Efficient starting culture medium for directly inducing tetraploid paulownia large-field stem segment to re-grow adventitious buds, and application
A high-efficiency start-up and culture medium technology, applied in the biological field, can solve the problems of loss of excellent plant traits, reduction of reproduction coefficient, vitrification, etc., to achieve the effect of saving manpower and high reproduction coefficient
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Embodiment 1
[0022] Cut off the leaves of the tetraploid paulownia branches retrieved from the field, rinse the branches with tap water first, and then cut them into stems with 1 bud. Generally, the length of the stem is about 1.5 cm. After the disinfection treatment, inoculate on the stem initiation medium, the composition of the stem initiation medium is MS+6-BA 0.5mg / L+GA 0.05mg / L+KT 0.05mg / L+NAA0.05mg / L+agar 4.5 g / L+ sucrose 30g / L (pH value 5.8), culture conditions are daytime temperature 25°C, night temperature 18°C, light intensity 2500Lx, light time 13h / d. After culturing for about 20 days, the average proliferation coefficient reached 3.8. See figure 1 .
Embodiment 2
[0024] Cut off the leaves of the tetraploid paulownia branches retrieved from the field, rinse the branches with tap water first, and then cut them into stems with 1 bud. Generally, the length of the stem is about 1.5 cm. After the disinfection treatment, it was inoculated on the starting medium of the stem segment, and the composition of the starting medium of the stem segment was MS+6-BA4.0mg / L+GA1.0mg / L+KT 0.5mg / L+NAA1.0mg / L+agar 5.0 g / L + sucrose 40g / L (pH value 5.8), culture conditions are daytime temperature 25°C, night temperature 18°C, light intensity 2500Lx, light time 13h / d. After culturing for 20 days, the average proliferation coefficient reached 6.3. See figure 2 .
Embodiment 3
[0026] Cut off the leaves of the tetraploid paulownia branches retrieved from the field, rinse the branches with tap water first, and then cut them into stems with 1 bud. Generally, the length of the stem is about 1.5 cm. After the disinfection treatment, inoculate on the stem initiation medium, the composition of the stem initiation medium is MS+6-BA 14.0mg / L+GA 3.0mg / L+KT 3.0mg / L+NAA3.0mg / L+agar 6.0 g / L+sucrose 50g / L (pH 6.0), the culture conditions were daytime temperature 25°C, night temperature 18°C, light intensity 2500Lx, light time 13h / d. After culturing for 20 days, the average proliferation coefficient reached 4.7. See image 3 .
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