Antibacterial agent for restraining shewanella putrefaciens, preparation method of antibacterial agent, and application of antibacterial agent to preparation of antistaling agent for south America white shrimps
A technology of Shewanella putrefaciens and antibacterial agents, which is applied in the field of antibacterial agents of Shewanella putrefacci, achieving high safety, high efficiency, simple and easy to control process cost, and good effect
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specific Embodiment 1
[0044] 1. Extraction method of total flavonoids
[0045] (1) Take 1,000 g of dried cabbage powder and pass through a 60-mesh sieve, add 40 L of 70% ethanol solution, homogenize, and extract with ultrasonic assistance. The ultrasonic time is 60 min, the ultrasonic temperature is 60 ℃, and then leached for 2 h , the extraction temperature was 60°C, and the supernatant was obtained by filtration;
[0046] (2) Concentrate the supernatant obtained in step (1) under reduced pressure, recover the solvent, and heat at a temperature of 45-50°C. After the concentration is completed, add anhydrous ethanol twice the volume of the concentrate;
[0047] (3) Treat the solution obtained in step (2) at a low temperature of 4°C for 24 h, filter, remove the precipitate, and take the supernatant;
[0048] (4) Concentrate the supernatant obtained in step (3) under reduced pressure, recover the solvent, and heat at a temperature of 45-50°C. After the concentration is completed, use the aluminum ch...
specific Embodiment 2
[0056] 1. Determination of minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC)
[0057] Dilute the total flavonoids prepared in Example 1 by two-fold dilution method, add it to the nutrient agar medium and mix well, pour it into a petri dish respectively, and after it solidifies, cultivate 0.1 mL of putrefied Schwarzwald until the logarithmic phase The bacterial suspension was spread on each petri dish, and sterile water was used as the control. After culturing at 30 °C for 24 h, the growth of the colony was observed. The minimum concentration of flavonoids with complete aseptic growth was taken as the minimum inhibitory concentration. Continue to cultivate at 30 ℃, and after 48 h, the minimum concentration of flavonoids with no colony growth is the minimum bactericidal concentration. The experimental results are shown in Table 1 and Table 2 below,
[0058] Table 1 The MIC of flavin ketones to Shewanella putrefaciens
[0059] .
[0060] Tab...
specific Embodiment 3
[0079] Shrimp preservation treatment method: collect fresh and healthy Penaeus vannamei, add oxygen and water to keep them alive, and transport them back, remove dead, discolored, incomplete limbs and other abnormal individuals, rinse them with sterile water, put them in crushed ice to make them die suddenly, the ratio of volume The ratio is 1:3; soak the treated Penaeus vannamei in preservative for 20 minutes. Drain the residual fresh-keeping agent of Penaeus vannamei after soaking, and use aseptic wind to assist draining. The temperature requirement is about 4°C, and the wind speed is 1.5 m / s. After draining, put it into a sterile fresh-keeping bag. Vannamei shrimp were stored in a 4°C incubator. Wherein the vannamei preservatives are respectively
[0080] The antistaling agent of the treatment method of the present invention: it is composed of the following raw materials and parts by weight: 4 parts of total flavonoids of cabbage, 2 parts of blueberry leaf polyphenols, 3.2...
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