Peony in vitro culture brown stain prevention rooting promoting agent
An in vitro culture and anti-browning agent technology, which is applied in plant regeneration, horticulture, botany equipment and methods, etc., can solve the problems of low reproduction coefficient, difficulty in achieving standardized large-scale production, and large individual differences
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Embodiment 1
[0016] An anti-browning and rooting-promoting agent for in vitro culture of peony, the components of which include by weight: 1 part of 6-benzylaminopurine, 0.05 part of indole-3-acetic acid, 0.5 part of diethyl hexanoate, and 35 parts of an anti-browning agent , 100 parts of activated carbon, 15 parts of indole butyric acid, 25 parts of carbon source.
Embodiment 2
[0018] An anti-browning and root-promoting agent for in vitro culture of peony, the components of which include by weight: 1 part of 6-benzylaminopurine, 0.1 part of indole-3-acetic acid, 1 part of diethyl diethylhexanoate, and 28 parts of anti-browning agent , 80 parts of activated carbon, 12 parts of indole butyric acid, 20 parts of carbon source;
[0019] Wherein, the anti-browning agent includes vitamin C and riboflavin; the mass ratio of vitamin C to riboflavin is 2:3; the carbon source is sucrose; the concentration of the sucrose is 20g / L; The cultivation temperature of the root-promoting agent is 24° C.; the pH value of the culture medium using the root-promoting agent is 6.0.
Embodiment 3
[0021] An anti-browning root-promoting agent for in vitro culture of peony, the components of which include by weight: 0.5 parts of 6-benzylaminopurine, 0.05 parts of indole-3-acetic acid, 2 parts of diethyl diethylhexanoate, and 35 parts of anti-browning agent , 50 parts of activated carbon, 10 parts of indole butyric acid, 30 parts of carbon source;
[0022] Wherein, the anti-browning agent includes vitamin C and riboflavin; the mass ratio of vitamin C and riboflavin is 3:4; the carbon source is sucrose; the concentration of the sucrose is 30g / L; The culture temperature of the root-promoting agent is 23° C.; the pH value of the culture medium using the root-promoting agent is 6.2.
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