A kind of in vitro culture and rapid propagation method of mantle orchid
A technology of in vitro culture and Trifolium pratense, applied in the field of plant tissue culture, can solve the problems of not being widely developed and applied, low reproductive efficiency, sharp reduction in quantity, etc. Effect
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Embodiment 1
[0021] (1) Collection of explants: In the spring of 2013, when new buds germinated, select robust cylindrica plants without obvious diseases in the field, use a scalpel to cut the newly-born vegetative buds with unopened leaf sheaths from the base, and perform simple water retention and moisturizing treatments Then bring it back to the laboratory for disinfection treatment in time.
[0022] (2) Induction of rhizomes: Rinse the explants overnight under running water, peel off the outer leaf sheaths until only two leaf sheaths are left, and place them on a clean bench and sterilize them in 0.1% mercury solution for 5 minutes. After washing twice with sterile water, peel off a layer of leaf sheath, and then put it in 0.1% mercury solution for disinfection for 1 minute. After rinsing with sterile water for 3 times, peel off the last layer of leaf sheath and rinse with sterile water for 5 times. Use sterile filter paper to absorb the water on the surface of the explant, and cut the ex...
Embodiment 2
[0030] (1) Explant collection: In the spring of 2014, when the sprouts of Phyllanthus spp. sprout, select robust plants with no obvious diseases in the field, use a scalpel to cut the newly-born nutrient buds with unopened leaf sheaths from the base, and perform water retention and moisturizing treatments in time Take it back to the laboratory for disinfection.
[0031] (2) Induction of rhizomes: Rinse the explants overnight under running water, peel off the outer leaf sheaths until only two leaf sheaths remain, and place them on a clean bench and sterilize them in a 0.1% mercury solution for 8 minutes. After rinsing with sterile water twice, peel off a layer of leaf sheath, and then put it in a 0.1% mercury solution for disinfection for 2 minutes. After rinsing with sterile water for 4 times, peel off the last layer of leaf sheath and rinse with sterile water for 6 times. Use sterile filter paper to absorb the water on the surface of the explant, and cut the explant into 0.3~0.5...
Embodiment 3
[0039] (1) Explant collection: In the spring of 2015, when the sprouts of Phyllanthus sp Take it back to the laboratory for disinfection.
[0040] (2) Induction of rhizomes: Rinse the explants overnight under running water, peel off the outer leaf sheaths until only two leaf sheaths are left, and place them on a clean bench and sterilize them in a 0.1% mercury solution for 10 minutes. After rinsing with sterile water 3 times, peel off a layer of leaf sheath, and then put it in 0.1% mercury solution for 3 minutes. After rinsing with sterile water for 5 times, peel off the last layer of leaf sheath and rinse with sterile water for 7 times. Use sterile filter paper to absorb the water on the surface of the explant, and cut the explant into 0.3~0.5 lengthwise with a sterile scalpel. The shoot point of about cm is inoculated into the induction medium and cultured in the dark for 120 days to induce the formation of rhizomes with a length of about 2 to 3 cm. The pollution rate is less ...
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