Strain for fermenting soybeans, fermentation agent containing same and use of same
A compound fermentation agent and strain technology, applied in the direction of application, microbe-based methods, bacteria, etc., to achieve the effects of convenient use, shortened koji making time, and good fermentation characteristics
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Embodiment 1
[0029] Embodiment 1: Isolation, screening and identification of strains
[0030] 1. Separation medium: preparation of beef extract peptone agar medium
[0031] Separation medium components: in g / L, peptone 10g, beef extract 3g, NaCl 5g, agar 15-17g, add distilled water to 1000mL, adjust the pH of the medium to 7.4. The culture medium was divided into Erlenmeyer flasks, sterilized under high-pressure steam of 0.1Mpa for 20min, and then used for later use.
[0032] 2. Separation method (dilution plate method)
[0033] 2.1 Preparation of sample diluent:
[0034] Use a 1ml sterile pipette to draw 1ml of the enriched culture solution (i.e. the above-mentioned separation medium), put it into a test tube filled with 9ml of sterile water, oscillate and mix well and serve as 10 -1 diluent; then use a 1ml sterile pipette to draw 10 -1 Put 1ml of the diluent into a test tube filled with 9ml of sterile water, blow and suck three times, let the bacteria solution mix evenly, and serve as ...
Embodiment 2
[0052] The preparation of embodiment 2 single strain fermentation agent (or claim bacterial agent)
[0053] 1. Test materials: Bacillus subtilis YDC-001 is a new bacterial strain isolated and screened by the present invention, Aspergillus oryzae A3042 is purchased from Institute of Microbiology, Chinese Academy of Sciences; glycerin; skim milk is a commodity.
[0054] 2. Production of Bacillus subtilis starter
[0055] 1) Cultivation of strains in inclined test tubes: inoculate Bacillus subtilis YDC-001 on beef extract peptone agar medium (the formula is the same as the separation medium in Example 1) and adjust the pH of the medium to about 6.0 before sterilization) on the inclined plane solid Above, cultivate it at 37°C for 1-2 days to activate it to become a slant strain.
[0056] 2) Erlenmeyer flask expansion culture
[0057] Enrichment liquid medium: 10g peptone, 3g beef extract, 5g NaCl, add distilled water to 1000mL, adjust the pH of the medium to 7.4 before steriliza...
Embodiment 3
[0081] The determination of the mixing ratio of embodiment 3 bacillus subtilis YDC-001 and aspergillus oryzae A3042 starter
[0082] 1. Test material
[0083] The test strains were Bacillus subtilis YDC-001 of the present invention and the commercially available strain Aspergillus oryzae A3042, and the soybean was a commercially available product.
[0084] 2. Determination of the proportion of mixed starter bacteria
[0085] The above-mentioned Bacillus subtilis YDC-001 starter and Aspergillus oryzae A3042 starter are mixed respectively according to the ratio of mass ratio 1: 1 or 1: 2 or 1: 3 to make composite starter (or claim composite starter ). According to the production process of Aspergillus fermented soya bean (document is the same as before), add 0.4% mass of different proportions of mixed starter respectively, after making koji, measure the protease activity of bean koji, and compare with the protease activity of the bean koji made by purebred Aspergillus oryzae ...
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