Neisseria gonorrhoeae agar plate and preparation method thereof
An agar plate, gonococcus technology, applied in the field of culture medium, can solve problems such as poor gonococcus culture effect, excessive heating, affecting product quality and the like
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[0032] The embodiment of the present invention also provides a kind of preparation method of above-mentioned Neisseria gonorrhoeae agar plate, it comprises:
[0033] S1. Mix the tryptone, the animal peptone, the sodium chloride, the niacin, the yeast extract powder, the beef heart extract powder, the agar, and the water, and heat to Dissolve at 80~90°C to obtain premix A;
[0034] S2. Mix the cornstarch with the remaining water, heat to 130-135°C to dissolve, and obtain the premix B;
[0035] S3. Mixing the premix A and the premix B to obtain the culture solution;
[0036] S4. Sterilizing the culture solution at 120-125°C for 20-40 min;
[0037] S5. cooling the sterilized culture solution to 45-50°C and mixing it with the defibrated horse blood to obtain a mixed solution;
[0038] S6. heating the mixed solution at 80-85°C for 5-10 min, then cooling down to 60-70°C and continuing heating for 0.5-1 h to obtain the plate stock solution;
[0039] S7. Pour the plate stock solut...
Embodiment 1
[0048] This embodiment provides a Neisseria gonorrhoeae agar plate, which is obtained by mixing culture solution and defibrated horse blood, heating, cooling and solidifying. Wherein, in parts by weight, the culture solution includes:
[0049] 8 parts of tryptone, 4 parts of animal peptone, 3 parts of corn starch, 0.5 parts of niacin, 6 parts of sodium chloride, 2 parts of yeast extract powder, 4 parts of beef heart extract powder, 13 parts of agar, and 900 parts of water.
[0050] The volume ratio of culture medium and defibrated horse blood is 1:0.08.
[0051] The preparation method of this Neisseria gonorrhoeae agar plate is as follows:
[0052] S1. Mix tryptone, animal peptone, niacin, sodium chloride, yeast extract powder, agar, and 70% water, heat to 90°C to dissolve, and obtain premix A.
[0053] S2. Mix cornstarch with 30% water, heat to 130°C to dissolve, and obtain premix B.
[0054] S3. Mix the premix A and the premix B to obtain a culture solution, and adjust th...
Embodiment 2
[0062] This embodiment provides a Neisseria gonorrhoeae agar plate, which is obtained by mixing culture solution and defibrated horse blood, heating, cooling and solidifying. Wherein, in parts by weight, the culture solution includes:
[0063] 4 parts of tryptone, 8 parts of animal peptone, 1 part of corn starch, 2 parts of niacin, 4 parts of sodium chloride, 0.5 parts of yeast extract powder, 8 parts of beef heart extract powder, 18 parts of agar, and 1000 parts of water.
[0064] The volume ratio of culture medium and defibrated horse blood is 1:0.1.
[0065] The preparation method of this Neisseria gonorrhoeae agar plate is as follows:
[0066] S1. Mix tryptone, animal peptone, niacin, sodium chloride, yeast extract powder, agar, and 60% water, heat to 80°C to dissolve, and obtain premix A.
[0067] S2. Mix cornstarch with 40% water, heat to 120°C to dissolve, and obtain premix B.
[0068] S3. Mix the premix A and the premix B to obtain a culture solution, and adjust the...
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