Seed production method of bamboo callus for internal irradiation and chemical mutagenesis fibers
A callus and chemical mutagenesis technology, applied in the field of plant radiation mutagenesis breeding, can solve the problem of not establishing a new set of bamboo germplasm for fiber, immature bamboo genetic transformation system, uncertainty of flowering of bamboo plants, etc. problem, to achieve the effect of fast offspring traits, fast stability and short breeding time
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Embodiment 1
[0031] A callus with 54% cellulose content and 23% lignin content was selected to induce callus with the branches and shoots of Ci bamboo. Select internal radiation mutagens Na 131 I. Prepare a mutagen solution of 15GBq. The chemical mutagen EI (ethylene imine) was selected and prepared into a 0.6% mutagens solution. A stainless steel continuous syringe was used to inject 20 μL of 15GBq of internal radiation mutagens solution into callus with a size of about 0.05-1.0 cm. The callus injected with internal radiation mutagens was placed in a 0.6% ethyleneimine mutagens solution and shaken for 120 minutes at a shaking speed of 90 rpm. The mutagenized callus was inoculated on the bud induction medium, and buds were grown after 20 days. After the in vitro root induction, complete regenerated plants were obtained after 18 days. The mutant plants were screened by ISSR molecular marker technology, and after 360 days of transplantation, new germplasm for fiber use with excellent proper...
Embodiment 2
[0033] A callus with a cellulose content of 52% and a lignin content of 22% was selected from the callus induced by the branching stem buds of Azalea liangshanensis. Select internal radiation mutagens Na 131 I. Prepare 25GBq mutagen solution. Select the chemical mutagens EI (ethylene imine) and prepare a 1.2% mutagens solution. A stainless steel continuous syringe was used to inject 30 μL of 25GBq internal radiation mutagens solution into callus with a size of about 0.05-1.0 cm. The callus injected with internal radiation mutagens was placed in 1.2% ethyleneimine mutagens solution and shaken for 90 minutes at a shaking speed of 90 rpm. The mutagenized callus was inoculated on the bud induction medium, and buds were grown after 26 days. After in vitro root induction, complete regenerated plants were obtained after 30 days. The mutant plants were screened by ISSR molecular marker technology. After 360 days of transplanting, new germplasm of Liangshan Cizhu for fiber was screene...
Embodiment 3
[0035] Select the callus induced by the branches and shoots of green bamboo fiber with 42% cellulose content and 27% lignin content. Select internal radiation mutagens Na 131 I. Prepare a mutagen solution of 10GBq. Select the chemical mutagens EI (ethylene imine) and prepare a 1.5% mutagens solution. Use a stainless steel continuous syringe to inject 50 μL of 10 GBq of internal radiation mutagens solution into callus with a size of about 0.05 to 1.0 cm. Place the callus filled with internal radiation mutagens in a 1.5% ethyleneimine mutagens solution and shake for 70 minutes at a shaking speed of 90 rpm. The mutagenized callus was inoculated on the bud induction medium, and buds grew after 27 days. After the roots were induced in vitro, complete regenerated plants were obtained after 23 days. The mutant plants were screened by ISSR molecular marker technology. After 360 days of transplantation, new germplasms of green bamboo for fiber were screened.
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