Method for effectively killing viable but nonculturable state microorganisms generated in ultrasonic sterilization process
A technology of microbes and ultrasound, applied in the field of food engineering, can solve problems that are not involved, endanger food safety, etc., achieve the effect of promoting industrial application and optimizing the ultrasonic sterilization process
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Embodiment 1
[0023] Ultrasonic combined with weak acid potential water treatment
[0024] (1) Preparation of bacterial suspension
[0025] The Staphylococcus aureus standard strain ATCC 25923 was inoculated in ordinary broth medium, and cultured on a shaker at 37°C until the logarithmic growth phase.
[0026] Experimental group: Wash the bacteria in the logarithmic growth phase twice with 0.85% sterile saline, and then resuspend the bacteria in 2mg / mL weakly acidic water, so that the concentration of the bacteria is about 10 8 CFU / mL, as the bacterial suspension of the experimental group;
[0027] Control group: Wash the bacteria in the logarithmic growth phase twice with 0.85% sterile normal saline, then resuspend the bacteria in 0.85% sterile normal saline, so that the concentration of the bacteria is about 10 8 CFU / mL, as the bacterial suspension of the control group;
[0028] (2) Ultrasonic treatment
[0029] Immediately process the suspension of Staphylococcus aureus with an ultra...
Embodiment 2
[0039] Ultrasonic combined with weak acid potential water treatment
[0040] (1) Preparation of bacterial suspension
[0041] Same as the method of step (1) in Example 1.
[0042] (2) Ultrasonic induction
[0043] The method of one step (2) in embodiment 1 is basically the same, only the processing time is changed to 10min.
[0044] Two detection
[0045] Same as the method of two in embodiment 1.
[0046]The results are as follows: the ratio of viable Staphylococcus aureus in the experimental group was 0.09%, the ratio of cultivable bacteria was 0.021%, and the ratio of live bacteria in non-culturable state was 0.069%. The ratio of viable Staphylococcus aureus in the control group was 89.40%, the ratio of cultivable bacteria was 43.65%, and the ratio of live bacteria in non-culturable state was 45.75%. It can be seen that the method of the present invention killed a large proportion of living non-culturable bacteria when the combined treatment was performed for 10 minute...
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