Breeding method of tomato disease-resisting homozygotes
A breeding method and homozygous technology, applied in the field of crop breeding, can solve problems such as low breeding success rate and long breeding cycle, and achieve the effects of increasing induction rate, increasing success rate, and improving stress resistance
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Embodiment 1
[0044] Tomato anthers were taken as explants, and 6 different medium treatments were set up, each of which was repeated 3 times. The specific technical scheme is as follows:
[0045] Treatment 1: Tomato anther haploid culture is carried out according to the method of the present invention.
[0046] Yu Qingtian collected 6-8 mm long flower buds from the disease-resistant tomato mutant plants in the greenhouse of the Shouguang Vegetable Group Breeding Base, which were pre-checked by pressing, and placed at 4°C for pretreatment for 4 days. The flower buds were sterilized with 75% alcohol for 30 seconds before inoculation, then with 0.1% mercuric chloride for 10 minutes, and then rinsed 4 times with sterile water. The anthers were taken out from the flower buds under sterile conditions, and the anthers with a length of 2-5 mm (the pollen development period in them was the mononuclear border stage) were selected for anther culture. The anthers were inoculated in MS basic medium, s...
Embodiment 2
[0073] Practical application: Tomato anther haploid culture is carried out according to the method of the present invention.
[0074] Yu Qingtian collected 6-8 mm long flower buds from disease-resistant mutant tomato plants in the greenhouse of Shouguang Vegetable Group Breeding Base, and placed them at 4°C for 4 days of pretreatment. The flower buds were sterilized with 75% alcohol for 30 seconds before inoculation, then with 0.1% mercuric chloride for 10 minutes, and then rinsed 4 times with sterile water. The anthers were taken out from the flower buds under sterile conditions, and the anthers with a length of 2-5 mm (the pollen development period in them was the mononuclear border stage) were selected for anther culture. The anthers were inoculated in MS basic medium, KT 0.5mg / L, 2,4-D 1mg / L, trehalose 30g / L, black fruit Lycium barbarum juice filtrate 20g / L and agar 8g / L, pH 5.8 culture base for callus induction culture. Culture conditions: 80% relative humidity, 24-26°C...
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