Preparation method of high-yielding acetoin and aroma-enhancing Bacillus mohaiwei direct-throwing starter and its application in the production of Shanxi aged vinegar
A technology of direct-throwing fermentation agent and Bacillus vegiturus, applied in the field of microorganisms, can solve the problems of less research on the development and application of Bacillus
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Embodiment 1
[0018] Example 1: Screening of high-yielding acetoin, polyphenols and aromatizing spores
[0019] (1) Screening of high-yielding acetoin spores: the wine mash samples from the alcoholic fermentation stage of Shanxi old mature vinegar and the vinegar fermented grains samples from the acetic acid fermentation stage were collected respectively, diluted and coated with MRS medium, and finally 50 strains of spores were isolated . Voges-Proskauer (V-P) reaction and spectrophotometry were used to measure its acetoin-producing ability, and Bacillus 15 produced the highest acetoin at 45.63g / L; followed by Bacillus 297 (40.52g / L) and Bacillus 2030 (40.28g / L).
[0020] The preparation method of the above-mentioned MRS solid medium is: peptone 10g, beef extract 10g, yeast extract 5g, K 2 HPO 4 2g, sodium acetate 2g, triammonium citrate 2g, glucose 20g, Tween 80 1mL, MgSO 4 0.2g, MnSO 4 0.05g, 20g agar, 1000mL distilled water, adjust the pH to 6.2‒6.6, and sterilize at 121°C for 20m...
Embodiment 2
[0047] Example 2: Strain identification of high-yielding acetoin, polyphenols and Aromaspora 15
[0048] Morphological identification: Pick up 15 spores with an inoculation loop and streak on the MRS plate medium to isolate a single colony, take pictures of the colonies grown on the medium, record them, and then check by Gram staining microscope. Observe its cell morphology. Bacillus 15 formed a colony with a diameter of 4.80mm on the MRS plate medium, with irregular edges, rough surface and obvious wrinkles, translucent, dry, ridge-like protrusions in the middle, slightly viscous, and light yellow; its cell shape: leather Ran's staining was G + , rod-shaped, with spores in the middle, such as figure 1 shown.
[0049] 16Sr DNA sequencing: the genome of Bacillus 15 was extracted with a kit, and the 16Sr DNA sequencing and strain identification were carried out. The primers were: upstream: 5′-CAGATGGGAGCTTGCTCCCTG-3′ downstream: 5′-CGACTTCACCCAATC
[0050] ATCTG-3′, using B...
Embodiment 3
[0051] Embodiment 3: the preparation of Bacillus mohewei CGMCC 16910 direct throw type starter
[0052] The activated Bacillus mohewei CGMCC 16910 was inoculated into the MRS medium at an inoculation amount of 3%, and after 24 hours of cultivation at 37°C and 180 r / min, the concentration of the bacteria reached 10 8 cfu / mL, use a hollow fiber membrane to concentrate the fermentation broth of Bacillus mohaiwei to 1 / 5 of the original volume, add a sterile protective agent to the concentrated fermentation broth, and the volume ratio of the concentrated fermentation broth to the protective agent is 1:3 (v: v) Mixing, processing the fermented liquid by low-temperature spray drying, and then vacuum-packing to obtain the Bacillus mohaiwi direct-throwing starter.
[0053] The preparation method of the above protective agent is: A: 10 g of skim milk powder, 100 mL of distilled water, sterilized at 115 °C for 15 min; B: 1.5 g of trehalose, 0.5 g of glycerin, 2 g of sorbitol, 1 g of malt...
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