Bacillus subtilis viable count medium, diluent and viable count method
A technology for counting Bacillus subtilis and viable bacteria, applied in the direction of microorganism-based methods, biochemical equipment and methods, instruments, etc., can solve the problems of high bacterial cell death rate, excessive foam, and excessive colonies on the counting plate, and reduce the Mortality, reduced foam formation, and improved counting accuracy
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Embodiment 1
[0050] Embodiment 1, Bacillus subtilis viable count solid culture medium of the present invention
[0051] The solid medium of the present invention (formula 1): 4g of peeled soybean meal powder (crushed to 100 mesh), 3g of corn flour (crushed to 100 mesh), 5g of sodium chloride, 3g of xanthan gum, 13g of agar, 1000mL of distilled water, pH value is 7.3.
[0052] The solid medium of the present invention (formulation 2): 6g of peeled soybean meal powder (crushed to 100 mesh), 5g of corn flour (crushed to 100 mesh), 10g of sodium chloride, 5g of xanthan gum, 11g of agar, 1000mL of distilled water, pH value is 7.5.
Embodiment 2
[0053] Embodiment 2, Bacillus subtilis live bacteria count sterilization diluent of the present invention
[0054] The sterilizing diluent of the present invention (Formulation 1): 8 g of sodium chloride, 2 g of potassium dihydrogen phosphate, 0.3 g of anhydrous glucose, 0.3 g of peptone, 0.1 g of polyoxypropylene oxide glycerol ether defoamer, and 1000 mL of distilled water.
[0055] The sterilizing diluent of the present invention (formula 2): 9 g of sodium chloride, 2 g of potassium dihydrogen phosphate, 0.5 g of anhydrous glucose, 0.5 g of peptone, 0.2 g of polyoxypropylene oxide glycerol ether defoamer, and 1000 mL of distilled water.
Embodiment 3
[0056] Embodiment 3, Bacillus subtilis viable count method of the present invention
[0057] Sample: Bacillus subtilis sample, the number of viable bacteria is about 5.0×10 10 CFU / g.
[0058] S1: Preparation of initial suspension:
[0059] Weigh 25g of the sample by aseptic operation, add 225mL of sterilized diluent, add 50 sterilized glass beads, shake for 30min, and make an initial suspension of 1:10.
[0060] S2: ten-fold serial dilution:
[0061] Prepare a vial with a capacity of 15 mL, add 9 mL of sterilized diluent and 10 sterilized glass beads into it, draw 1 mL of the initial suspension obtained in step S1 into the vial, vibrate with a vortex oscillator for 20-30 s, and make 1 : 100 dilution I, and the resulting dilution I is then subjected to ten-fold serial dilutions, respectively gradient dilution to a dilution of 10 7 , 10 8 , 10 9 ;
[0062] S3: Spread plate culture:
[0063] The dilution obtained in step S2 is 10 7 , 10 8 , 10 9 The diluted solution w...
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