Method for producing lycoris by plant tissue culture
A technology for plant tissue culture and lycoris, which is applied to the field of plant tissue culture, can solve the problems of unfavorable quality continuation and development, low reproduction rate of lycoris, and pathogens, and achieves easy automatic control, expansion of reproduction, and short growth cycle. Effect
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Embodiment 1
[0021] Embodiment one: a kind of method adopting plant tissue culture lycoris, comprises the following steps:
[0022] (1) Preparation of medium: MS medium (Murashige and Skoog, 1962) was selected as the basic medium, and 2,4-D, IAA, NAA, 6-BA and IBA were used as regulated growth hormones to prepare three kinds of medium respectively : Bulb induction medium A: MS+NAA mg / L+2, 4-D 0.2mg / L+6-BA 1.0mg / L, rooting medium B: MS+IAA 0.1mg / L+IBA 0.1mg / L , medium C: MS+IAA 0.1mg / L; 20g / L sucrose and 4g / L agar were added to medium A and B, 15g / L sucrose and 1g / L agar were added to medium C, and 1mol L -1 Adjust the pH to 5.8 with NaOH and HCL, and sterilize the medium A, B and C in a high-pressure steam sterilizer at 0.1MPa and 121°C for 15min;
[0023] (2) Disinfection of explants: select Lycoris bulbs as explants, wash them with tap water for 1 hour, disinfect them with 0.5% 84 for 4 minutes on the aseptic operating table, rinse them with sterile water for 4 times, and then wash them...
Embodiment 2
[0028]Embodiment two: a kind of method adopting plant tissue culture Lycoris, comprises the following steps:
[0029] (1) Preparation of medium: MS medium (Murashige and Skoog, 1962) was selected as the basic medium, and 2,4-D, IAA, NAA, 6-BA and IBA were used as regulated growth hormones to prepare three kinds of medium respectively : Bulb induction medium A: MS+NAA 2.0mg / L+2,4-D 1.0mg / L+6-BA 5.0mg / L, rooting medium B: MS+IAA 1.0mg / L+IBA 1.0mg / L L, medium C: MS+IAA 1.0mg / L; 35g / L sucrose and 5g / L agar were added to medium A and B, 25g / L sucrose and 2g / L agar were added to medium C, and 2mol· L -1 NaOH and HCL to adjust the pH to 6.0, and sterilize the medium A, B and C in a high-pressure steam sterilizer at 0.15MPa and 125°C for 20min;
[0030] (2) Disinfection of explants: choose Lycoris bulbs as explants, wash them with tap water for 2 hours, disinfect them with 1% 84 for 2 minutes on the aseptic operating table, rinse them twice with sterile water, and then wash them wit...
Embodiment 3
[0035] Embodiment three: a kind of method adopting plant tissue culture Lycoris, comprises the following steps:
[0036] (1) Preparation of medium: MS medium (Murashige and Skoog, 1962) was selected as the basic medium, and 2,4-D, IAA, NAA, 6-BA and IBA were used as regulated growth hormones to prepare three kinds of medium respectively : Bulb induction medium A: MS+NAA 0.6mg / L+2, 4-D 0.3mg / L+6-BA 1.2mg / L, rooting medium B: MS+IAA 0.5mg / L+IBA 0.2mg / L L, medium C: MS+IAA 0.2mg / L; medium A and B were supplemented with 25g / L sucrose and 4.5g / L agar, medium C was supplemented with 16g / L sucrose and 1.2g / L agar, used 1.2mol·L -1 NaOH and HCL to adjust the pH to 5.9, and sterilize the medium A, B and C in a high-pressure steam sterilizer at 0.12MPa and 122°C for 16min;
[0037] (2) Disinfection of explants: select Lycoris bulbs as explants, wash them with tap water for 1.2 hours, disinfect them with 0.6% 84 for 3 minutes on the sterile operating table, rinse them with sterile wate...
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