Method for identifying hericium erinaceus strain king by utilizing molecule marker technology
A technology of molecular markers and technical identification, applied in the direction of biochemical equipment and methods, microbiological determination/inspection, etc., can solve the difficulties in standardizing production and product quality standards, the same name or different names of different species of Hericium erinaceus, damage Issues such as the interests of breeders and producers, to achieve the effect of short detection time, high accuracy and reduced deviation
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Embodiment 1
[0025] Embodiment 1: A kind of method utilizing molecular marker technology to identify Hericium erinaceus strain Monkey King
[0026] A method utilizing molecular marker technology to identify Hericium erinaceus strain Monkey King, comprising the following steps:
[0027] 1. Mycelia culture and collection.
[0028] (1) If the storage time of the test Hericium erinaceus strain is less than 6 months, the mycelia culture shall be carried out as follows:
[0029] 1. Use an inoculation rake to crush the PDA medium containing Hericium erinaceus mycelia, and transfer it to a 250 ml Erlenmeyer flask containing 100 ml PDA liquid medium;
[0030] 2. Place on a shaker at 25°C with a rotation speed of 90-130 r / min and incubate for 7-10 days;
[0031] 3. Filter the cultured mycelia with gauze, rinse with distilled water, and dry with filter paper;
[0032] 4. Weigh 0.5-1.3 g of mycelium, wrap it with filter paper, and store it at -20°C for later use.
[0033] (2) If the Hericium erina...
Embodiment 2
[0062] Embodiment 2: A kind of method utilizing molecular marker technology to identify Hericium erinaceus strain Monkey King
[0063] A method utilizing molecular marker technology to identify Hericium erinaceus strain Monkey King, comprising the following steps:
[0064] One, mycelia culture and collection, the specific method is the same as the step one of embodiment 1;
[0065] Two, the extraction of genomic DNA, described genomic DNA can be extracted from the mycelium of bacterial strain or fruit body; Concrete method is identical with the step 2 of embodiment 1;
[0066] 3. Establishment of the detection of SCAR-PCR molecular markers, wherein the SCAR-PCR amplification system is the same as the amplification system in Step 3 of Example 1; the SCAR-PCR reaction conditions are: 94° C. for 1 min;
[0067] 94°C 45second, 67°C 45second, 72°C 1min, 30 cycles; 72°C 5min.
[0068] The special detection primer Monkey King F2 / R2 uses PCR technology to obtain the specific DNA fra...
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