Induction culture medium for tomato tissue culture, tissue culture method and application
A technology for inducing medium and tissue culture, applied in the directions of application, horticultural methods, botanical equipment and methods, etc., can solve the problems of water resources and fertilizer waste, quality decline, and high incidence of vegetable disease
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Embodiment 1
[0045] Cultivation of tomato tissue culture seedlings
[0046] The tomato tissue culture process is carried out in a culture room. Set the culture temperature of the tissue culture room at 25 °C, the humidity at 50%, the light intensity at 2000 Lx, the light period of 16 hours, and the dark period of 8 hours.
[0047] Prepare the medium according to the following recipe:
[0048] Induction medium: MS basic medium + 3-indoleacetic acid 0.04mg / L+6-benzylaminoadenine 1.0mg / L+ methyl jasmonate 1.5mg / L+ polyvinylpyrrolidone 5mg / L+ agar 5g / L+ sucrose 30g / L; pH value is 6.0;
[0049] Rooting medium: MS basic medium + indole butyric acid 0.8 mg / L + agar 5 g / L + sucrose 30 g / L.
[0050] The leaves of Jingdan No. 1 tomato were used as explants, rinsed thoroughly with tap water, then soaked in 5% Tween-20 for 5 minutes, rinsed 3-4 times with sterilized distilled water, 0.1% mercuric chloride (HgCl 2 ) Surface sterilize for 4 minutes, rinse 4-5 times with sterile distilled water. Th...
Embodiment 2
[0052] Cultivation of tomato tissue culture seedlings
[0053] The tomato tissue culture process is carried out in a culture room. Set the tissue culture room culture temperature to 24 °C, humidity to 55%, light intensity to 2500 Lx, 15-hour photoperiod, and 9-hour dark period.
[0054] Prepare the medium according to the following recipe:
[0055] Induction medium: MS basic medium+ 3-indoleacetic acid 0.05mg / L+6-benzylaminoadenine 1.5mg / L+ methyl jasmonate 2.5mg / L+ polyvinylpyrrolidone 8mg / L+ agar 7g / L+ sucrose 35g / L, the pH value is 5.5;
[0056] Rooting medium: MS basic medium + indole butyric acid 1.0 mg / L + agar 8 g / L + sucrose 35 g / L.
[0057] The leaves of Jingdan No. 1 tomato were used as explants, rinsed thoroughly with tap water, then soaked in 5% Tween-20 for 6 minutes, rinsed 3-4 times with sterilized distilled water, 0.1% mercuric chloride (HgCl) 2 ) Surface sterilize for 4 minutes, rinse 4-5 times with sterile distilled water. The leaf tissue was cut into a...
Embodiment 3
[0059] Cultivation of tomato tissue culture seedlings
[0060] The tomato tissue culture process is carried out in a culture room. Set the tissue culture room culture temperature to 26 °C, humidity to 60%, light intensity to 3000 Lx, 14-hour photoperiod, and 10-hour dark period.
[0061] Prepare the medium according to the following recipe:
[0062] Induction medium: MS basic medium+ 3-indoleacetic acid 0.02mg / L+6-benzylaminoadenine 0.8mg / L+ methyl jasmonate 3.7mg / L+ polyvinylpyrrolidone 10 mg / L+ agar 8g / L+ sucrose 40g / L, pH value is 6.5;
[0063] Rooting medium: MS basic medium + indole butyric acid 1.2 mg / L + agar 10 g / L + sucrose 40 g / L.
[0064] The leaves of Jingdan No. 1 tomato were used as explants, rinsed thoroughly with tap water, then soaked in 5% Tween-20 for 8 minutes, rinsed 3-4 times with sterilized distilled water, 0.1% mercuric chloride (HgCl) 2 ) Surface sterilize for 4 minutes, rinse 4-5 times with sterile distilled water. The leaf tissue was cut into a...
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