Maka seedling reproducing method
A technology for seedlings and maca, which is applied in the field of plant bioengineering and biology to achieve the effects of excellent variety characteristics, low cost and good economic benefits
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Embodiment 1
[0015] Select the leaves of living plants with good growth, wash them repeatedly with tap water, and treat them with 70% ethanol for 20 seconds or 5% hydrogen peroxide for 3 minutes in an ultra-clean environment. After repeated washing with sterile water, use 8% hypochlorite Salt solution for 10 minutes of disinfection. After repeated rinsing with sterile water, cut into small sections of 1 cm, used as explants for inoculation culture, callus induction, differentiation of adventitious buds and rooting culture, the culture conditions were light intensity 1500LX, daily light time For 16 hours, the culture temperature was 22±2 degrees. First carry out callus induction: adopt MS improved medium (keep the trace element in MS medium, organic element remains unchanged, the content of macroelement is KNO 3 1250mg / L, NH 4 NO 3 1650mg / L, KH 2 PO 4 370mg / L, MgSO 4 ·7H 2 O 370mg / L, CaCl 2 440mg / L), add 0.7% agar, 6BA concentration is 0.5mg / L, NAA concentration is 0.5mg / L, can i...
Embodiment 2
[0017] Select the stems of living plants with good growth, wash them repeatedly with tap water, and then treat them with 70% ethanol for 10 seconds or 5% hydrogen peroxide for 5 minutes in an ultra-clean environment. After repeated washing with sterile water, use 10% hydrogen peroxide. The sodium hypochlorite solution was disinfected for 8 minutes. After repeated rinsing with sterile water, cut into small sections of 1 cm and use them as explants for inoculation and culture for callus induction and differentiation of adventitious buds and rooting culture. The time is 16 hours, and the culture temperature is 22±2 degrees. First carry out callus induction: adopt MS improved medium (keep the trace element in MS medium, organic element remains unchanged, the content of macroelement is KNO 3 2500mg / L, NH 4 NO 3 150mg / L, KH 2 PO 4 150mg / L, MgSO 4 ·7H 2 O 200mg / L, CaCl 2 110mg / L), add 1.0% agar, 6BA concentration is 0.5mg / L, NAA concentration is 0.5mg / L, just can induce th...
Embodiment 3
[0019] The plump maca seeds that will be selected are washed with tap water, and then 10mg / L of gibberellin (GA 3 ) soaking treatment, then sterilize, and the sterilized method is the same as in Example 2, insert the sterilized seeds into the MS culture medium without exogenous hormones, add 0.9% agar or 1.0% carrageenan or directly add inert solids in the liquid medium Particles such as glass beads, perlite, vermiculite. After 3 weeks, when the seedlings grow to a height of 4-5 cm, a sterile seedling is obtained. Select aseptic seedlings with good growth, cut the leaves as explants, and cut them into 1cm segments for callus induction, adventitious bud differentiation and rooting culture. The culture conditions are light intensity of 1500LX, daily light For 16 hours, the culture temperature was 24±2 degrees. First carry out callus induction: adopt MS improved medium (keep the trace element in MS medium, organic element remains unchanged, the content of macroelement is KNO 3...
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