Osmunda mildei fertile spore cultivation and reproduction method
A technology for spores and spores of Radix vulgaris is applied in the field of fertile spore culture and reproduction of Radix Radix.
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Embodiment 1
[0021] This embodiment includes the following steps:
[0022] Disinfection treatment of S1 spores:
[0023] From March to May, the sporophytes of Osmanthus fragrans are fully unfolded, and when the sporangia begin to change from dark green to light green, pick off the sporophyll leaves, immediately wash away the floating dust on the surface with clean water, and collect the spores after the water on the surface of the sporophyll leaves is dried or, place the spore leaves in a petri dish covered with sulfuric acid paper, dry them in a desiccator and collect the spore powder. Then put it into a small test tube on the ultra-clean workbench, soak it in sterilized water for 5-10 minutes, centrifuge it with a centrifuge at 3500 rpm, pour off the supernatant, and add 0.1% HgCl 2 Disinfect the solution for 2-6 minutes, rinse with sterilized water for 5-6 times, and finally add an appropriate amount of sterilized water and mix to make a suspension.
[0024] In this step, it is best t...
Embodiment 2
[0048] S1: From March to May, the spore leaves of Osmanthus fruticosa are fully unfolded, and when the sporangia begin to change from dark green to light green, the spore leaves are removed, and the floating dust on the surface is immediately washed away with clean water, and each spore leaflet is removed. Clean the bench with 0.1% HgCl 2 The solution was sterilized for 2-6 minutes, rinsed with sterilized water for 5-6 times, the surface moisture was blotted with sterilized filter paper, and cut into small pieces containing 2-3 sporangia.
[0049] In this step, it is best to sterilize for 5 minutes, and for simple multiplication culture not for the purpose of observing gametophyte development, it is convenient to directly sterilize with sporophylls.
[0050] S2 prothalloid acquisition:
[0051] Inoculate the sporangia fragments sterilized in step S1 on MS basic medium, add hormone 6-benzylpurine 0.5-1.5㎎ / L, naphthaleneacetic acid 0.01-0.1㎎ / L, at a temperature of (25±2)℃, Und...
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Abstract
Description
Claims
Application Information
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