A kind of method of ginger tissue culture
A tissue culture and ginger technology, applied in the field of ginger tissue culture, can solve the problems of easy browning of callus, low survival rate, low reproduction coefficient, etc., achieves improvement of survival rate and detoxification rate, simplification of tissue culture steps, proliferation The effect of increasing the coefficient
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Embodiment 1
[0029] A method for rapid propagation of ginger by tissue culture, characterized in that, proceed as follows:
[0030]Pretreatment: take a ginger stem tip with a size of 0.6 cm, infiltrate it with ethanol with a volume concentration of 70% for 30 seconds, then wash it with sterile water, repeat the same ethanol infiltration once, wash it with sterile water, and heat it at 50°C 5min;
[0031] Inoculation
[0032] (1) Inoculate ginger shoot tips after pretreatment in slow-release medium and carry out primary culture, and described slow-release medium is to supplement 6-BA 0.5mg / L, NAA slow-release auxin 2mg / L in MS basal medium , TDZ 0.3mg / L, 2% sucrose, agar 0.55%, adjust the pH to 5.8;
[0033] Among them, NAA sustained-release auxin is made of nano-SiO 2 Disperse in de-ethanol ionized aqueous solution, add NAA, then add PVP k30, mix and heat to 80°C for 30 minutes, stop heating, cool to room temperature, then filter and dry to obtain SiO 2 , The mass ratio of NAA and PVP ...
Embodiment 2
[0036] A method for rapid propagation of ginger by tissue culture, characterized in that, proceed as follows:
[0037] Pretreatment: take a ginger stem tip with a size of 0.8 cm, soak it with ethanol with a volume concentration of 70% for 40 seconds, then wash it with sterile water, repeat the same soaking with ethanol once, wash it with sterile water, and heat it at 50°C 8min;
[0038] Inoculation
[0039] (1) Inoculate ginger shoot tip after pretreatment in slow-release medium and carry out primary culture, and described slow-release medium is to supplement 6-BA 1.5mg / L, NAA slow-release auxin 3mg / L in MS basal medium , TDZ 0.25mg / L, 2% sucrose, agar 0.65%, adjust the pH to 6;
[0040] Among them, NAA sustained-release auxin is made of nano-SiO 2 Disperse in de-ethanol ionized aqueous solution, add NAA, then add PVP k30, mix and heat to 90°C for 20 minutes, stop heating, cool to room temperature, then filter and dry to obtain SiO 2 , The mass ratio of NAA and PVP k30 is ...
Embodiment 3
[0043] A method for rapid propagation of ginger by tissue culture, characterized in that, proceed as follows:
[0044] Pretreatment: take a ginger stem tip with a size of 0.7 cm, soak it with ethanol with a volume concentration of 70% for 35 seconds, then wash it with sterile water, repeat the same soaking with ethanol once, wash it with sterile water, and heat it at 50°C 6min;
[0045] Inoculation
[0046] (1) Ginger stem tip after pretreatment is inoculated in slow-release medium and carries out primary culture, and described slow-release medium is to supplement 6-BA 1mg / L, NAA slow-release auxin 2.5mg / L in MS basal medium , TDZ 0.28mg / L, 2% sucrose, agar 0.6%, adjust the pH to 5.8;
[0047] Among them, NAA sustained-release auxin is made of nano-SiO 2 Disperse in de-ethanol ionized aqueous solution, add NAA, then add PVP k30, mix and heat to 85°C for 25min, stop heating, cool to room temperature, then filter and dry to obtain SiO 2 , The mass ratio of NAA and PVP k30 is...
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