Seedling raising method for mutagenizing calluses of bamboo used for fibers through internal and external irradiation
A technology of callus and fiber, which is applied in the field of raising seedlings of bamboo callus for mutagenic fiber by internal and external irradiation, can solve the problems of single variety type, death, and uncertainty of bamboo plant flowering, and achieve a wide range of breeding materials, The effect of fast offspring traits and short breeding time
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Embodiment 1
[0030] Select the callus induced by the branch stem buds of Cizhu with cellulose content of 54% and lignin content of 23%. internal mutagen Na 131 1, be prepared into the mutagen solution of 15GBq. Inject 20 μL of 15 GBq mutagen solution into the callus of Cizhu with a size of about 0.05-1.0 cm with a stainless steel continuous syringe. The callus injected with mutagen was placed in 15GBq of mutagen solution and shaken for 120min at a shaking speed of 90rpm. Inoculate the mutagenized callus on the shoot induction medium, grow shoots after 25 days, and obtain complete regenerated plants after 15 days after in vitro induction of roots. Mutant plants were obtained by screening with ISSR molecular marker technology, and 360 days after transplanting, the new germplasm of Cizhu with excellent properties was screened.
Embodiment 2
[0032] The callus induced by branch stem buds of Arthia lanceolata was selected as fiber with 52% cellulose content and 22% lignin content. internal mutagen Na 131 1, be prepared into the mutagen solution of 25GBq. Inject 40 μL of 25 GBq mutagen solution into the callus of Cizhu lanceolata with a size of about 0.05-1.0 cm with a stainless steel continuous syringe. The callus injected with mutagen was placed in 25GBq of mutagen solution and shaken for 90min at a shaking speed of 90rpm. Inoculate the mutagenized callus on the shoot induction medium, grow shoots after 20 days, and obtain complete regenerated plants after 25 days after in vitro induction of roots. Mutant plants were obtained by screening with ISSR molecular marker technology, and 360 days after transplanting, the new germplasm of Arthia lanceolata for fiber with excellent properties was screened.
Embodiment 3
[0034] The callus induced by the branch stem buds of green bamboo was selected to select fibers with 42% cellulose content and 27% lignin content. internal mutagen Na 131 I, the mutagen solution that is mixed with 10GBq. Inject 50 μL of 10 GBq of the mutagen solution into the callus with a size of about 0.05-1.0 cm using a stainless steel continuous syringe. The callus injected with mutagen was placed in 10GBq of mutagen solution and shaken for 180min at a shaking speed of 90rpm. Inoculate the mutagenized callus on the shoot induction medium, grow shoots after 30 days, and obtain complete regenerated plants after 15 days after in vitro induction of roots. Mutant plants were obtained by screening with ISSR molecular marker technology, and 360 days after transplanting, new germplasm of green bamboo for fiber with excellent properties was screened.
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