Method for obtaining sesame wild species and cultivar distant hybrid progeny through adopting immature embryo saving technology
A technology of young embryo rescue and distant hybridization, applied in the fields of botanical equipment and methods, horticultural methods, applications, etc., can solve problems such as inability to obtain hybrid plants, hybrid unfruitful, hybrid embryo abortion, etc., and achieve good disease resistance and resistance. Inverse traits, overcoming incompatibility, effects of improved germplasm
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Embodiment 1
[0040] A method for obtaining distant hybrid offspring of wild sesame and cultivated sesame by using immature embryo rescue technology, comprising the following steps: (1) parental material preparation: the female parent selects a comprehensive trait comparison of 40-50 days from sowing to flowering. A good cultivar "Zhongzhi 14"; the male parent uses the wild species "Yezhi 5" (S.radiatum, 2n=64) as material, and selects disease-free and plump seeds for planting;
[0041] (2) Distant hybridization: when both parents are in bloom, remove the white corolla and stamens of the female parent, and list them; use the male parent to pollinate, record the number of hybrid flowers, and the number of pollinated capsules;
[0042] (3) Stripping of ovules: respectively select young capsules at the developmental stage of 12d to 18d after cross-pollination, rinse the surface with clear water, disinfect the surface of the young capsules with 75% alcohol for 30 seconds under the ultra-clean wo...
Embodiment 2
[0057]The method described in this example to use the immature embryo rescue technology to obtain the distant hybrid offspring of wild sesame and cultivated sesame is basically the same as that of Example 1, the difference is that: (1) the immature embryo induction medium is: based on MS Add 0.5mg / L gibberellin, 1mg / L6-benzylaminoadenine, 30g / L sucrose and 8g / L agar in the medium, and the pH value of the medium is 5.8; the differentiation medium is: basic culture in MS Add 0.6mg / LIBA, 0.8mg / LAgNO3, 30g / L sucrose and 8g / L agar in the medium, and the pH value of the culture medium is 5.8; Both: temperature 28~30°C, photoperiod 8h / d, light intensity 2000lux; (3) The rooting medium is: add 0.5mg / LNAA, 30g / L sucrose and 8g / L agar to MS basic medium , the pH value of the medium is 5.8; the proliferation medium is: add, 3mg / L6-BA, 2mg / LIAA, 30g / L sucrose and 8g / L agar in MS basic medium, the pH value of the medium is 5.8.
[0058] The hybrid F obtained by crossing this embodiment ...
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