A kind of Flammulina velutipes strain and its identification and breeding method
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 bright colors, high biological efficiency, and good palatability
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Embodiment 1
[0050] A strain of Flammulina velutipes, preserved in the General Microbiology Center of China Microbial Culture Collection Management Committee, address: Institute of Microbiology, Chinese Academy of Sciences, No. 3, No. 1 Beichen West Road, Chaoyang District, Beijing, preservation number: CGMCCNo.19644, preservation date: May 2020 On March 26, it was named Jijin 12; classification name: Flammulinafiliformis.
[0051] A method for identifying Flammulina velutipes strains, the two cell nuclei of the double monohybrid are one of the acceptor nucleus derived from the mononuclear parent, and the other one of the donor nucleus derived from the dinuclear parent. The parents of Jijin 12 include monokaryotic strain parents and dikaryotic strain parents. The monokaryotic strain parent is obtained by the preparation and regeneration of protoplast monokaryon of Flammulina velutipes strain HUANG1, and the dikaryotic parent is the fruit body of wild Flammulina velutipes strain JHH by tissu...
Embodiment 2
[0073] The breeding method of above-mentioned Flammulina velutipes strain, comprises the steps:
[0074] Take the mycelium of the yellow cultivated Flammulina velutipes strain HUANG1 and inoculate it in a conical flask filled with a liquid medium, culture at 25°C for 8 days, shake the conical flask by hand every 24h, and collect the conical flasks in the liquid medium under aseptic conditions. Mycelium, with 2% lysozyme enzyme solution (purchased from Guangdong Institute of Microbiology), enzymatically hydrolyzed at 30 ° C for 4 hours, filtered off the broken mycelium, washed 3 times with 0.6M sucrose solution, and purified The protoplast suspension was diluted with 0.6M sucrose solution to a concentration of 300 / ml, and 0.2ml was drawn and spread on the regeneration medium, cultured at 25°C for 8 days, and a single colony was picked and stored on the slant of the test tube. Cultivate at 25°C for 4 days, take the mycelium slices, and observe under the microscope whether there ...
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