Tissue-culture rapid propagation method for arundina graminifolia
A technology for tissue culture and rapid propagation and bamboo leaf orchid, which is applied in the field of plant tissue culture, can solve the problems such as inability to obtain genetic material seedlings, easy separation of traits, etc., and achieves easy establishment of sterile lines, shortening induction time, and improving production efficiency. and profit effects
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Embodiment 1
[0020] The method for rapid propagation of bamboo leaf orchid tissue culture of the present invention comprises the following steps:
[0021] Step 1 Explant material selection and surface disinfection:
[0022] Take high-position buds that are more than 10 cm away from the upper surface of the cultivation medium and full of high-position buds with a length of 3-5 cm as the selection material, cut off the high-position buds as explants, first rinse them under tap water, and then under sterile conditions, use 70 Disinfect with -75% alcohol for 30-60 seconds, rinse once with sterile water, then disinfect with 0.1% mercury liter for 8-12 minutes, rinse with sterile water for 3-5 times, and blot dry with sterile filter paper for later use.
[0023] Induction culture of step 2 adventitious buds:
[0024] Under sterile conditions, first cut off the top 1-3 cm of the sterilized high buds, and then inoculate the remaining part with the plant growth regulator 6-BA3.0mg / L+NAA0.1mg / L wit...
Embodiment 2
[0032] Step 1 Explant material selection and surface disinfection:
[0033] Take high-position buds that are more than 10 cm away from the upper surface of the cultivation medium and full of high-position buds with a length of 3-5 cm as the selection material, cut off the high-position buds as explants, first rinse them under tap water, and then under sterile conditions, use 70 Disinfect with -75% alcohol for 30-60 seconds, rinse once with sterile water, then disinfect with 0.1% mercury liter for 8-12 minutes, rinse with sterile water for 3-5 times, and blot dry with sterile filter paper for later use.
[0034] Induction culture of step 2 adventitious buds:
[0035] Under sterile conditions, first cut off the top 1-3 cm of the sterilized high buds, and then inoculate the remaining part with the plant growth regulator TDZ0. On the MS medium, culture in the cultivation room under light, keep the light intensity 1500-2000LX, the light time is 12 hours a day, the temperature is 2...
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