Drying method of isaria cicadae sporocarps
A drying method, the technology of cicadae, which is applied in food drying, food science, and preservation of fruits/vegetables through dehydration, etc., can solve the problems that the production process and product stability cannot be guaranteed, the active ingredients change significantly, and there are many limiting factors. Achieve the effect of improving appearance color, retaining more easily, preventing conversion and loss
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Embodiment 1
[0023] The artificial cultivation of embodiment 1 cicada
[0024] 1. Training process
[0025] Incline cultivation → liquid cultivation (shake flask cultivation → seed tank cultivation → fermenter cultivation) → solid cultivation → harvesting;
[0026] 2. Medium
[0027] Incline medium: PSA medium (potato boiled juice 200g, white sugar 20g, agar powder 20g, the remaining water to make up 1L);
[0028] Liquid medium: YSPS medium (5g of yeast extract, 10g of soybean protein isolate, 35g of white sugar, and the remaining water to make up 1L);
[0029] Solid medium: mix wheat and water in a ratio of 1:1.5;
[0030] The medium should be sterilized to ensure sterility;
[0031] 3. Culture conditions
[0032] Slope culture stage: temperature 22°C, time: about 7 days;
[0033] Shake flask culture stage: speed: 150r / min, temperature: 25±1°C, time: culture 55-60h;
[0034] Seed tank culture (fermentation tank) stage: speed: 150r / min, 1.5vvm, temperature: 25°C, time: culture 24-36...
Embodiment 2
[0036] The artificial cultivation of embodiment 2 cicadae
[0037] The culture process and culture conditions are the same as in Example 1, the difference being that the culture medium is different:
[0038] The slant medium is: SDAY medium (yeast extract powder 10.0g, glucose 40.0g, peptone 10.0g, agar 20.0g, pH 6.0±0.1);
[0039] Liquid medium: Richard medium (KNO3 10g, KH2PO45g, MgSO4 2.5g, sucrose 50g, FeCl3 0.02g, distilled water 1L);
[0040] Solid medium: Mix rice and water in a ratio of 1:1.3.
Embodiment 3
[0041] The artificial cultivation of embodiment 3 cicadae
[0042] The culture process and culture conditions are the same as in Example 1, the difference being that the culture medium is different:
[0043] The slant medium is: MPA medium (maltose 40g, peptone 10g, agar 20g, distilled water 1L);
[0044] The liquid medium is: PGY medium (peptone 5g, glucose 10g, yeast extract 10g, distilled water 1L);
[0045] Solid medium: Mix millet and water in a ratio of 1:1.3.
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