Flammulina filiformis strain and identification and breeding method thereof
An identification method, the technology of Flammulina velutipes, applied in the field of edible fungi, can solve the problems of fast and accurate identification of mononuclear, dinuclear and hybrid strains of Flammulina velutipes, and achieve the effects of not easy browning, easy operation, and high biological efficiency
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Embodiment 1
[0050] A strain of Flammulina velutipes, preserved in the General Microbiology Center of China Microbiological Culture Collection Management Committee, address: Institute of Microbiology, Chinese Academy of Sciences, No. 1, No. 1 Beichen West Road, Chaoyang District, Beijing, the preservation number is CGMCCNo.19644, and the preservation date is May 2020 On March 26, it was named Jijin 12; the classification was named: Flammulina filiformis.
[0051] An identification method of Flammulina velutipes strains, one of the two nuclei of the double monohybrid is that the acceptor nucleus is derived from the nucleus of the mononuclear parent, and the other is that the donor nucleus is derived from one of the nuclei of the dinuclear parent. The parents of Jijin 12 include the monokaryotic strain parent and the dikaryotic strain parent. The monokaryotic strain parent is obtained after protoplast monokaryon preparation and regeneration of Flammulina velutipes strain HUANG1, and the dikar...
Embodiment 2
[0073] The breeding method of above-mentioned Flammulina velutipes bacterial strain, comprises the steps:
[0074] Inoculate the mycelium of Flammulina velutipes strain HUANG1 in an Erlenmeyer flask filled with liquid medium, culture it statically at 25°C for 8 days, and shake the flask by hand every 24 hours. Mycelia, with a mass concentration of 2% lysozyme enzyme solution (purchased from Guangdong Provincial Institute of Microbiology), enzymolysis at 30 ° C for 4 hours, filtered off broken mycelia, washed 3 times with 0.6M sucrose solution, and purified Dilute the protoplast suspension with 0.6M sucrose solution to a concentration of 300 cells / ml, draw 0.2ml and spread it on the regeneration medium, cultivate it at 25°C for 8 days, pick a single colony and store it on the slant of the test tube, and store it on the slant of the test tube Cultivate at 25°C for 4 days, take mycelium slices, and observe under a microscope whether there is a lock junction. If there is no lock j...
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