Method for efficiently and rapidly propagating Dendrobium candidum test-tube seedlings in large scale
A technology of Dendrobium officinale and test-tube seedlings is applied in the field of plant cultivation, which can solve the problems of vitrification and large variation rate of seedlings, low transplanting survival rate, low seed germination rate, etc., and achieves shortened germination time and transplanting adaptability. Good, the effect of increasing growth rate
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Embodiment 1
[0027] (1) On the ultra-clean workbench in the inoculation room, place the uncracked Dendrobium candidum capsules in a jar, pour 70% (v / v) alcohol into the bottle, soak for about 50s, and filter out the alcohol. Then soak in 0.1% (w / w) mercuric chloride aqueous solution for about 12 to 15 minutes, repeatedly shake horizontally during the soaking process, so that the surface of the capsules can be thoroughly disinfected, and then rinse repeatedly with sterile water for 3 to 4 times, and the sterilized capsules Cut open and take the seeds for later use.
[0028] (2) Dendrobium officinale seeds are sown in the liquid medium of 1 / 4MS medium+6-benzylpurine 0.2mg / L+naphthaleneacetic acid 0.2mg / L+potato juice 80g / L+sucrose 25g / L, pH 5.4; Put it into a constant temperature shaking incubator for shaking culture. The culture conditions of the shaking incubator are set at a temperature of 25°C, a rotation speed of 120-150r / min, an illumination of 300-1000 lux, and a light time of 12h / d. ...
Embodiment 2
[0033] Except that in step (2) of the embodiment 1, the seed is sown in the liquid medium and the vibration culture is changed to the solid medium for germination, and the step (5) the natural light and sunlight cultivation in the greenhouse is changed to the fluorescent lamp cultivation in the cultivation room, the others are the same as the embodiment 1; steps (2), step (3), step (4) in seed germination, strong seedling cultivation, strong seedling rooting cultivation three stages are screened respectively with the substratum combination listed in Table 1, to optimize the optimum substratum combination formula. Table 1 illustrates: ① The optimization of the medium formula is mainly to design different basic medium, hormone concentration, natural additives, activated carbon concentration, etc. to optimize the design of the medium. In this example, it is designed as a solid medium. The agar concentration was 5g / L, the sucrose was 25g / L, and the culture environment was a culture...
Embodiment 3
[0039] Others are the same as in Example 1, the Dendrobium officinale seeds obtained in step (1) are sown respectively in the following 4 different mediums: 1. 1 / 4MS medium+6-benzylpurine 0.2mg / L+naphthaleneacetic acid 0.2mg / L+potato Juice 80g / L+sucrose 25g / L+pH 5.4 liquid medium; ②1 / 4MS medium+6-benzylpurine 0.2mg / L+naphthaleneacetic acid 0.2mg / L+banana juice 100g / L+sucrose 25g / L+pH 5.4 liquid culture ③ MS medium + 6-benzylpurine 0.2mg / L + naphthaleneacetic acid 0.2mg / L + potato juice 80g / L + sucrose 25g / L + pH 5.4 liquid medium; ④ 1 / 4 MS medium + 6-benzylpurine 0.2mg / L+naphthaleneacetic acid 0.2mg / L+potato juice 80g / L+sucrose 25g / L+agar 5.0g / L+pH 5.4 solid medium. The culture environment of the liquid medium was set at a temperature of 25°C, a rotational speed of 120r / min, an illuminance of 1000 lux, and a light time of 12h / d, and the culture was shaken. The culture environment of the solid medium was set at a temperature of 25°C, an illuminance of 1000 lux, and a light tim...
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