Preparation method for blue-green algae single-cell protein feed
A single-cell protein, cyanobacteria technology, applied in animal feed, animal feed, applications, etc., can solve the problems that the feed industry and aquaculture industry are difficult to accept and promote, the product has high salt content, and the production cost is high, and achieves significant dehydration and energy saving effect. , the effect of rich fermentation products and high internal quality
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Embodiment 1
[0029] The preparation of embodiment 1 Aspergillus niger
[0030] The Aspergillus niger used in this application comes from the Institute of Microbiology, Chinese Academy of Sciences. After domesticating and adapting the strain to cyanobacteria, the applicant obtained a new strain that can improve single-cell protein, increase fermentation dehydration rate and resist miscellaneous bacteria pollution. Aspergillus niger, the applicant has deposited the new strain of Aspergillus niger in the General Microbiology Center of China Committee for the Collection of Microorganisms on December 27, 2013. The address is: No. 3, Courtyard 1, Beichen West Road, Chaoyang District, Beijing, Institute of Microbiology, Chinese Academy of Sciences, Zip Code: 100101, the deposit number is CGMCC No.8640.
Embodiment 2
[0031] Example 2 Preparation of Cyanobacteria Dehydration Filter Block
[0032] The cyanobacteria collection liquid with a water content above 98% is carried out by a pressurized dissolved air flotation machine for pressurized air flotation, and then press-filtered with a sludge filter press to obtain a cyanobacteria dehydration filter block with a water content of 79%-87.2%.
Embodiment 3
[0033] Embodiment 3 Cyanobacteria solid-state fermentation prepares single-cell protein feed
[0034] The medium involved in this embodiment:
[0035] The solid medium formula is bran and water with a mass ratio of 1-1.5;
[0036] Cha's medium formula: add 3g NaNO to 1L distilled water 3 , 1g K 2 HPO 4 , 0.5g KCL, 0.5g MgSO 4 ﹒ 7H 2 O, 0.01g FeSO 4 ﹒ 4H 2 O, 30g sucrose and 15-20g agar, adjust the pH to be 6.0-6.5.
[0037] Get the Aspergillus niger obtained in Example 1 and inoculate it on the Cha's culture medium for activation, culture it on a slope at 28-30°C for 3-5 days, after the slope is covered with colonies, pick a colony, and inoculate it on the Krebs In Pingcha's medium, expand the slope at 28-30°C for 3-4 days, wait until the slope is covered with colonies, add sterile water to scrape the colonies on the slope to make a bacterial suspension, and use 3ml of Aspergillus niger as a solution of Aspergillus niger. 1×10 6 -1×10 8 The cfu / ml Aspergillus ...
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