Preparation method of tricholoma matsutake mycelium fermented vinegar beverage
A technology of mycelium fermentation and vinegar beverage, which is applied in the preparation of vinegar, etc., can solve the problems of long growth cycle, high cost, and difficulty in manual acquisition, and achieve the effect of short cultivation time and reduced raw material cost
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specific Embodiment approach 1
[0043] Specific implementation mode one: as Figure 26 Shown, a kind of preparation method of matsutake mycelium fermented type vinegar beverage comprises the following steps:
[0044] Step 1: Activate matsutake thalline, inoculate the activated matsutake fungus on the liquid medium with an inoculation amount of 10% volume ratio for cultivation, homogenate and filter the culture solution containing matsutake mycelium after cultivation, and use sucrose adjusting the sugar content to 13.0% to obtain the adjusted matsutake culture solution;
[0045] Step 2: inserting yeast and acetic acid bacteria slant-preserved strains into yeast culture medium and acetic acid bacteria culture medium respectively, and carrying out expanded cultivation;
[0046] Step 3: inserting the saccharomycetes after step 2 expanded culture into the matsutake culture solution obtained in step 1 to carry out alcohol fermentation single factor test;
[0047] Step 4: Carry out the alcohol fermentation optimi...
specific Embodiment approach 2
[0051] Specific embodiment two: the difference between this embodiment and specific embodiment one is: the specific process of matsutake thalline activation in the step one is:
[0052] Insert the preserved strains into the matsutake slant culture medium with an inoculation needle, and cultivate at 23-25°C for 7-8 days. The matsutake slant culture medium is 2g of glucose, 0.3g of peptone, KH 2 PO 4 0.1g, MgSO 4 0.05g and 2g of agar were added to the potato juice and the volume was adjusted to 100ml.
[0053] Other steps and parameters are the same as those in Embodiment 1.
specific Embodiment approach 3
[0054] Specific embodiment 3: The difference between this embodiment and specific embodiment 1 or 2 is that: in the step 1, the culture temperature for inoculating on the liquid medium for cultivation is 20-22°C, and the rotating speed of the shaker is 150-160r / min. Cultured for 28-30 days, the liquid medium is: 3g of sucrose, 2g of maltose, 0.25g of yeast powder, 0.25g of wheat bran, KH 2 PO 4 0.025g and MgSO 4 ·7H 2 O 0.015g was added to water and the volume was adjusted to 100ml.
[0055] Other steps and parameters are the same as those in Embodiment 1 or Embodiment 2.
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