Microbial fermentation agent for cottonseed meal detoxification and preparation method and application thereof
A technology for microbial starter and cottonseed meal, applied in the field of starter, can solve the problems of high cost, unfavorable industrialized use, etc., and achieve the effects of low cost, reduction of fecal odor and harmful gas emissions, and easy preservation.
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Embodiment 1
[0058] Step 1: Culture Saccharomyces cerevisiae (ACCC20065) on potato medium (PDA), subculture Bacillus subtilis (ACCC10619) on nutrient agar medium, observe the growth rate of the bacteria, and culture at 28°C for 36 hours; Saccharomyces cerevisiae colonies larger than 2mm and strains of Bacillus subtilis colonies with a diameter larger than 5mm are stored at 4°C for later use;
[0059] The second step: Inoculate the Saccharomyces cerevisiae strain obtained in the first step in potato medium (PDA), inoculate the Bacillus subtilis strain in nutrient agar medium, and inoculate the two strains at a constant temperature of 250 rpm Cultivate in a shaker at 28°C for 24 hours, take samples, and use the plate counting method to determine the total number of colonies. The strains with a total number of colonies greater than 2 billion / ml are used for seed production;
[0060] Step 3: Transfer the screened Bacillus subtilis and Saccharomyces cerevisiae into eggplant bottles equipped wit...
Embodiment 2
[0070] Step 1: Cultivate Saccharomyces cerevisiae (ACCC20065) on potato medium (PDA), subculture Bacillus subtilis (ACCC10619) on nutrient agar medium, observe the growth rate of the strain, and cultivate at 30°C for 36 hours to reduce the diameter of 2mm Saccharomyces cerevisiae colonies, strains of Bacillus subtilis colonies with a diameter greater than 5mm are preserved at 4°C;
[0071] The second step: Inoculate the Saccharomyces cerevisiae strain obtained in the first step in potato medium (PDA), inoculate the Bacillus subtilis strain in nutrient agar medium, and inoculate the two strains at a constant temperature of 250 rpm Cultivate in a shaker at 30°C for 24 hours, take samples, and use the plate counting method to determine the total number of colonies. The strains with a total number of colonies greater than 2 billion / ml are used for seed production;
[0072] Step 3: Transfer the screened Bacillus subtilis and Saccharomyces cerevisiae into eggplant bottles equipped w...
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