Method for determining colony count of pathogenic microbes in dehydrated garlic product
A technology of pathogenic microorganisms and the total number of colonies, which is applied in the field of microbial detection, can solve the problems that are not suitable for the safety and sanitation detection of dehydrated garlic products, and achieve the effect of rapid detection and simple steps
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Embodiment 1
[0014] 1 Materials and instruments
[0015] 1.1 Materials
[0016] Salmonella species ( salmonella ) is provided by Beijing Lanbo Rui Company, various culture media are provided by Beijing Luqiao Company, Ciba series food-grade polyacrylamide cationic resin, and the samples are from Anhui Donggan Food Co., Ltd. for inspection samples;
[0017] 1.2 Instruments
[0018] Desktop high-speed refrigerated centrifuge (BECKMAN 64R), vertical high-speed refrigerated centrifuge (BECKMAN J30I), micro-sampler: 0.5 ul~10ul, 10 ul~100ul, autoclave.
[0019] 2 Bacteria removal rate experiment
[0020] Weigh 25g of dehydrated garlic product sample (sterilized by irradiation), manually add one McFarland unit (3.5×10 8 Individuals / g) Salmonella strains, add 225mL sterilized diluent to homogenize, filter with a homogeneous bag with a filter membrane, the filter membrane has a pore size of 330μm and a diameter of 50mm; absorb the clear liquid, and divide 1.5mL clear liquid into two 2m...
Embodiment 2
[0026] 1 material and instrument are identical with embodiment 1
[0027] 2 Comparison of the high-speed centrifugation method for the determination of the total number of colonies and the traditional method
[0028] Take 25g of garlic powder sample, add 225mL of sterilized diluent, homogenize and filter through a homogeneous bag with a filter membrane, absorb the clear liquid, and divide 1.5mL into two 2mL centrifuge tubes; Add a small amount of polyacrylamide cationic resin into the centrifuge tube as a coagulant aid, and the concentration of the coagulant aid in the supernatant is 0.1ppm; centrifuge for 40 minutes at a temperature of 4°C and a speed of 20,000 rpm, remove the supernatant, and remove the supernatant in the sediment Add 1.5 mL of sterile distilled water and mix well, measure the amount of bacteria in the sediment according to the national standard GB 4789.2-2010, and use the standard method for comparison; other conditions are the same as in Example 1.
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