Method for tissue culture and rapid propagation of stems of cinnamomum kanehirae hay
A technology of tissue culture rapid propagation and camphor, which is applied in the field of plant tissue culture, can solve the problems of immature technology, inability to carry out large-scale breeding, low survival rate, etc., and achieve the goal of reducing dryness and death, normal shape, and reducing pollution rate Effect
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Embodiment 1
[0042] Example 1 Influence of different disinfectant treatment and disinfection time on the disinfection effect of Cinnamomum camphora stem
[0043] Collect the young side branches with full axillary buds of the healthy mother tree that have not yet germinated, remove the leaves and keep 1~2 cm petioles, cut into 4~6 cm long stems, first soak in washing powder water for 30 min, and then use 1000 Soak in mg / L thiophanate-methyl for 10 min (blank: when not soaking in 1000 mg / L thiophanate-methyl, rinse with running water for 30 min instead). Soak in 75% alcohol for 30 s on the ultra-clean workbench, rinse with sterile water 3 times, then treat with 0.1% mercury liters for 5-15 minutes, and rinse with sterile water 4-6 times. The ends and petioles were cut off 1 cm each, and cut into stem segments with 1-2 axillary buds, and inoculated on the spare medium.
[0044] Each treatment was inoculated with 30 shoots and stems, and the experiment was repeated 3 times. Thirty days after the...
Embodiment 2
[0051] Example 2 Effect of Different Induction Medium on Induction of Cinnamomum Cinnamomum Stem
[0052] According to the disinfection method in Example 1, collect the young side branches with full axillary buds of the healthy mother tree that have not yet germinated, remove the leaves and retain 1~2 cm petioles, cut into 4~6 cm long stems, first use washing powder Soak in water for 30 min, and then soak with 1000 mg / L thiophanate methyl for 10 min. Soak in 75% alcohol for 30 s on the ultra-clean workbench, rinse 3 times with sterile water, then rinse with 0.1% mercury for 10 min, rinse 4-6 times with sterile water. The ends and petioles were cut off 1 cm each, and cut into stem segments with 1-2 axillary buds, and inoculated in the following induction medium (see Table 2 for the specific formulation of the induction medium) for bud induction culture. The cultivation light intensity is 1500-2000 lux, and the light time is 12 hours / day.
[0053] The induction medium is compose...
Embodiment 3
[0060] Example 3 Effect of Different Proliferation Medium on Proliferation and Culture of Cinnamomum camphora
[0061] The shoots induced in Example 2 were inoculated into a proliferation medium (see Table 3 for the specific formula of the proliferation medium) for proliferation culture. The cultivation light intensity is 1500-2000 lux, and the light time is 12 hours / day.
[0062] The proliferation medium is composed of a combination of a basic medium and hormones, and the basic medium includes the following components: MS medium, Vc 2.0 mg / L, biotin 0.30 mg / L, and L-cysteine 5.0 mg / L L, sucrose 30g / L, agar 7 g / L, pH 5.8.
[0063] For each treatment, 40 shoots were inoculated, and the experiment was repeated 3 times. For each generation of bud proliferation and cultivation (ie every 30 days), the corresponding proliferation coefficient and bud growth are calculated.
[0064] Table 3 Effects of different hormone combinations on the proliferation of Cinnamomum camphora buds
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