Reproduction method for tissue culture of amorphophallus bulbifer
A technology of tissue culture and konjac, which is applied in the field of plant cell engineering, can solve the problems of rapid propagation technology research of unjin konjac varieties, long bulb cycle of bulbil konjac bulbs, and low bulb reproduction coefficient, so as to achieve quality that is not easily degraded, vitality and Strong stress resistance and large single grain diameter
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Embodiment 1
[0022] A kind of propagation method related to the tissue culture of bulbil Amorphophallus konjac, comprising the steps of aseptic seedling culture, embryoid body induction, seed bulb induction, and seed bulb maturation culture:
[0023] 1) Sterile seedling cultivation: After the young leaves, petioles and clustered buds of the bulbil class konjac plants are routinely sterilized, the leaves are cut into 0.5-1.0cm2, the petioles are cut into 0.8-1cm long, and inoculated into conventionally sterilized seedlings On the culture medium, culture under 2000lux light, 11h / d, culture temperature 28±1℃, to obtain virus-free and sterile seedlings; the composition and ratio of the seedling medium are: MS basic medium + 0.2mg / L NAA + 0.5 mg / L 6-BA+activated carbon 0-3.0g / L, sucrose 30g / L, agar 6-8g / L, adjust the pH to 5.8-6.2;
[0024] 2) embryoid body induction: the detoxified aseptic seedlings obtained in step 1), get the leaves and cut them into 0.5-1.0cm 2, cut the petioles into 0.8-1....
Embodiment 2
[0034] A kind of propagation method related to the tissue culture of bulbil Amorphophallus konjac, comprising the steps of aseptic seedling culture, embryoid body induction, seed bulb induction, and seed bulb maturation culture:
[0035] 1) Sterile seedling cultivation: After the young leaves, petioles and clustered buds of the bulbil class konjac plants are routinely sterilized, the leaves are cut into 0.5-1.0cm2, the petioles are cut into 0.8-1cm long, and inoculated into conventionally sterilized seedlings On the culture medium, culture under 2000lux light, 11h / d, culture temperature 28±1℃, to obtain virus-free and sterile seedlings; the composition and ratio of the seedling medium are: MS basic medium + 0.2mg / L NAA + 0.5 mg / L 6-BA+activated carbon 0-3.0g / L, sucrose 30g / L, agar 6-8g / L, adjust the pH to 5.8-6.2;
[0036] 2) embryoid body induction: the detoxified aseptic seedlings obtained in step 1), get the leaves and cut them into 0.5-1.0cm 2, cut the petioles into 0.8-1....
Embodiment 3
[0047] A kind of propagation method related to the tissue culture of bulbil Amorphophallus konjac, comprising the steps of aseptic seedling culture, embryoid body induction, seed bulb induction, and seed bulb maturation culture:
[0048] 1) Sterile seedling cultivation: After the young leaves, petioles and clustered buds of the bulbil class konjac plants are routinely sterilized, the leaves are cut into 0.5-1.0cm2, the petioles are cut into 0.8-1cm long, and inoculated into conventionally sterilized seedlings On the culture medium, culture under 2000lux light, 11h / d, culture temperature 28±1℃, to obtain virus-free and sterile seedlings; the composition and ratio of the seedling medium are: MS basic medium + 0.2mg / L NAA + 0.5 mg / L 6-BA+activated carbon 0-3.0g / L, sucrose 30g / L, agar 6-8g / L, adjust the pH to 5.8-6.2;
[0049] 2) embryoid body induction: the detoxified aseptic seedlings obtained in step 1), get the leaves and cut them into 0.5-1.0cm 2, cut the petioles into 0.8-1....
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