Method for promoting tissue culture seedling of anisetree bark to take root rapidly
A technology of tissue cultured seedlings and maple bark, which is applied in the field of plant asexual reproduction, can solve the problems of low survival rate of tissue cultured seedlings transplanted, hindering the application of rapid propagation technology of tissue cultured seedlings, and difficulty in rooting tissue cultured seedlings, etc. The effect of planting survival rate, protecting the diversity of ecological environment and shortening the rooting time
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Embodiment 1
[0017] A method for promoting rapid rooting of maple bark tissue culture seedlings, comprising the following steps:
[0018] (1) On the ultra-clean workbench, multiply and cultivate the maple bark to obtain aseptic buds with a height of 2 to 3 cm, cut them into single buds, and soak the base in a sterilized rooting agent for 60 min; the rooting agent is : NAA 100 mg / L+IAA 500 mg / L+CPPU 0.001 mg / L +Vc 5.0 mg / L, pH 5.5;
[0019] (2) Take out the single bud of step (1) and put it in a sterile tray for 30 minutes, inoculate it in solid medium 1 / 2MS+ Activated carbon 1g / L + sucrose 20 g / L + agar 5 g / L, pH value 7.0, after 10 days of culture, the stem segment 1 cm above the base slightly swelled, and adventitious roots began to grow from the swollen stem segment and base at 25 days, and at 45 days The growth of adventitious roots is relatively stable, and the number of roots reaches the maximum. The number of roots per plant is about 18.2, and the rooting rate is 100%. The roots ar...
Embodiment 2
[0022] A method for promoting rapid rooting of maple bark tissue culture seedlings, comprising the following steps:
[0023] (1) On the ultra-clean workbench, multiply and cultivate the maple bark to obtain aseptic buds with a height of 2 to 3 cm, cut them into single buds, and soak the base in a sterilized rooting agent for 30 min; the rooting agent is : NAA 800 mg / L+IAA 2000 mg / L+CPPU 0.01mg / L +Vc 2.0mg / L, pH value is 5.5;
[0024] (2) Take out the single bud of step (1) and put it in a sterile tray for 15 minutes, inoculate it in solid medium 1 / 2MS+activated carbon 1g / L+sucrose 20g / L+agar 5g / L, pH value is 7.0, and culture for 5 After 1 day, the stem section 1 cm above the base was slightly enlarged, and adventitious roots began to grow from the enlarged stem section and base at 18 days, and the growth of adventitious roots was relatively stable at 50 days, and the number of roots reached the maximum, and the number of roots per plant was about 23.5 The rooting rate is 100...
Embodiment 3
[0027] A method for promoting rapid rooting of maple bark tissue culture seedlings, comprising the following steps:
[0028] (1) On the ultra-clean workbench, multiply and cultivate the maple bark to obtain aseptic buds with a height of 2 to 3 cm, cut them into single buds, and soak the base in a sterilized rooting agent for 45 min; the rooting agent is : NAA500 mg / L+IAA1500 mg / L+CPPU0.004 mg / L +Vc8.0 mg / L, pH value is 5.5;
[0029] (2) Take out the single bud from step (1) and put it in a sterile tray for 20 minutes, inoculate it in solid medium 1 / 2MS + activated carbon 1g / L + sucrose 20g / L + agar 5g / L, pH value 7.0, culture for 5d Afterwards, the stem segment 1 cm upward from the base was slightly enlarged, and adventitious roots began to grow from the enlarged stem segment and base at 20 days, and the growth of adventitious roots was relatively stable at 45 days, and the number of roots reached the maximum. The number of roots per plant was about 31.3, and the rooting rate ...
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