An optimized method for efficiently and rapidly constructing a library of homogeneous mutants with high saturation and high resistance in stepgrass
An optimization method and a step-grass technology, applied in the fields of botanical equipment and methods, horticultural methods, plant regeneration, etc., can solve the problem of difficult to quickly obtain genetically stable mutation-rich and directional mutation homogeneous mutants, difficult to saturate Targeted homogeneous mutant library and other issues, to achieve the effect of low cost, uniform distribution, and increased capacity
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Embodiment 1
[0042] Example 1 illustrates the optimization method for the construction of a library of homogeneous mutants with high efficiency, rapid saturation and high resistance to C. argentina as an example. The steps are:
[0043] 1) High-frequency somatic embryo explant material preparation and early stage somatic embryo explant culture: select healthy and pest-free plants of A. figure 1 : Thin-leafed Grass; Dwarf Grass and Black Grass), peel off the old leaves, take its young stem base with 3-4 young leaves, put it into a sterile medium for cultivation after aseptic disinfection (1 / 2MS+2.0mg / L BA+0.5mg / L NAA+sucrose 20g / L+0.7% agar) 50-60d, subculture once in the middle, tissue culture into test-tube plantlets, take 0.5- 1.0cm size explants were placed in somatic embryogenesis induction medium (MS+BA(0.2mg / L)+NAA(0.5mg / L)+2.4D(0.5mg / L)+sucrose 30g / L+3.5g / L phytagel) for 50-56 days, subculture once in the middle, and transfer the resulting primary embryoid bodies to high-frequenc...
Embodiment 2
[0059] Example 2 illustrates the optimization method for the construction of a library of homogeneous mutants with high efficiency, rapid saturation and high resistance to C. nigella in C. nigella as an example. The steps are:
[0060] 1) Preparation of high-frequency somatic embryo explant material and cultivation of early somatic embryo explant: select healthy and pest-free plants of Nigella nigra, peel off old leaves, take its young stem base and bring 3-4 Young leaves, aseptically sterilized, placed in sterile medium for culture (1 / 2MS+2.0mg / L BA+0.5mg / L NAA+sucrose 20g / L+0.7% agar) for 50-60d, subcultured once in the middle, group Cultivate test-tube plantlets, get its test-tube plantlet leaves, stem base 0.5-1.0cm size explants, put on somatic embryogenesis induction medium (MS+BA(0.2mg / L)+NAA(0.5mg / L)+2.4 D (0.5mg / L)+sucrose 30g / L+3.5g / L phytagel) was cultured for 50-56d, subcultured once in the middle, and the primary embryoid bodies produced were transferred to high-...
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