Cold water gel test paper sheet for rapid detection of Listeria monocytogenes in food and tableware and its preparation method and application
A technology of Listeria monocytogenes and cold water gel is applied in the field of cold water gel test strips and preparation thereof, which can solve the problem that the detection of Listeria monocytogenes on the surface of tableware cannot be used, the quantitative detection requirements cannot be met, and only qualitative detection can be performed. Detection and other problems, to achieve the effect of low cost, strong specificity and high sensitivity
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Embodiment 1
[0046] Chromogenic agent (2R,3S,4R,5R,6R)-1,2,3,4,5-pentahydroxycyclohexyl-(2-nitro-4-fluorophenyl)phosphate is prepared as follows , including the following steps:
[0047] (1) Dissolve 1 mmol of reactant A (1,2,3,4,5,6-hexamethoxymethylene-inositol) in 2.5 mmol of anhydrous diisopropylamine and a small amount of anhydrous chloroform to obtain the reactant System A, and then freeze the reactant system A at -70°C;
[0048] (2) At a low temperature of -70°C, 1.25 mmol of reactant B (methyl dichlorophosphite) was added dropwise to the reactant A system in an anhydrous nitrogen atmosphere, vigorously stirred, and reacted for 6 hours;
[0049] (3) Place the system after the reaction in step (2) at room temperature. After the reaction system reaches room temperature, continue to add 2 mmol of reactant C (2-nitro-4-fluorophenol) dissolved in anhydrous Chloroform solution, continue to stir and react at room temperature for 12 hours to generate phosphite substances;
[0050] (4) Ad...
Embodiment 2
[0054] A kind of preparation method of listeria monocytogenes rapid detection cold water gel test paper sheet of the present embodiment, described method comprises the following steps:
[0055] (1) Preparation of carrier paper sheets: Cut the chromatographic filter paper into a size of 5 cm × 5 cm, irradiate or autoclave (after high pressure, dry at a constant temperature of 45° C. in vacuum) for later use;
[0056] (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;
[0057] (3) Preparation of basal medium (1L): Each liter of medium contains tryptone 5.0-6.0g, beef powder 5.0-6.0g, polyvalent peptone 3.0-5.0g, sodium chloride 8.0-10.0g, dihydrogen phosphate Potassium 1.0-1.5g, disodium hydrogen phosphate 5.0-7.0g, glycine 8.0-10.0g, lithium chloride 1.0-2.0g, phenylethyl alcohol 2.0-3.0g, escin 1.0-1.5g;
[0058] (4) The chromogen (2R, 3...
Embodiment 3
[0064] Embodiment 3 Rapidly detects the interfering test of test paper sheet
[0065] At the same time, shake flasks of Escherichia coli, Staphylococcus aureus, Salmonella, Vibrio parahaemolyticus, and Listeria monocytogenes were cultivated overnight, and 0.5mL of the bacterial suspension was centrifuged at 8000r / min for 5min, and diluted tenfold to A certain multiple (10 2 cfu / mL), followed by mixing 0.5 mL of Escherichia coli, Staphylococcus aureus, Salmonella, and Vibrio parahaemolyticus suspension with 0.5 mL of Listeria monocytogenes suspension, and resuspended in 1 mL of sterile water , drop 1mL of the bacterial suspension onto the detection paper, incubate at 36°C±1°C for 24-36h, observe the growth of the colonies on the paper, and study whether other bacteria interfere with the growth of Listeria monocytogenes, set up 5 parallel group, the test was repeated 3 times, and the test results showed that as long as there was Listeria monocytogenes in the mixed bacterial sol...
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