Method for inducing castanea henryi tissue culture seedling leaves to generate adventitious roots
A technology of tissue culture seedlings and leaves, applied in the field of plant tissue culture, can solve the problems of low multiplication coefficient, easy browning, difficult rooting, etc.
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Embodiment 1
[0038] A method for inducing the direct generation of adventitious roots from leaves of tissue-cultured plantlets of Chestnut, comprising the following steps:
[0039]S1. Cultivation of Chinese chestnut tissue culture seedlings: Peel the seeds of Chinese chestnut, wash them with tap water for 20 minutes, disinfect them with 75% alcohol for 90 seconds on the ultra-clean workbench, rinse them with sterile water for 3 times; then wash them with 0.1% alcohol mercuric chloride solution for 9 minutes, rinse with sterile water 5 to 6 times. On the filter paper after high-temperature sterilization, part of the cotyledons of the seeds were excised with a sterile blade to obtain seed embryos with a size of 1 cm×0.6 cm×0.6 cm. Inoculate into the first MS medium after autoclaving. Placed in a light culture room for 25-35 days. The temperature of the light cultivation room is 27±1°C; the light cycle is 14 / 10h, and the light intensity is 50molm -2 the s -1 . The above mediums all conta...
Embodiment 2
[0051] A method for inducing the direct generation of adventitious roots from leaves of tissue-cultured plantlets of Chestnut, comprising the following steps:
[0052] S1. Cultivation of Chinese chestnut tissue culture seedlings: Peel the seeds of Chinese chestnut, wash them with tap water for 20 minutes, disinfect them with 75% alcohol for 90 seconds on the ultra-clean workbench, rinse them with sterile water for 3 times; then wash them with 0.1% alcohol mercuric chloride solution for 9 minutes, rinse with sterile water 5 to 6 times. On the filter paper after high-temperature sterilization, part of the cotyledons of the seeds were excised with a sterile blade to obtain seed embryos with a size of 1 cm×0.6 cm×0.6 cm. Inoculate into the first MS medium after autoclaving. Placed in a light culture room for 25-35 days. The temperature of the light cultivation room is 27±1°C; the light cycle is 14 / 10h, and the light intensity is 50molm -2 the s -1 . The above mediums all cont...
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