Food and tableware coliform bacteria rapid detection scrip preparation and application
A technology of coliform bacteria and paper chips, which is applied in the direction of biochemical equipment and methods, and microbial measurement/inspection, etc., can solve problems such as the inability to use tableware for coliform bacteria detection, difficult colony counting, and unclear colony formation, etc., to achieve Low cost, accurate results, effect of reducing interference effects
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Embodiment 1
[0028] Embodiment 1: the preparation method of rapid detection test strip
[0029] (1) Preparation of carrier paper sheets: cut the chromatographic filter paper into 5cm×5cm size, irradiate or autoclave (after high pressure, dry at constant temperature and vacuum at 50°C) for later use.
[0030] (2) Preparation of the inner packaging bag: Press the high-temperature-resistant polypropylene plastic film bag into a joint bag with a size of 5.1cm×5.1cm according to the test requirements.
[0031] (3) Basic medium configuration (1L): tryptone 10.0-15.0g; beef extract 3.0-5.0g; sodium chloride 5.0-6.0g dipotassium hydrogen phosphate (K 2 HPO 4 2H 2 O) 4.0-5.0 g; lactose 15.0-20.0 g; bromocresol purple content 60.0-70.0 mg; deoxycholic acid content 1.0-1.5 g; 20.0g / L red tetrazolium (TTC) solution 5-7 mL.
[0032] (4) Cold water gel configuration (mass percentage): 0.2-0.4% sodium polyacrylate, 0.1-0.3% xanthan gum, 0.1-0.2% carrageenan and 0.1-0.2% konjac gum.
[0033] (5) ...
Embodiment 2
[0036] Embodiment 2: the specificity test of rapid detection test strip
[0037] Cultivate Bacillus subtilis, Staphylococcus aureus, Salmonella, Vibrio parahaemolyticus, and Listeria monocytogenes overnight in shake flasks, centrifuge 1 mL of the bacterial suspension at 8000 r / min for 5 min, resuspend the bacterial cells in 1 mL of sterile water, According to the ten-fold dilution, dilute to a certain multiple (10 3 -10 4 ), drop 1mL of the bacterial suspension onto the test paper, incubate at 36°C±1°C for 16-24h, observe the growth of the colony on the paper, and study the specificity of the test paper. 5 parallel groups were set up, and the experiment was repeated 3 times.
[0038]The test results show that only when Escherichia coli exists, the test strip will turn yellow and show red spot colonies or flaky blush on the yellow background; while Bacillus subtilis, Staphylococcus aureus, Salmonella, Vibrio parahaemolyticus, When Listeria monocytogenes is present, the ...
Embodiment 3
[0039] Embodiment 3: the interfering test of rapid detection test strip
[0040] At the same time, Escherichia coli, Bacillus subtilis, Staphylococcus aureus, Salmonella, Vibrio parahaemolyticus, and Listeria monocytogenes were cultured overnight in shake flasks, and 0.5mL of the bacterial suspension was centrifuged at 8000r / min for 5min. to a certain multiple (10 3 -10 4 ), followed by mixing 0.5ml of Bacillus subtilis, Staphylococcus aureus, Salmonella, Vibrio parahaemolyticus, and Listeria monocytogenes with 0.5ml of Escherichia coli suspension, resuspended in 1mL of sterile water, Add 1mL of bacterial suspension dropwise to the detection paper, incubate at 36°C±1°C for 16-24 hours, observe the growth of colonies on the paper, and study whether other bacteria interfere with the growth of E. coli. 5 parallel groups were set up, and the experiment was repeated 3 times.
[0041] The test results show that as long as E. coli exists in the mixed bacterial solution, the t...
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