A kind of culture medium for cultivating the mother species of wild reticulata fringe
A culture medium and crimping technology, which is applied in cultivation, application, plant cultivation, etc., can solve the problems of restricting industrial development, teaching and scientific research, and the inability to artificially cultivate wild reticulum crimpingum, and achieve good application prospects and great economic benefits. Value and social benefit, effect of simple preparation method
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Embodiment 1
[0071] The culture medium used in this example for the cultivation of the wild Reticula pleinosa parent species: 20 g of soluble starch, 2 g of peptone, KH 2 PO 4 3.0g, MgSO 4 4.5g, water 1L, pH 4.5.
[0072] 1) Under a sterile environment, cut out about 0.3 cm of the internal tissue block of the fruiting body of the wild Dictyophyllum cringulata and inoculate it in the central part of the PDA slant medium, plug the rubber stopper, mark the name of the strain and the date of inoculation, and place it at 25 After 3-5 days of dark-light cultivation in an incubator at ℃, brown fluffy hyphae germinated from the tissue block. When the mycelium grew to 2-3 cm away from the tissue block, the edge hyphae were picked and transferred to a blank PDA. On the slant medium, when the test tube is overgrown, the purified wild Dictyophyllum cringulae parent species can be obtained;
[0073] 2) Inoculate the purified wild Reticulophyllum cringulata parent species on the PDA plate medium, c...
Embodiment 2
[0077] The culture medium used in this example for the cultivation of the wild Reticula pleurata parent species: 15 g of soluble starch, 2 g of peptone, KH 2 PO 4 1.0g, MgSO 4 0.5g, 1L of water, pH 4.5.
[0078] 1) Under a sterile environment, cut out about 0.3 cm of the internal tissue block of the fruiting body of the wild Dictyophyllum cringulata and inoculate it in the central part of the PDA slant medium, plug the rubber stopper, mark the name of the strain and the date of inoculation, and place it at 25 After 3-5 days of dark-light cultivation in an incubator at ℃, brown fluffy hyphae germinated from the tissue block. When the mycelium grew to 2-3 cm away from the tissue block, the edge hyphae were picked and transferred to a blank PDA. On the slant medium, when the test tube is overgrown, the purified wild Dictyophyllum cringulae parent species can be obtained;
[0079] 2) Inoculate the purified wild Reticulophyllum cringulata parent species on the PDA plate medium...
Embodiment 3
[0083] The medium used in this example for the cultivation of the wild Reticula pleurata parent species: 15 g of soluble starch, 4 g of peptone, KH 2 PO 4 3.0g, MgSO 4 1.5g, water 1L, pH 4.5.
[0084] 1) Under a sterile environment, cut out about 0.3 cm of the internal tissue block of the fruiting body of the wild Dictyophyllum cringulata and inoculate it in the central part of the PDA slant medium, plug the rubber stopper, mark the name of the strain and the date of inoculation, and place it at 25 After 3-5 days of dark-light cultivation in an incubator at ℃, brown fluffy hyphae germinated from the tissue block. When the mycelium grew to 2-3 cm away from the tissue block, the edge hyphae were picked and transferred to a blank PDA. On the slant medium, when the test tube is overgrown, the purified wild Dictyophyllum cringulae parent species can be obtained;
[0085] 2) Inoculate the purified wild Reticulophyllum cringulata parent species on the PDA plate medium, culture i...
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