A kind of high borneol content borneol camphor tissue culture breeding method
A technology of borneol camphor content and borneol camphor content is applied in the field of borneol camphor camphor tissue culture and breeding with high borneol content, and can solve the problems such as the lack of clear explant material borneol content and the like.
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Embodiment 1
[0026] a, the establishment of sterile line: with the high-content borneol camphor tree of 90%~97% borneol content in the leaf essential oil, the year-old branches are used as explants, the leaves and terminal buds are cut off, and the lower part of the terminal buds contains 4~5 For the stem section of an axillary bud, clean the surface with detergent, soak it in alcohol for 30 seconds on the ultra-clean workbench, and then sterilize it with 5% sodium hypochlorite solution for 6 minutes, then sterilize it with 0.1% mercuric chloride for 5-6 minutes, and then sterilize it with Rinse 5-6 times with sterile water, cut off about 0.5 cm at both ends of the stem segment, and cut the stem segment into small segments with 1-2 axillary buds depending on the length of the internodes, inoculate them in the induction medium, and grow them under light intensity of 2000-2000 3000Lux, 12h / day, culture at 20-30℃. After about 1 week of cultivation, the axillary buds on the stems begin to expan...
Embodiment 2
[0032] a, the establishment of sterile line: with the high-content borneol camphor tree of 90%~97% borneol content in the leaf essential oil, the year-old branches are used as explants, the leaves and terminal buds are cut off, and the lower part of the terminal buds contains 4~5 For the stem section of an axillary bud, clean the surface with detergent, soak it in alcohol for 30 seconds on the ultra-clean workbench, and then sterilize it with 5% sodium hypochlorite solution for 6 minutes, then sterilize it with 0.1% mercuric chloride for 5-6 minutes, and then sterilize it with Rinse 5-6 times with sterile water, cut off about 0.5 cm at both ends of the stem segment, and cut the stem segment into small segments with 1-2 axillary buds depending on the length of the internodes, inoculate them in the induction medium, and grow them under light intensity of 2000-2000 3000Lux, 12h / day, culture at 20-30℃. After about 1 week of cultivation, the axillary buds on the stems begin to expan...
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