Quick seedling cultivating method for red honeysuckle stems
A technology of honeysuckle and stem segments, which is applied in the field of rapid seedling growth of red honeysuckle stem segments, which can solve the problems of plant carrying, poor growth and development, and low plant survival rate, and achieve good growth, fast survival, and high survival rate.
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Embodiment 1
[0021] A kind of rapid seedling-forming method of red honeysuckle stem section, comprises the following steps:
[0022] S1, collect 2-year-old young shoots of red honeysuckle with internodes, remove leaves, soak in 2% washing powder solution for 10 minutes to remove surface dirt, then rinse with tap water for 1 hour and soak for 30 minutes, then rinse repeatedly with sterile water for 3- 5 times, in a sterile environment, soak in ethanol with a volume concentration of 75% for 15 seconds, then rinse with sterile water, then put it into a mercuric chloride solution with a mass concentration of 0.2%, stir for 3 minutes, take it out and rinse with sterile water 5-6 times, and finally use sterile filter paper to absorb the moisture on the surface of the branches to obtain sterile branches;
[0023] S2, add sucrose and agar to MS medium, and obtain basal medium after high temperature and high pressure sterilization; add 6-BA (6-benzylaminopurine), NAA (naphthaleneacetic acid), KT (k...
Embodiment 2
[0027] A kind of rapid seedling-forming method of red honeysuckle stem section, comprises the following steps:
[0028] S1, collect 2-year-old young shoots of red honeysuckle with internodes, remove leaves, soak in 2% washing powder solution for 13 minutes to remove surface dirt, then rinse with tap water for 1 hour and soak for 35 minutes, then rinse repeatedly with sterile water for 3- 5 times, soak in ethanol with a volume concentration of 75% for 20s in a sterile environment, then rinse with sterile water, then put it into a mercuric chloride solution with a mass concentration of 0.2%, stir for 3 minutes, take it out and rinse with sterile water 5-6 times, and finally use sterile filter paper to absorb the moisture on the surface of the branches to obtain sterile branches;
[0029] S2, add sucrose and agar to MS medium, and obtain basal medium after high temperature and high pressure sterilization; add 6-BA (6-benzylaminopurine), NAA (naphthaleneacetic acid), KT (kinetin ...
Embodiment 3
[0033] Discussion on the optimal addition amount of different hormones (6-BA, NAA, KT) in the induction medium:
[0034] Test material: the aseptic branch of band axillary bud in the S1 of embodiment 1 is cut into 1cm stem section;
[0035] Test method: the final concentration of 6-BA is 1.0mg / L, 1.5mg / L, the final concentration of NAA is 0.1mg / L, 0.2mg / L, and the final concentration of KT is 0.5mg / L, 1.0mg / L, 1.5 mg / L, 12 kinds of induction medium were made by orthogonal combination. Inoculate test materials in 12 kinds of induction media respectively, calculate germination rate and contamination rate, wherein contamination rate=contamination number / inoculation number×100%, germination rate=germination number / (total number of buds-pollution bud number)×100% , the induction medium preparation method and the culture method are all consistent with Example 1. The results are shown in Table 1:
[0036]Table 1 Effects of induction media with different concentrations and ratios on...
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