Method for detecting quantity of bacterium lacticum in mixed probiotic products
A technology of lactobacilli and probiotics, applied in the field of health care products, can solve the problems of unspecified detection and counting methods of lactobacilli in mixed probiotics, negative values and large deviations in results, and inability to perform accurate detection, etc., to achieve effective detection and Effects of controlling, removing interference, and filling gaps in detection
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[0073] Take 24 batches of mixed probiotic samples (containing Bifidobacteria and Lactobacillus), weigh 25g of mixed probiotic powder for each batch of samples, put them in a homogenization cup or a 500mL centrifuge tube + glass beads, add 225mL sterile normal saline accurately, and mix For 5 minutes, take 1mL sample homogeneous solution, add it to 9mL sterile normal saline, and make 10-fold incremental dilution, choose 2~3 continuous appropriate dilutions, and draw 1mL sample homogeneous solution into a sterile petri dish for each dilution. Make two plates for each dilution. After the dilution is transferred into the plate, pour about 15mL of the MRS agar medium cooled to 48°C into the plate, rotate the plate to mix evenly, and incubate aerobically at 36°C±1°C for 72h±2h. After counting the number of all colonies on the plate to obtain the lactobacillus, it should be completed within 15 minutes from sample dilution to plate pouring, and the test results are shown in Table 2.
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