A method for reducing the browning rate of leaf tissue culture of Begonia variegata
A technology for tissue culture and begonia, applied in the field of plant tissue culture, can solve the problems of limiting the tissue culture efficiency and browning of begonia variegata, and achieve the effects of reducing pollution rate and browning rate, eliminating browning, and increasing induction rate
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Embodiment 1
[0025] A method for reducing the browning rate of begonia iridescent leaf tissue culture, comprising the steps of:
[0026] Step (1), refrigerated preservation treatment: refrigerated fresh young leaves of Begonia variegata in a refrigerator at 4°C for 1 day;
[0027] Step (2), disinfection and treatment of explants: After washing the young leaves treated in step (1) with washing powder water, soak them in alcohol with a volume concentration of 75% for 30 seconds, and then wash them with 0.1% HgCl 2 The solution was treated for 5 minutes, followed by rinsing with sterile water for 3 times; then under aseptic conditions, the water was absorbed with sterile filter paper, and then the leaves were cut into 2cm 2 size leaf disk;
[0028] Step (3), dark culture: scratch the back of the leaf disc obtained in step (2), inoculate the primary culture medium with the back of the leaves facing down, and culture in the dark for 5 days at a culture temperature of 23±2°C;
[0029] Step (4)...
Embodiment 2
[0034] A method for reducing the browning rate of begonia iridescent leaf tissue culture, comprising the steps of:
[0035] Step (1), refrigerated preservation treatment: refrigerated fresh young leaves of Begonia variegata in a refrigerator at 4°C for 2 days;
[0036] Step (2), disinfection and treatment of explants: After washing the young leaves treated in step (1) with washing powder water, soak them in alcohol with a volume concentration of 75% for 30 seconds, and then wash them with 0.1% HgCl 2 The solution was treated for 8 minutes, and then rinsed with sterile water for 3 times, each time for 2 minutes; then under sterile conditions, use sterile filter paper to absorb water, and then cut the leaves into 2cm 2 size leaf disk;
[0037] Step (3), dark culture: scratch the back of the leaf disc obtained in step (2), inoculate the primary culture medium with the back of the leaves facing down, and culture in the dark for 5 days at a culture temperature of 23±2°C;
[0038]...
Embodiment 3
[0043] A method for reducing the browning rate of begonia iridescent leaf tissue culture, comprising the steps of:
[0044] Step (1), refrigerated preservation treatment: refrigerated fresh young leaves of Begonia variegata in a refrigerator at 4°C for 1 day;
[0045] Step (2), disinfection and treatment of explants: After washing the young leaves treated in step (1) with washing powder water, soak them in alcohol with a volume concentration of 70% for 20 seconds, and then wash them with 0.1% HgCl 2 The solution was treated for 5 minutes, then rinsed with sterile water for 3 times, each time for 2 minutes; then under sterile conditions, use sterile filter paper to absorb water, and then cut the leaves into 1.8cm 2 size leaf disk;
[0046] Step (3), dark culture: scratch the back of the leaf disc obtained in step (2), inoculate the primary culture medium with the back of the leaves facing down, and culture in the dark for 5 days at a culture temperature of 23±2°C;
[0047] St...
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