Efficient and rapid tissue culture propagation method of konjac
A konjac and tissue culture technology, applied in the field of efficient and rapid tissue culture and propagation of konjac, can solve the problems of high cost of full-factory fast propagation, inability to connect with the market, and large reproduction coefficient, and achieves wide and sufficient materials, which is conducive to the production of improved varieties and the The effect of promotion and large reproduction coefficient
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Embodiment 1
[0048] A kind of konjac efficient rapid tissue culture propagation method, the method comprises the following steps:
[0049] 1) Preparation of medium: MS medium was used as the basic medium, 2.5mg / L of 6-benzylaminopurine, 2.0mg / L of α-naphthaleneacetic acid, 0.5mg / L of polyvinylpyrrolidone, 30g / L of sucrose, and agar After 6.5g / L, a callus induction medium with a pH value of 5.8-6.0 was prepared,
[0050] Prepared by using MS medium as the basic medium, adding 3.5mg / L 6-benzylaminopurine, 1.2mg / L α-naphthaleneacetic acid, 0.5mg / L polyvinylpyrrolidone, 30g / L sucrose, and 6.5g / L agar Bud differentiation induction medium with a pH value of 5.8-6.0,
[0051] Use 1 / 2 MS medium as the basic medium, add 3-indolebutyric acid 0.02mg / L, sucrose 30g / L, and agar 6.5g / L to prepare a rooting medium with a pH value of 5.8-6.0;
[0052] 2) Collection of konjac explants: collecting healthy, disease-free and uninjured 2 to 3-year-old konjac bulbs as explants;
[0053] 3) disinfection of ko...
Embodiment 2
[0061] A kind of konjac efficient rapid tissue culture propagation method, the method comprises the following steps:
[0062] 1) Preparation of medium: MS medium was used as basic medium, 0.6mg / L of 6-benzylaminopurine, 0.6mg / L of α-naphthaleneacetic acid, 0.5mg / L of polyvinylpyrrolidone, 30g / L of sucrose, agar After 6.5g / L, a callus induction medium with a pH value of 5.8-6.0 was prepared,
[0063] Prepared by using MS medium as the basic medium, adding 1.5mg / L of 6-benzylaminopurine, 0.5mg / L of α-naphthaleneacetic acid, 0.5mg / L of polyvinylpyrrolidone, 30g / L of sucrose, and 6.5g / L of agar Bud differentiation induction medium with a pH value of 5.8-6.0,
[0064] Use 1 / 2 MS medium as the basic medium, add 3-indolebutyric acid 0.02mg / L, sucrose 30g / L, and agar 6.5g / L to prepare a rooting medium with a pH value of 5.8-6.0;
[0065] 2) Collection of konjac explants: collecting healthy, disease-free and uninjured 2 to 3-year-old konjac bulbs as explants;
[0066] 3) disinfectio...
Embodiment 3
[0074] A kind of konjac efficient rapid tissue culture propagation method, the method comprises the following steps:
[0075] 1) Preparation of medium: MS medium was used as basic medium, 2.0mg / L of 6-benzylaminopurine, 2.0mg / L of α-naphthaleneacetic acid, 0.5mg / L of polyvinylpyrrolidone, 30g / L of sucrose, agar After 6.5g / L, a callus induction medium with a pH value of 5.8-6.0 was prepared,
[0076] Prepared by using MS medium as the basic medium, adding 1.0mg / L of 6-benzylaminopurine, 0.1mg / L of α-naphthaleneacetic acid, 0.5mg / L of polyvinylpyrrolidone, 30g / L of sucrose, and 6.5g / L of agar Bud differentiation induction medium with a pH value of 5.8-6.0,
[0077] Use 1 / 2 MS medium as the basic medium, add 3-indolebutyric acid 0.02mg / L, sucrose 30g / L, and agar 6.5g / L to prepare a rooting medium with a pH value of 5.8-6.0;
[0078] 2) Collection of konjac explants: collecting healthy, disease-free and uninjured 2 to 3-year-old konjac bulbs as explants;
[0079] 3) disinfectio...
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