Microbial flocculant for clarifying brewed vinegar and preparation method and application thereof
A microbial flocculant, a technology for brewing vinegar, applied in the field of microbial engineering
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Embodiment 1
[0024] Paenibacillus castaneae was first activated on the test tube slant before inoculation, and cultivated at 28°C for 48 hours. The slant medium used for cultivation consisted of: 2.0% soluble starch, 0.5% peptone, 0.05% potassium chloride, hydrogen phosphate Dipotassium 0.1%, magnesium sulfate 0.05%, agar 2.0%, pH 7.0; Then the bacterial cells were washed with sterile water and inserted into a triangular flask (500mL) containing 100mL seed culture solution for seed culture (cultivated at 28°C for 30 hours ), the medium is 1.0% soluble starch, 1.5% sucrose, 0.5% peptone, 0.05% potassium chloride, 0.1% dipotassium hydrogen phosphate, and 0.05% magnesium sulfate. After the seed growth is completed, the microscopic examination is free of bacteria for later use.
[0025] 7L of fermentation medium was prepared, and the formula of the medium was 3.0% of glucose, 0.1% of sodium nitrate, 0.3% of peptone, 0.05% of potassium chloride, 0.1% of dipotassium hydrogen phosphate, and 0.05%...
Embodiment 2
[0028] Example 2: Optimization of microbial flocculant application conditions in brewing vinegar
[0029] 1. Method for determination of flocculation effect of vinegar
[0030] The submerged liquid fermented vinegar was collected, and the permeability was used as an index to measure the flocculation effect of the purified bioflocculant in rice vinegar. Add 1 mL of the purified bioflocculant solution to 100 mL of rice vinegar. Stir for 2 minutes, let stand for 10 minutes, and take the supernatant for analysis. The transmittance of the supernatant was measured at a wavelength of 900 nm. The control group was prepared according to the same process except that the sample solution was used instead of distilled water.
[0031]The increase rate of transmittance (Increase rate of transmittance, IRT) is calculated as follows:
[0032]
[0033] A: initial value; B: value after flocculation treatment
[0034] 2. Single factor optimization method for vinegar flocculation condition...
Embodiment 3
[0050] Embodiment 3: the product safety test that the inventive method prepares
[0051] 1. Acute oral toxicity test in mice
[0052] Evenly disperse the prepared sample homogenizer in distilled water at 70°C, and prepare the concentration to be 0.1g·ml -1 solution, cooled to 40°C for later use. Select clean-grade ICR mice, weighing 18-24g, 10 males and 10 males, fasted for 16 hours before gavage, and give the test substance three times within 24 hours after weighing, with a gavage volume of 40ml kg -1 , with a cumulative total dose of 12 g·kg -1 . They were given food 4 hours after gavage, observed continuously for 14 days, and recorded the symptoms of poisoning and death.
[0053] Table 3 Body weight gain record of acute toxicity mice
[0054]
[0055] Note: * is significantly different from the control group (P<0.05), ** is very significantly different from the control group (P<0.01)
[0056] After administration, the mice had bright coat, no excitement, restlessne...
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