Method for direct regeneration of adventitious bud from Jatropha curcas petiole explant
A technology of explants and tree petioles, applied in the field of plant biology, can solve the problems of low regeneration rate, poor quality of regenerated buds, long regeneration cycle, etc., achieve the effect of simple method, reduce negative impact, and shorten the cultivation cycle
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Embodiment 1
[0030] S1. Preparation of Vessels for Short-Term Cytokinin Solution Treatment of Explants
[0031] Select a petri dish with a diameter of 9 cm, place it in a high-pressure steam sterilizer, and sterilize it at 121 °C and 0.1 MPa for 20 minutes.
[0032] S2. Preparation of phenylthiadiazolyl urea (TDZ) treatment solution.
[0033] Accurately weigh a certain amount of TDZ powder, fully dissolve it with 1 N NaOH solution, and then dilute it with deionized water to prepare 0, 0.5, 1, 2, 3, 6, 12 mg / L TDZ treatment solutions. Use 1 N HCl solution to adjust the pH of the TDZ treatment solution to 5.8-6.0; filter and sterilize the prepared TDZ treatment solution with a 0.22 micron water filter before use.
[0034] S3. Surface sterilization of Jatropha curcas petiole and acquisition of petiole explant
[0035] Use scissors to cut a number of petioles of similar length near the top of the stem from an adult Jatropha curcas tree. After rinsing the petioles with tap water for 3...
Embodiment 2
[0051] S1. Preparation of the container for short-term cytokinin solution treatment of explants: same as in Example 1.
[0052] S2. Prepare a 3 mg / L phenylthiadiazolyl urea (TDZ) solution, and the specific preparation method is the same as that in Example 1.
[0053] S3. Surface sterilization of Jatropha curcas petioles and acquisition of petiole explants: the specific method is the same as in Example 1.
[0054] S4. Cytokinin (TDZ) solution treatment of Jatropha curcas petiole explants
[0055] In the ultra-clean workbench, place the cut petiole explants in the sterilized petri dishes prepared in the above step S1, and pour the 3 mg / L of the above-mentioned step S2 into each of the petri dishes. TDZ solution until the petiole explants were submerged, covered with the lid of the petri dish, and left to stand for 0, 5, 10, 20, 40, and 80 minutes respectively (the soaking treatment time of the control group was 0 minutes means that the petiole explants were not ...
Embodiment 3
[0064] S1. Preparation of the container for short-term cytokinin solution treatment of explants: same as in Example 1.
[0065] S2. Prepare a 3 mg / L phenylthiadiazolyl urea (TDZ) solution, and the specific preparation method is the same as in Example 1.
[0066] S3. Surface sterilization of Jatropha curcas petioles and acquisition of petiole explants: the specific method is the same as in Example 1.
[0067] S4. Cytokinin (TDZ) solution treatment of Jatropha curcas petiole explants
[0068] In the ultra-clean workbench, place the cut petiole explants in the sterilized petri dishes prepared in the above step S1, and pour the 3 mg / L TDZ prepared in the above step S2 into each of the petri dishes. Solution until the petiole explants are immersed in the petiole explants, cover the petri dish, and after standing for 5 minutes, pour off the TDZ solution, keep the petiole, take out all the petiole explants from the petri dish with sterilized tweezers, and place them ...
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