Thymus mongolicus Ronn. tissue culture rapid propagation method
A technology of incense group and culture temperature, applied in the field of plant tissue culture, can solve the problems of wild resources depletion, wild resources can not meet the needs, yield and quality decline, etc., and achieve the effect of improving reproductive efficiency, speeding up breeding and promotion
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Embodiment 1
[0018] (1) Induction culture: cut the sterilized stem segments into about 0.5 cm, and inoculate them into the induction medium in a flat inoculation method. After inoculation, culture it in the dark, and after the callus appears, move it to the light for 12 hours a day, the light intensity is 1000lx, the culture temperature is 25°C, and the relative air humidity is 75% after 30 days of culture. The induction rate Reached 96.2%. The induction medium is: MS+1.5mg / L KT+0.8mg / L NAA+25g / L sucrose+3.5g / L agar, with a pH of 5.4.
[0019] (2) Proliferation culture: the callus induced by step (1) is transferred to the proliferation medium for propagation. After inoculation, place under the conditions of 12 hours of light per day, light intensity of 2000lx, culture temperature of 25°C, and relative air humidity of 75% for 30 days, and the proliferation coefficient reaches 4.8. The proliferation medium is: MS+0.6mg / L 6-BA+1.5mg / LNAA+25g / L sucrose+3.5g / L agar, with a pH of 5.4.
[0020...
Embodiment 2
[0024] (1) Induction culture: cut the sterilized stem segments into about 0.5 cm, and inoculate them into the induction medium in a flat inoculation method. After inoculation, culture in dark conditions, and then move to place in the light for 14 hours a day when the callus appears, the light intensity is 2000lx, the culture temperature is 27°C, and the relative air humidity is 75% after 30 days of culture and the induction rate Reached 92.8%. The induction medium is: MS+3.5mg / L KT+1.0mg / L NAA+30g / L sucrose+3.5g / L agar, with a pH of 5.4.
[0025] (2) Proliferation culture: the callus induced by step (1) is transferred to the proliferation medium for propagation. After inoculation, place under the conditions of 14 hours of light per day, light intensity of 2000lx, culture temperature of 27°C, and relative air humidity of 75% for 30 days, and the proliferation coefficient reaches 5.1. The proliferation medium is: MS+1.0mg / L 6-BA+2.0mg / LNAA+25g / L sucrose+3.5g / L agar, wi...
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