High-seedling-rate culture method for tissue culture of Polygala fallax stems
A cultivation method and technology of seedling success rate, applied in the field of propagation of Polygala chrysogenum seedlings, can solve problems such as rapid propagation and popularization of unfavorable good varieties, no test-tube seedling transplanting management, and easy variation of offspring seedlings, etc., to achieve rapid Effects of reproduction, prevention of vitrification and callus, and avoidance of basal callus
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[0047] The method for cultivating high seedling rate through tissue culture of Polygala chrysanthemum stem section comprises the following steps:
[0048] (1) Collection and disinfection of explants: collection of semi-lignified branches with ungerminated axillary buds of Polygala chrysanthemum, removing leaves, cutting at least one internode stem segment as explants, and disinfecting it;
[0049] (2) Obtain axillary buds by inducing culture: cut off the two ends of the above-mentioned sterilized explants in contact with the disinfectant, leave a stem section with at least one internode, and then obliquely cut the morphological lower end of the stem section Insert on the axillary bud induction medium that induces axillary bud germination to carry out axillary bud induction culture for 15-20 days,
[0050] Axillary bud induction culture conditions are: temperature 20±2°C, dark conditions without light;
[0051] Through the above treatment, invisible axillary buds germinate and...
example 1
[0076](1) Collection and disinfection of explants: On sunny days for 5 consecutive days, without watering the day before, cut the semi-lignified branches of the chrysanthemum chrysalis with ungerminated axillary buds, remove the leaves, and cut the segmented stems as explants. For the plant, use alcohol cotton balls with a mass concentration of 75% to wipe the stem explants for 2 times, then place them on the ultra-clean workbench, cut them into stems with 1 internode, and use 0.1% carbon dioxide Soak in chlorine for 12 minutes, rinse with sterile water twice, and store in a dry sterile bottle.
[0077] (2) Obtain axillary buds by inducing culture: clamp the above-mentioned sterilized aseptic explants with sterile tweezers, cut off the parts that contact the disinfectant at both ends, and leave a 1.0 cm long stem segment with 1 internode. The lower end of the morphology was obliquely inserted on the solid medium for inducing the germination of axillary buds, and placed in a da...
example 2
[0086] (1) Collection and disinfection of explants: On sunny days for 5 consecutive days, without watering the day before, cut the semi-lignified branches of the chrysanthemum chrysalis with ungerminated axillary buds, remove the leaves, and cut the segmented stems as explants. For the plant, use alcohol cotton balls with a mass concentration of 75% to wipe the stem explants for 2 times, then place them on the ultra-clean workbench, cut them into stems with 1 internode, and use 0.1% carbon dioxide Soak in chlorine for 20 minutes, rinse with sterile water three times, and store in a dry sterile bottle.
[0087] (2) Obtain axillary buds by inducing culture: clamp the above-mentioned sterilized aseptic explants with sterile tweezers, cut off the parts that contact the disinfectant at both ends, and leave a 1.0 cm long stem segment with 1 internode. The lower end of the morphology was obliquely inserted on the solid medium for inducing the germination of axillary buds, and placed ...
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