Method for preparing precocious white needle mushroom strain
A technology of white Flammulina velutipes and yellow golden needles, applied in botany equipment and methods, horticulture, applications, etc., can solve the problems of long cultivation period of white Flammulina velutipes, deepening of the base of the stipe, early fruiting, etc.
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Embodiment 1
[0029] Example 1 , a kind of creation method of precocious white Flammulina velutipes bacterial strain, comprises the following steps:
[0030] (1) Monokaryon isolation and identification, the operation method is as follows:
[0031] a, spore collection, take out the mature fruiting body cap of Flammulina velutipes strain "Golden Silk", place it on sterile paper, and place it for 20 hours until spore prints appear on the sterile paper.
[0032] b. Spore germination culture, remove the spore print on the sterile paper and put it in sterile water to make a spore liquid, then dilute the spore liquid to 80 / ml with sterile water, take 1 ml of the spore liquid and coat the medium plate Above, the culture medium is yeast powder glucose agar medium, cultivated at 25°C for 5 days, until the spores germinate into white colonies, take a single white colony and transfer to yeast powder glucose medium, and cultivate at 25°C.
[0033] c. Monokaryon identification: take the mycelium and pl...
Embodiment 2
[0050] Example 2, A kind of creation method of precocious white Flammulina velutipes bacterial strain, comprises the following steps:
[0051] (1) Monokaryon isolation and identification, the operation method is as follows:
[0052] a. Spore collection, take out the mature fruiting body cap of Flammulina velutipes strain "Golden Silk", place it on sterile paper, and place it for 24 hours until spore prints appear on the sterile paper.
[0053] b. Spore germination culture, remove the spore print on the sterile paper and put it into sterile water to make a spore liquid, then dilute the spore liquid to 100 / ml with sterile water, and take 1 ml of the spore liquid to coat the medium plate Above, the culture medium is yeast powder glucose agar medium, cultured at 28°C for 4 days, until the spores germinate into white colonies, and a single white colony was transferred to yeast powder glucose agar medium, and cultured at 28°C.
[0054] c. Monokaryon identification: take the mycel...
Embodiment 3
[0071] Example 3 , a kind of creation method of precocious white Flammulina velutipes bacterial strain, comprises the following steps:
[0072] (1) Monokaryon isolation and identification, the operation method is as follows:
[0073] a. Spore collection, take out the mature fruiting body cap of Flammulina velutipes strain "Golden Silk", place it on sterile paper, and place it for 12 hours until spore prints appear on the sterile paper.
[0074]b. Spore germination culture, remove the spore print on the sterile paper and put it into sterile water to make a spore liquid, then dilute the spore liquid to 50 / ml with sterile water, and take 1 ml of the spore liquid to coat the medium plate Above, the culture medium is yeast powder glucose agar medium, cultivated at 20°C for 6 days, until the spores germinate into white colonies, and transfer a single white colony to yeast powder glucose agar medium, and culture at 20°C.
[0075] c. Monokaryon identification: take the mycelium and...
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