Tissue culture method for fast propagation of primula denticulata ssp.sino-denticulata
A technology of tissue culture rapid propagation and ball flowering, which is applied in the field of plant tissue culture, can solve the problems that the method of division propagation cannot meet the production needs, and there is no relevant research and report on tissue culture, so as to shorten the seedling cycle and have strong consistency , the effect of easy seedling growth
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Embodiment 1
[0024] Using the leaves of Primula denticulata ssp.sino-denticulata as explants to explore the optimal medium for adventitious bud induction: the leaves of well-growing seedlings were used as explants to explore the optimal medium formula for adventitious bud induction. Take the young leaves of Primuladenticulata ssp.sino-denticulata and wash them with tap water for 5-6 hours, drop a drop of detergent in the water and shake for 15 minutes, gently brush off surface impurities with a soft brush, and rinse them with tap water repeatedly; Surface disinfection: disinfect with 70% alcohol for 15-20 seconds, rinse with sterile water for 4-5 times, disinfect with 0.1% mercury chloride solution for 4-5 minutes, and rinse with sterile water for 4-5 times. The sterilized leaves were then cut into 1 cm 2 Small pieces (with part of the veins) were inoculated on the induction medium of clustered buds, 5-6 pieces were inoculated in each bottle, and 10 bottles were connected to each medium, a...
Embodiment 2
[0027] The axillary buds of Primula denticulata ssp.sino-denticulata in northern Yunnan were used as explants for primary culture and subculture: select axillary buds from robust plants, rinse them with tap water for 5-6 hours, and disinfect the same process as the leaves , inoculated on MS+6-BA 2.0mg / l+NAA0.1mg / l cluster bud induction medium, inoculated 2 to 3 buds per bottle; the light conditions were natural scattered light 3000Lux plus artificial auxiliary light source 1800±200Lux, light Time 14h.
[0028] When the axillary buds are inoculated on the differentiation medium, new leaves are continuously pulled out. From 10 days on, the petioles of the new leaves are thick and the base turns red, and light green callus is gradually formed. After 2 weeks, adventitious buds begin to differentiate; 40 days after inoculation , A large number of adventitious buds are differentiated on the newly drawn petioles and leaves of the axillary buds.
[0029]Statistical results show that ...
Embodiment 3
[0031] Rooting culture of Primula denticulata ssp.sino-denticulata tissue culture seedlings: when the adventitious buds grew 2-3 leaves on the differentiation medium, they were excised from the callus and transferred to Rooting medium, formula: MS, MS+NAA (0.1mg / l, 0.2mg / l, 0.5mg / l), pH 5.8; light conditions: natural scattered light 3000Lux plus artificial auxiliary light source 2500Lux, light time 14h .
[0032] From the perspective of the time required for rooting, the time required for rooting in medium MS and MS+0.2mg / l NAA is the shortest, 8-10 days, but in MS+0.2mg / l NAA, the rooting amount of tissue culture seedlings And growth is obviously better than MS basic medium, the average height of tissue culture seedlings can reach 4.8cm, and the rooting rate is over 95%.
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