Method for in vitro culture of Taishan Polygonatum sibiricum ovules
A culturing method and ovule technology are applied in the field of culturing ovules of Polygonatum taishani in vitro, which can solve the problems of non-germination and low harvest rate of mature seeds, and achieve the effects of reducing operation procedures, improving seedling reproduction efficiency and shortening reproduction process.
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Embodiment approach 1
[0035] Implementation Mode 1: Direct Stripping
[0036] The vigorous Taishan Polygonatum field seedlings were selected as the test plants, and the young seeds free from diseases and insect pests at the 3-6 round leaves of the plant from the ground up 14-20 days after fertilization were used as explant materials. Young seeds are green and spherical, preferably 0.3-0.5 cm in length and width.
[0037]Firstly, the residual corolla and sepals coated on the surface of the young seeds are peeled off, rinsed with running water, and then aseptically sterilized.
[0038] First disinfect with 70% alcohol for 15-30s, then disinfect with 0.1% mercuric chloride solution for 7-10min, rinse with sterile water for 3-5 times, and then blot the surface dry for later use.
[0039] The aseptic ovules were obtained by direct stripping. The specific treatment method for the sterilized juvenile seed explants is as follows: starting from the abdominal suture of the ovary, cut the ovary wall to expo...
Embodiment approach 2
[0046] Embodiment 2: Transecting the ovary wall
[0047] The vigorously growing Taishan Polygonatum field seedlings were selected as the test plants, and the young seeds free from diseases and insect pests at the 3-6 wheel-shaped leaves of the plant from the ground up 14-20 days after fertilization were used as explant materials. The juvenile seeds are green and spherical, preferably 0.3-0.5 cm in length and width.
[0048] Firstly, the residual corolla and sepals coated on the surface of the young seeds are peeled off, rinsed with running water, and then aseptically sterilized.
[0049] First disinfect with 70% alcohol for 15-30s, then disinfect with 0.1% mercuric chloride solution for 7-10min, rinse with sterile water for 3-5 times, and then blot the surface dry for later use.
[0050] Aseptic ovules were obtained by transecting the ovary wall. The specific treatment method for the sterilized juvenile seed explants is as follows: cut off about 1 / 3-1 / 2 of the ovary wall by ...
Embodiment approach 3
[0054] Embodiment 3: Only part of the epidermis of the ovary wall is removed but the complete ovary is preserved
[0055] The vigorously growing Taishan Polygonatum field seedlings were selected as the test plants, and the young seeds free from diseases and insect pests at the 3-6 wheel-shaped leaves of the plant from the ground up 14-20 days after fertilization were used as explant materials. The juvenile seeds are green and spherical, preferably 0.3-0.5 cm in length and width. The culture conditions at this stage are as follows: first culture in the dark for 7-14 days, then transfer to normal light culture for 12 hours / day, and the temperature is about 25°C;
[0056] Firstly, the residual corolla and sepals coated on the surface of the young seeds are peeled off, rinsed with running water, and then aseptically sterilized. First disinfect with 70% alcohol for 15-30s, then disinfect with 0.1% mercuric chloride solution for 7-10min, rinse with sterile water for 3-5 times, and ...
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