Culture medium to detect Bifidobacterium and quick detection and counting method
A bifidobacterium and culture medium technology, which is applied in the field of detection of bifidobacteria culture medium and rapid detection and counting, can solve the problems of inability to intuitive and convenient detection and counting, large colony growth of bifidobacteria, inaccurate colony counting, etc.
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preparation example 1
[0087] Preparation example 1: A kind of experimental suspension liquid, get the standard bacterial strain Bifidobacterium longum that is activated, Bifidobacterium breve, Bifidobacterium infantis, Bifidobacterium adolescent, Bifidobacterium bifidum, Bifidobacterium animalis, Lactobacillus acidophilus, Streptococcus thermophilus, Lactobacillus bulgaricus, Salmonella, Staphylococcus aureus and Escherichia coli were added to sterile saline to make a bacterial suspension, and the turbidity reached 0.5 through the turbidimeter test McFarland units to obtain the experimental suspension.
preparation example 2-13
[0088] Preparation Example 2-13: An experimental suspension, which is different from Preparation Example 1 in that its components and dosage are different, and the unit of turbidity is the McFarland unit, see Table 1 for details.
[0089] Table 1 Preparation Example Experimental Suspension Liquid 2-13 Bacteria Selection
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preparation example 14
[0093] Preparation Example 14: A basal medium, the preparation method of which is as follows: 10.0 g of peptone, 8.0 g of beef extract powder, 4.0 g of yeast extract powder, 20.0 g of glucose, 2.0 g of dipotassium hydrogen phosphate, and 2.0 g of diammonium hydrogen citrate , sodium acetate 5.0g, magnesium sulfate 0.2g, manganese sulfate 0.04g, add distilled water directly to 1L, heat slightly to dissolve completely, then add the chromogenic substrate 5-bromo-4-chloro-3 indole-α - 20mg of D-galactoside, after mixing, adjust the pH to 5.5±0.2 at 25°C, finally add 11g of agar, boil to dissolve it completely, cool to about 50°C and keep warm.
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