Method for preparing breeding media and organic fertilizer through edible fungus waste fermentation
A seedling-growing substrate and edible fungus technology, which is applied in the preparation of organic fertilizers, organic fertilizers, and the treatment of bio-organic parts. It can solve the problems of high price and high cost of use, and achieve accelerated respiratory metabolism, efficient acquisition, waste recycling and utilization. The effect of the ecological cycle
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Embodiment 1
[0029] The culture medium and organic fertilizer are prepared by fermenting the culture medium or fungus chaff waste produced during the cultivation of edible fungi as the main raw material. The specific steps are as follows:
[0030] Preparation of high-concentration Bacillus subtilis liquid by submerged liquid fermentation: (1) Enrichment and cultivation of Bacillus subtilis seed liquid at high temperature. The specific steps include: preparing 1000 mL of potato bran juice culture liquid, and equally dividing it into 5 triangles with a specification of 500 mL. The bottle is sealed and bandaged with cotton plugs, double-layer paper, and thread, and is sterilized twice at normal pressure intermittently, that is, sterilized at 100°C for 30 minutes for the first time, cooled to 30°C, kept for 6 hours, and then sterilized at 100°C for 30 minutes ; When the culture solution is cooled to about 50°C, insert Bacillus subtilis, culture temperature is 49°C, shaking speed is 120r / min, cu...
Embodiment 2
[0038] The seedling substrate and organic fertilizer are prepared by fermenting the defective products, broken products and mushroom body debris produced in the edible fungi food processing process as the main raw materials. The specific steps are as follows:
[0039] Preparation of high-concentration Bacillus subtilis and Bacillus natto culture solutions by submerged liquid fermentation: (1) Enrichment and cultivation of Bacillus subtilis seed solutions at high temperature. Put it in a 500mL triangular flask and seal it with cotton plugs, double-layer paper, and thread, and sterilize twice at normal pressure intermittently, that is, sterilize for the first time at 100°C for 30min, cool to 28°C, and keep it for 7h. Sterilize at 100°C for 30 minutes; when the culture solution cools down to about 50°C, add Bacillus subtilis to 5 of the triangular flasks, and add Bacillus natto to the remaining 5 triangular flasks. The culture temperature is 48°C and the shaking speed is 150r / min....
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