A Bacillus pumilus and its Application in Controlling Earthy Odor in Liquor
A technology of Bacillus pumilus and BP-1, which is applied to the preparation of bacteria, alcoholic beverages, and methods based on microorganisms. It can solve the problems of destroying the micro-ecological structure, affecting the aroma and quality of liquor, and not being able to apply it.
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Embodiment 1
[0031] 1. Screening and isolation of Bacillus pumilus BP-1:
[0032]Use a sterile spatula to take 1g of Daqu koji powder at different stages and different koji positions into a 5ml sterile plastic centrifuge tube. Add 5ml of normal saline (0.9% sodium chloride solution) to the centrifuge tube, vortex for 2 minutes, let it stand for 10 minutes, draw 2 μl of spot seed coated with Streptomyces S.albus, S.fradiae, S.radiopugnans, S. The center of the PDA plate of sampsonii spores (containing 200g of potato boiled liquid, 20g of glucose, added distilled water to make the volume to 1L, and added 15g of agar) was cultivated in a constant temperature incubator at 30°C for 72h, and the size of the inhibition zone in the center of the plate was detected. Select the bacterium colony with the largest inhibition zone and draw a line on the PDA plate to isolate a single bacterial species, and spot the center of the PDA plate coated with Streptomyces S.albus, S.fradiae, S.radiopugnans, and S...
Embodiment 2
[0039] Example 2: Application detection of Bacillus pumilus inhibiting the growth of Streptomyces and the production of geosmin
[0040] 1. Mixed culture of Bacillus pumilus BP-1 and geosmin-producing Streptomyces S.albus
[0041] The isolated bacillus pumilus bacterial strain and the streptomyces bacterial strain S.albus of producing geosmin are according to the ratio of 1:10000,1:1000,1:100,1:10,1:1 (correspondingly, the ratio of the bacillus pumilus bacterial strain The inoculum amounts were 0.1‰, 1‰, 1%, 10%, 100%) to inoculate potato-glucose liquid medium, and cultured on a constant temperature shaker at 30° C. at 200 rpm for 50 h. After the fermentation, take 1ml of the bacterial liquid and centrifuge to collect the bacterial cells for the determination of the biomass of Streptomyces strain S.albus under mixed culture. The remaining fermentation liquid was centrifuged at 10,000 g to remove bacteria, and after being sterilized by filtration through a 0.22 μm microporous ...
Embodiment 3
[0052] Example 3: Application detection of antibacterial active components of Bacillus pumilus BP-1 antagonizing geosmin-producing Streptomyces and geosmin production
[0053] 1. The cultivation of geosmin-producing Streptomyces S.albus with the addition of Bacillus pumilus antibacterial active components
[0054] The antibacterial active components 3, 4 and components 5 and 6 separated by HPLC were added to the potato-glucose liquid medium of Streptomyces strain S. The second group is to add an equal volume of methanol. After the fermentation, take 1ml of the bacterial liquid and centrifuge to collect the bacterial cells for the determination of the biomass of Streptomyces strain S.albus. The remaining fermentation liquid was centrifuged at 10,000 g to remove bacteria, and after being sterilized by filtration through a 0.22 μm microporous membrane, a sterile fermentation liquid was obtained, which was stored at 4°C for later use.
[0055] 2. qPCR detection of Streptomyces S...
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