0048] 3. With a sterilized scalpel, the adventitious buds are divided into small buds with 2 to 3 buds, and the small buds are inoculated in the Phalaenopsis tissue culture medium prepared in Example 1 to cultivate s...
Embodiment 3
[0056] Embodiment three: Cymbidium tissue culture
[0057] 1. Take healthy newborn axillary buds free from diseases and insect pests as explants, inoculate them in Cymbidium inoculation medium after disinfection (using MS as the base medium, adding 1.5mg of 6-benzylaminoadenine, 0.2 mg naphthalene acetic acid and 100g banana puree), after 25-30 days of cultivation, protocorms were induced;
[0058] 2. Inoculate the protocorm in the Cymbidium multiplication medium (based on MS, supplemented with 1.5mg of 6-benzylaminoadenine, 0.5mg of naphthaleneacetic acid and 100g of banana puree per liter of MS medium) for expansion Cultivate and obtain a large number of protocorms after 28 to 32 days of cultivation;
[0059] 3. Inoculate the protocorms in the Cymbidium phalanx tissue culture medium prepared in Example 1 for strong seedling cultivation, and after 28 to 35 days of cultivation, obtain Cymbidium cymbidium seedlings reaching the emergence standard.
[0060] The culture conditi...
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