Tissue culture method of vaccinium dunalianum containing caffeoyl arbutin
A technique for caffeoyl arbutin and tissue culture, which is applied in the field of plant tissue culture, can solve problems such as lack of resources of camphor bilberry, and achieves the effects of good application prospect, low price and simple culture process.
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Embodiment 1
[0030] (1) Initiation culture of axillary bud induction
[0031] Obtain the young and tender vaccinia vaccinia stems of the year as explants from robust vaccinia plants, cut off the leaves of the explants and cut them into 4-6 cm long stems, soak them in detergent water for 30-60 minutes , rinse with running water for 1 to 2 hours, then disinfect with 75% alcohol and 0.1% mercuric chloride, soak in 75% alcohol for 15 to 30 seconds, soak in 0.1% mercuric chloride for 7 to 12 minutes, and rinse with sterile water for 4 to 10 minutes after disinfection. 5 times, cut it into a stem section with 1-2 leaf axils on sterilized filter paper and blot the water on the stem section, then insert the leaf axil upwards obliquely in the axillary bud induction medium (WPM+6-BA2.5mg / L+NAA1.0mg / L+activated carbon 2.5g / L, in which white sugar 20~30g / L, agar 4-6g / L, pH5.5), the culture temperature is 25±2℃, the light intensity is 2000lx, light The cycle ratio is 14h:10h. After 25 days of cultur...
Embodiment 2
[0039] (1) Initiation culture of axillary bud induction
[0040] Obtain the young and tender vaccinia vaccinia stems of the year as explants from robust vaccinia plants, cut off the leaves of the explants and cut them into 4-6 cm long stems, soak them in detergent water for 30-60 minutes , rinse with running water for 1 to 2 hours, then disinfect with 75% alcohol and 0.1% mercuric chloride, soak in 75% alcohol for 15 to 30 seconds, soak in 0.1% mercuric chloride for 7 to 12 minutes, and rinse with sterile water for 4 to 10 minutes after disinfection. 5 times, cut it into a stem section with 1-2 leaf axils on sterilized filter paper and blot the water on the stem section, then insert the leaf axil upwards obliquely in the axillary bud induction medium (WPM+6-BA2mg / L +NAA1.5mg / L+activated carbon 3g / L, in which white sugar 20~30g / L, agar 4~6g / L, pH5.4), culture on 27±2℃, light intensity 2500lx, light cycle ratio 15h :9h. After 30 days of cultivation, the bud induction rate was ...
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