Method for cultivating octoploid lowland type switchgrass
An octoploid and willow branch technology, applied in the field of plant breeding, can solve the problems of limited germplasm resources and single planting varieties, and achieve the effects of fewer chimera plants, mature methods, and stable doubling effects
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Embodiment 1
[0036] Taking the tetraploid lowland switchgrass variety Alamo as the research object, at the booting stage, cut the immature young ears of switchgrass with bracts that grew robustly, stripped the outer bracts and leaf sheaths, and cut the young ears with inner bracts into 1.8 -2.2 cm segments to obtain young ear segments containing inner bracts. On the ultra-clean workbench, first disinfect the surface with 75% ethanol by volume for 30 seconds, rinse with sterile distilled water twice, then sterilize with 20% NaClO by volume for 10 minutes, and finally use sterile distilled water Wash 3-4 times, place on sterilized filter paper, and blot the surface moisture.
[0037] 1): Cut the sterilized young ear section containing the inner bract lengthwise into two halves, and then inoculate it in induction medium (MS basic medium + 3% maltose + 5mg / L2, 4-D + 1.2mg / L6 -BA+0.8% plant gel, pH value 5.8), induce callus tissue under dark conditions at 25±2°C, subculture after 10 days, subc...
Embodiment 2
[0048] Taking the tetraploid lowland switchgrass variety Kanlow as the research object, at the booting stage, cut the immature young ears of switchgrass with bracts growing vigorously, stripped the outer bracts and leaf sheaths, and cut the young ears with inner bracts into 1.8 -2.2 cm segments to obtain young ear segments containing inner bracts. On the ultra-clean workbench, first disinfect the surface with 75% ethanol by volume for 30 seconds, rinse with sterile distilled water twice, then sterilize with 20% NaClO by volume for 10 minutes, and finally use sterile distilled water Wash 3-4 times, place on sterilized filter paper, and blot the surface moisture.
[0049] 1): Cut the sterilized young ear section containing the inner bract lengthwise into two halves, and then inoculate it in induction medium (MS basic medium + 3% maltose + 5mg / L2, 4-D + 1.2mg / L6 -BA+0.8% plant gel, pH value 5.8), induce callus tissue under dark conditions at 25±2°C, subculture after 10 days, sub...
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