Monkshood-tuber tissue culture and rapid propagation method
A technology for tissue culture and A. chinensis, applied in the field of tissue culture and rapid propagation of A. chinensis, can solve problems such as low yield, poor disease resistance, instability, etc., achieve high differentiation rate and rooting rate, solve poor disease resistance, and survival rate. high effect
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Embodiment 1
[0030] In this embodiment, the shoot tip of the Aconite plant in Pingwu Aconite Provenance Base of Sichuan was selected as the explant, and the callus was induced by tissue culture for rapid propagation, including the following main steps:
[0031] Step 1: Selection and disinfection of explants
[0032] In the Sichuan Pingwu Fuzi Provenance Base, in March, the shoot tip of the annual robust Aconitum plant was selected as the explant (as the inoculation material), and treated at a low temperature of 4°C for 3 days; rinsed with tap water, and treated with 75% alcohol for 15-15 20s, soak in 0.1% mercury chloride solution for 10-12min, pour off the mercury solution, and wash with sterile water for 4-5 times; peel off the stem tip and cut it into 0.2mm length, and set aside;
[0033] The second step: inoculation and induction of callus
[0034] Use MS as the basic medium, add NAA 0.1mg / L+6-BA 1.0mg / L to the basic medium as the medium for inducing callus, and inoculate the explants...
Embodiment 2
[0046] In this embodiment, the leaves of Aconite fruticosa plants in Sichuan Pingwu Aconite Provenance Base are selected as explants, and rapid propagation is carried out through tissue culture, including the following main steps:
[0047] Step 1: Selection and disinfection of explants
[0048] In the Sichuan Pingwu Aconite Provenance Base, in March, the leaves of the annual robust Aconitum plant were selected as explants (as inoculation materials), treated at a low temperature of 4°C for 3 days; rinsed with tap water, and treated with 70% alcohol for 15-20s , soak in 0.1% mercuric acid solution for 10-12 minutes, pour off the mercuric solution, and wash it with sterile water for 4-5 times; cut the leaves into 1cm×1cm cubes and set aside;
[0049] Step 2: Induction of Callus
[0050] Use MS as the basic medium, add NAA 0.2mg / L+6-BA 4.0mg / L to the basic medium as the medium for inducing callus, and inoculate the explants treated in the first step above according to the convent...
Embodiment 3
[0062] In this embodiment, the stem section of the Aconite plant and the stem section with axillary buds in the Sichuan Pingwu Aconite Provenance Base are selected as explants, and the callus is induced by tissue culture for rapid propagation, including the following main steps:
[0063] Step 1: Selection and disinfection of explants
[0064] In the Sichuan Pingwu Fuzi Provenance Base, in March, the stem section of the annual strong Aconite plant and the stem section with axillary buds were selected as explants (as inoculation materials), treated at a low temperature of 4°C for 3 days; rinsed with tap water, Treat with 70% alcohol for 15-20 seconds, soak in 0.1% mercuric acid solution for 10-12 minutes, pour out the mercuric acid solution, and wash it with sterile water for 4-5 times; cut the stems and stems with axillary buds into about 1.5cm, stand-by;
[0065] The second step: inoculation and induction of callus
[0066] Use MS as the basic medium, add NAA 0.2mg / L+6-BA 2....
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