Cultivation method of chili disease-resistant homozygote
A cultivation method and homozygous technology, applied in the field of crop breeding, can solve the problems of low breeding success rate and long breeding cycle, and achieve the effects of improving induction rate, success rate and stress resistance.
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Embodiment 1
[0050] Take capsicum anther as explant, establish 6 kinds of different mediums to handle, each repeat 3 times, specific technical scheme is as follows:
[0051] Treatment 1: Carry out capsicum anther haploid culture according to the method of the present invention.
[0052] On sunny days, flower buds with a length of 4.0-4.49 mm were collected from pepper plants in the greenhouse of the Shouguang Vegetable Group Breeding Base, pretreated at 4°C for 4 days, added 3-4 drops of Tween 80, and rinsed in running water for 1.5 hours; % alcohol disinfection for 15 seconds, rinsed with sterile water 4 times; disinfected with 0.1% mercuric chloride (mercuric chloride) for 10 minutes, rinsed with sterile water 4 times. The anthers were inoculated on MS basic medium plus supplementary components, and the supplementary components were 0.05 mg·L -1 6-BA, 0.01mg·L -1 2,4-D, 30g·L -1 Trehalose, 20g·L -1 Black fruit wolfberry juice filtrate, 7g·L -1 Agar powder, pH5.8. The inoculation ...
Embodiment 2
[0078] Practical application: Carry out capsicum anther haploid culture according to the method of the present invention.
[0079] Collect flower buds with a length of 4.0-4.49 mm from pepper plants in the greenhouse of Shouguang Vegetable Group Breeding Base on a sunny day, pretreat them at 4°C for 4 days, add 4 drops of Tween 80, and rinse them in running water for 1.5 hours; then use 75% alcohol Disinfect for 15 seconds, rinse with sterile water 4 times; disinfect with 0.1% mercuric chloride (mercuric chloride) for 10 minutes, rinse with sterile water 4 times. The anthers were inoculated on MS basic medium, and the medium formula was 0.05 mg·L -1 6-BA, 0.01mg·L -1 2,4-D, 30g·L -1 Trehalose, 20g·L -1 Black fruit wolfberry juice filtrate, 7g·L -1 Agar powder, pH 5.8. The inoculation density was 8 flower buds per 100 mm Petri dish. Then continue culturing in a tissue culture room with a temperature of 28°C during the day and a temperature of 20°C at night.
[0080] Wh...
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