Fast teething and reproduction method for Mafeng tree
A Jatropha curcas, fast technology, applied in horticultural methods, botanical equipment and methods, plant regeneration, etc., can solve the problems of loss of good traits, high variation rate of differentiated seedlings, Jatropha curcas is susceptible to seasonal and geographical restrictions, etc. Achieve the effects of avoiding the maintenance of excellent traits, fast propagation speed and high number of buds
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Embodiment 1~6、 comparative example 1
[0024] This group of embodiment and comparative example all adopt the Jatropha curcas stem tip of natural growth to carry out rapid propagation.
[0025] Sterilization process is carried out according to each embodiment and comparative example inoculation quantity, intercepts the Jatropha curcas stem tip 1~2cm of natural growth respectively, puts into 70% alcohol and shakes 1min, discards alcohol, then uses 0.1% HgCl 2 The solution was sterilized for 7 minutes, and the HgCl was discarded 2 , and then rinsed 5 times with sterile water to thoroughly wash away residual HgCl 2 .
[0026] Preparation of rapid propagation medium In MS medium numbered from (1) to (9), add cytokinin 6-benzyladenine (BA), auxin indole and butyric acid (IBA) and silver nitrate, and adjust its pH to 5.8.
[0027] Rapid Propagation Absorb the water on the surface of the shoot tip after sterilization, cut off the excess part, keep only the tender part of the tip, and then transfer it into the rapid prop...
Embodiment 9~17
[0032] The examples of this group all adopt the aseptic vaccine that is cultivated by hormone stimulation to carry out rapid propagation.
[0033] Sterilize the quantity inoculated according to each embodiment, peel off the seed coat of Jatropha curcas seeds, take out the embryo therein, put into 70% alcohol and shake for 1min, discard the alcohol, then use 0.1% HgCl 2 The solution was sterilized for 7 minutes, and the HgCl was discarded 2 , and then rinsed 3 times with sterile water to thoroughly wash away residual HgCl 2 , add sterile water to soak for 48 hours, then pour out the sterile water. Operate again according to the above sterilization process.
[0034] Cultivate aseptic seedlings to absorb the water on the surface of the seed kernel after sterilization, cut the seed kernel (endosperm) along the longitudinal axis with a blade, and peel off two white cotyledons (the bases of the two cotyledons contain the seed embryo), and connect the cotyledons together. Embryos ...
Embodiment 18
[0041] The germs of the sterilized seedlings that germinated in the sterile seedlings that were sterilized and cultivated in the procedures described in Examples 9 to 17 were excised, and inoculated with 20 inoculations made of MS+2.0mg / L zeatin+0.05mg / L indole Acetic acid (IAA)+5mg / L AgNO 3 In the composed rapid propagation medium, the pH value of the medium is 4.8, and after 25 days of culture under the conditions of culture temperature 30°C, light intensity 2000lx, and light time 8h / d, the average number of axillary buds induced is 2.70.
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