Improved formulation of blood agar culture medium
A medium and blood agar technology, applied in the field of bioengineering, can solve the problems of poor repairing ability of damaged bacteria, not very comprehensive and balanced nutrient agar, and not very suitable, so as to repair damaged bacteria, facilitate cultivation and identification, The effect of maintaining osmotic pressure
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Embodiment 1
[0016] The improved formula of the blood agar medium provided in this example is composed of tryptone, beef extract powder, liver digestate, yeast extract, starch, sodium chloride, defibrated sheep blood and agar, wherein: in every 1000ml medium, Contains tryptone 15g, beef extract powder 5g, liver digestate 2.5g, starch 1g, yeast powder 5g, sodium chloride 5g, defibrated sheep blood 50ml, agar 15g, pH=7.2±0.2.
[0017] The preparation steps of the above-mentioned medium are as follows: mix tryptone, beef extract powder, liver digestate, starch, yeast extract powder, sodium chloride, and agar in proportion, add purified water to a constant volume and heat to dissolve, and adjust the pH value to 7.2±0.2 , sterilized at 121°C for 15 minutes, cooled to 50°C, added sterile defibrinated sheep blood in proportion, mixed well, poured into the plate, condensed to obtain the finished medium, and set aside.
[0018] The new blood agar basal medium prepared by using the above components ...
Embodiment 2
[0025] The difference between this example and Example 1 is that every 1000ml of medium contains 12g of tryptone, 4g of beef extract powder, 3g of liver digestate, 1.5g of starch, 6g of yeast powder, 6g of sodium chloride, and 45ml of defibrated sheep blood , Agar 12g, pH=7.2±0.2.
Embodiment 3
[0027] The difference between this example and Example 1 is that each 1000ml of culture medium contains 18g of tryptone, 6g of beef extract powder, 1.5g of liver digestate, 0.5g of starch, 4g of yeast powder, 4g of sodium chloride, and defibrated sheep blood. 55ml, 18g agar, pH=7.2±0.2.
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