Method for creating zoysia japonica mutant by utilizing oxygen cold plasma mutagenesis
A technology of cold plasma and zoysia, applied in gardening methods, botanical equipment and methods, applications, etc., can solve the problems of slow growth of zoysia, long breeding cycle, hindering zoysia, etc., and achieve charged ion The effect of increasing the species and concentration of active particles, accelerating the breeding process, and broad application prospects
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Embodiment 1
[0038] Get the young tiller buds ( figure 2 ), 15% H 2 o 2 Soak for 15 minutes, rinse with distilled water for 3 minutes, then soak in 50% alcohol for 8 minutes, rinse with distilled water for 10 minutes, sterilize and then inoculate into induction medium (medium formula: MS medium, add 2,4-D 6mg / L, L-proline 4g / L, 5-aminolevulinic acid 5mg / L, VB 1 2mg / L, sucrose 25g / L and phytogel 3g / L), cultivated in the dark at 25±1°C for 30d, and obtained Zoysia somatic tissue.
[0039] Take 5 granular somatic tissues with a diameter of 0.4 cm and place them in figure 1 In the quartz glass petri dish with an inner diameter of 6 cm in the cold plasma discharge device shown, place the petri dish between the two plates of radio frequency discharge, the distance from the electrode plates is 1 cm, close the reaction system, evacuate, and feed oxygen for 10 minutes. The pressure is 15Pa, the processing power is 650W, and the mutagenesis is 8min.
[0040] The cold plasma treated somatic tis...
Embodiment 2
[0047] Get the young and tender tiller buds of Zoysia rugosa with a length of 1 cm, and use 15% H 2 o 2 Soak for 15 minutes, rinse with distilled water for 5 minutes, then soak with 50% alcohol for 8 minutes, rinse with distilled water for 10 minutes, and inoculate the sterilized tiller buds into induction medium (MS medium, 2,4-D 8mg / L, L-proline 5g / L L, 5-aminolevulinic acid 7mg / L, VB 1 3mg / L, sugarcane 30g / L and plant gel 5g / L), cultured in the dark at 25±1°C for 30d to obtain Zoysia somatic cells.
[0048] Take 5 granular somatic tissues with a diameter of 0.7cm, place them in a quartz glass petri dish with a diameter of 6cm, place the petri dish between the two polar plates of radio frequency discharge, and the distance from the electrode plates is 2cm, and seal the reaction system. Vacuumize, feed oxygen for 12min, pressure is 30Pa, processing power is 750W, mutagenesis is 12min. The cold plasma-treated somatic tissue was inoculated into differentiation medium (MS med...
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