Method for producing chilli kernel male sterile plants in large scale
A male sterility, large-scale technology, applied in the fields of botanical equipment and methods, horticultural methods, plant regeneration, etc., can solve the problems of small reproduction coefficient, serious variation, and high labor cost, and achieve large reproduction coefficient, stable traits, The effect of less technical difficulty
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Embodiment 1
[0024] The large-scale tissue culture of capsicum genital male sterile line 2003A field plant, its steps are:
[0025] 1. The commercially available capsicum male sterile dual-purpose line 2003A is planted in open field farmland;
[0026] 2. During the flowering period, select one of the sterile plants, cut off the vigorously growing, pest-free branches, remove the leaves, cut the remaining branches into stems with a single node, sterilize them with 75% alcohol for 20 seconds, and then use Treat with bleaching powder for 25 minutes, then rinse with sterile water 4 times;
[0027] 3. Inoculate the sterile stem segments obtained through the above 2 steps on the axillary bud induction medium under artificially controlled environmental conditions, cultivate for 30 days, and induce the germination and growth of axillary buds; wherein, the axillary bud induction medium is: MS, and in it Add mass ratio: 3% sucrose, 0.6% agar, 0.5% benzyl adenine (BA), and 0.01% α-naphthyl acetic aci...
Embodiment 2
[0035] The large-scale tissue culture of capsicum genital male sterile dual-purpose line 0908A field plant, its steps are:
[0036] This example is basically the same as Example 1, except that the material used is the commercially available capsicum male sterile line 0908A; the axillary bud induction medium is MS, and the mass ratio of 2.0% benzyl base adenine, and 0.1% a-naphthyl acetic acid; the adventitious root induction medium for clustered shoots is: 1 / 2MS, and the content of ferrous salt therein is the same as that of MS medium, and in this 1 / 2MS medium, also contains The mass ratio is: 0.1% a-naphthalene acetic acid and 0.1% indolebutyric acid; the artificially controlled environmental conditions are: continuous light for 14 hours a day, temperature 26°C, light intensity 50umol.m -2 .s -1 The seedling hardening time is 10 days after removing the sealing film. The mixed substrate in the nutrient pot is: the volume ratio of perlite and peat soil is 2:1. After 20 days, t...
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