Method for improving salt-tolerant properties of Brassicaceae crops
A technology of cruciferous crops and salt tolerance, which is applied in botany equipment and methods, horticultural methods, plant genetic improvement, etc., and can solve the problem of less research on salt tolerance
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Embodiment 1
[0075] Example 1: Salt tolerance treatment and germination screening of cabbage seeds
[0076] Carefully select green vegetable seeds with full grains and complete seed coats, and add a drop of 0.1% HgCl of Tuwen-20 2 After 10 minutes of sterilization, rinse with sterile water and dry the water, soak the seeds in a dark incubator at 25°C for 24 hours with 120mg / L Pingyangmycin at a dosage of 1ml / grain, take it out and rinse with sterile water Clean, inoculate on 1 / 2MS medium containing 0.8% NaCl, add 30g / L sucrose, 6.5g / L agar, pH 5.6, culture at 25±1°C, 10-12 hours of light per day, 5 After ~7 days, select the seeds that can germinate normally and have true leaves drawn out as the primary strains for salt-tolerant germination.
Embodiment 2
[0077] Example 2: Initial in vitro screening of salt-tolerant strains
[0078] Cut off the above-mentioned buds from which the true leaves have been extracted, inoculate them in 1 / 2MS medium with 30g / L sucrose, 6.5g / L agar, and pH 5.6, and cultivate them at 25±1°C with 10-12 hours of light per day After 20 to 25 days, when it grows to 4 to 5 true leaves, remove the glass seedlings and abnormal seedlings with abnormal true leaves, cut off the normal growing buds together with 4 true leaves, transfer them to 0.8% NaCl, add sucrose 30g / L, agar 6.5g / L, 1 / 2MS medium with a pH of 5.6, under the condition of 25±1°C, 10-12 hours of light per day, after stress culture for 25-30 days, select the surviving buds as the first in vitro Screen salt-tolerant strains, transfer to 1 / 2MS medium with 30g / L sucrose, 6.5g / L agar, PH 5.6, and carry out 25-30 days at 25±1℃, under the condition of 10-12 hours of light per day recovery culture.
Embodiment 3
[0079] Example 3: Secondary in vitro screening of salt-tolerant strains
[0080] Cut off the terminal buds with 3 to 4 leaves of the salt-tolerant strains that have been screened in vitro for the first time after recovery and culture, and transfer them to 1 / 2 of sucrose containing 0.8% NaCl, 30 g / L of sucrose, 6.5 g / L of agar, and PH of 5.6. 2MS medium, under the condition of 25±1°C, 10-12 hours of light per day, after stress culture for 25-30 days, conduct a second in vitro screening: observe the growth status of these buds on the NaCl-containing medium, and eliminate the leaves that turn yellow , wilting or vitrified stems, water-soaked buds, leaving sprouts with dark green leaves and strong stems, added 6-BA 0.2mg / L, KT 0.2mg / L, sucrose 30g / L, Agar 6.5g / L, 1 / 2MS medium with a pH of 5.6, at 25±1°C, under the condition of 10-12 hours of light per day, carry out recovery and proliferation culture according to the strain, and subculture once every 25-30 days. A total of 3 time...
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