Method for tissue culture of Japanese premna
A technology of Vitex stinky tissue and culture method, applied in the field of culture of Vitex stinky tissue, to achieve the effect of increasing the number of plants and shortening the culture time
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Embodiment 1
[0029] The test material is 2 young 21cm branches of Vitex stinky less than one year old
[0030] (1) Preparation of explants: take the branches of Vitex stinkii for less than one year, and cut them into 3 cm long stem segments with scissors, ensuring that each stem segment has 1 leaf bud.
[0031] (2) Aseptic operation: the stem joints are washed with water, placed in 70% alcohol for 25 seconds, taken out and placed in 10% sodium hypochlorite solution for 15 minutes, washed twice with sterile water.
[0032] (3) Germination culture: sterilized stem segments were inoculated into 1 liter of MS medium plus 0.1 mg of 6-BA, pH 5.8, and germinated on the germination medium at 23° C. for 4 days.
[0033] (4) Rooting culture: the rooting medium was 1 liter of MS medium plus 0.3 mg of IBA and 0.4 mg of NAA, pH 5.8, and rooting was induced on the rooting medium at 23° C. for 10 days.
[0034] (5) After the root system grows and matures, it is transplanted into organic matter soil, cov...
Embodiment 2
[0037] The test material is 2 mature branches of the annual stinky Vitex 20cm branch
[0038] (1) Preparation of explants: Take annual Vitex stifolium branches, cut them into 5 cm long stem segments with scissors, and ensure that each stem segment has 3 leaf buds.
[0039] (2) Aseptic operation: the stem joints are washed with water, placed in 70% alcohol for 35 seconds, taken out and placed in 10% sodium hypochlorite solution for 25 minutes, and washed 4 times with sterile water.
[0040] (3) Germination culture: sterilized stem segments were inoculated into 1 liter of MS medium plus 0.1 mg of 6-BA, pH 6.0, and germinated on the germination medium at 25° C. for 6 days.
[0041] (4) Rooting culture: the rooting medium was 1 liter of MS medium plus 0.5 mg of IBA and 0.6 mg of NAA, pH 6.0, and induced rooting at 25° C. for 20 days on the rooting medium.
[0042] (5) After the root system grows and matures, transplant it into organic matter soil, cover with plastic cloth, and cu...
Embodiment 3
[0045] The test material is two semi-lignified branches of biennial stinky Vitex 20cm branches
[0046] (1) Preparation of explants: take biennial Vitex stifolium branches, cut them into 4 cm long stem segments with scissors, and ensure that each stem segment has 2 leaf buds.
[0047] (2) Aseptic operation: the stem joints are washed with water, placed in 70% alcohol for 30 seconds, taken out and placed in 10% sodium hypochlorite solution for 20 minutes, and washed 3 times with sterile water.
[0048] (3) Germination culture: the sterilized stem segments were inoculated into 1 liter of MS medium plus 0.5 mg of 6-BA, pH 5.9, and germinated on the germination medium at 24° C. for 5 days.
[0049] (4) Rooting culture: the rooting medium was 1 liter of MS medium plus 0.4 mg of IBA and 0.5 mg of NAA, pH 5.9, and rooting was induced for 15 days at 24° C. on the rooting medium.
[0050] (5) After the root system grows and matures, transplant it into organic matter soil, cover with p...
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