A kind of breeding method of tomato disease-resistant homozygous
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 the survival rate, weak photosynthetic autotrophic ability, and improving the survival rate of seedlings.
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Embodiment 1
[0044] Take tomato anthers as explants, set up 6 kinds of different mediums to deal with, each repeat 3 times, the specific technical scheme is as follows:
[0045] Treatment 1: Carry out tomato anther haploid culture according to the method of the present invention.
[0046] On a sunny day, 6-8 mm long flower buds selected from the disease-resistant tomato mutant plants in the greenhouse of the breeding base of Shouguang Vegetable Group were collected and pretreated at 4°C for 4 days. Before inoculation, the flower buds were sterilized with 75% alcohol for 30 seconds, then sterilized with 0.1% mercuric chloride for 10 minutes, and then washed 4 times with sterile water. The anthers were taken out from the flower buds under aseptic conditions, and the anthers with a length of 2-5 mm (the pollen development period in them was the uninucleate marginal stage) were selected for anther culture. Inoculate the anthers on MS basic medium, add KT 0.5mg / L, 2,4-D 1mg / L, trehalose 30g / L,...
Embodiment 2
[0073] Practical application: Carry out tomato anther haploid culture according to the method of the present invention.
[0074] On sunny days, flower buds with a length of 6-8 mm were collected from the disease-resistant tomato mutant plants in the greenhouse of the Shouguang Vegetable Group Breeding Base, and pretreated at 4°C for 4 days. Before inoculation, the flower buds were sterilized with 75% alcohol for 30 seconds, then sterilized with 0.1% mercuric chloride for 10 minutes, and then washed 4 times with sterile water. The anthers were taken out from the flower buds under aseptic conditions, and the anthers with a length of 2-5 mm (the pollen development period in them was the uninucleate marginal stage) were selected for anther culture. The anthers were inoculated on MS basic medium, KT0.5mg / L, 2,4-D 1mg / L, trehalose 30g / L, black wolfberry juice filtrate 20g / L and agar 8g / L, pH 5.8 callus induction culture. Culture conditions: relative humidity 80%, 24-26°C, light in...
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