A method for inducing plant regeneration from embryoid bodies of head cabbage
A technology for regenerating plants and cabbage, applied in the field of plant tissue culture, can solve the problems of low induction rate and low induction rate of microspores, and achieve the effects of high value-added coefficient and high genetic stability
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Embodiment 1
[0017] 1. Induction of sterile seedlings: select firm and plump cabbage seeds, clean the seeds with tap water, disinfect them in 70-75% ethanol for 15 seconds, and disinfect them in a sodium hypochlorite solution with a volume concentration of 3% for 10 minutes. Wash the seeds with tap water after autoclaving and cooling; inoculate the sterilized seeds in the sterile seedling induction medium, and cultivate them in a sterile culture room: the culture conditions are temperature 18-22°C, light 1500-2000Lx, air humidity 50%-60%, when the sterile seedlings are cultivated to 5-8cm, take the sterile seedlings out of the cultivation room, and clean them with cooled high-pressure sterilized water;
[0018] 2. Induction of embryoid bodies: In an aseptic operating table, select the hypocotyls of the sterile cabbage seedlings as explants, cut the hypocotyls into 3-4mm segments, and inoculate them in the embryoid body induction medium 5 explants were inoculated in each bottle of medium, a...
Embodiment 2
[0025] The induction process is the same as in Example 1, except that the embryoid body induction medium formula is: add 1mg / L indoleacetic acid, 0.1mg / L 6-glycosylaminopurine, 30g / L sucrose in every 1L MS medium , 7g / L agar; the medium formula for regenerated plants is: add 1mg / L naphthaleneacetic acid, 0.5mg / L 6-glycosylaminopurine, 30g / L sucrose, and 7g / L agar to each 1L MS medium. The induction rate of embryoid bodies was 85%, and the induction rate of regenerated plants was 88%.
Embodiment 3
[0027] The induction process is the same as in Example 1, except that the embryoid body induction medium formula is: add 1.5mg / L indoleacetic acid, 1mg / L 6-glycosylaminopurine, 30g / L sucrose in every 1L MS medium , 7g / L agar; the medium formula for regenerated plants is: add 1.5mg / L naphthaleneacetic acid, 1mg / L 6-glycosylaminopurine, 30g / L sucrose, and 7g / L agar to each 1L MS medium. The induction rate of embryoid bodies was 80%, and that of regenerated plants was 75%.
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