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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

Inactive Publication Date: 2020-02-04
中秀科技股份有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] The existing Neisseria gonorrhoeae agar medium is not very comprehensive and uniform in nutrient composition, and the effect on the cultivation of Neisseria gonorrhoeae is not good
Moreover, the existing method for preparing Neisseria gonorrhoeae agar is more suitable for small-scale self-production and self-use. During large-scale production, there will be agglomeration, overheating, etc., which will affect product quality.

Method used

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Examples

Experimental program
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Effect test

preparation example Construction

[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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Abstract

The invention discloses a Neisseria gonorrhoeae agar plate and a preparation method thereof, and relates to the technical field of culture medium. The Neisseria gonorrhoeae agar plate is more comprehensive in nutrition and capable of effectively promoting the growth of Neisseria gonorrhoeae and improving the separation rate of Neisseria gonorrhoeae. According to the preparation method, corn starchis separated to be subjected to high temperature dissolution since the corn starch is not easy to dissolve, thus ensuring the dissolving efficiency and avoiding the nutrient damage to other components caused by high temperature. Meanwhile, after high temperature sterilization of the culture medium, the mixed solution is subjected to heating hematolysis, so that the V factor and the X factor in red blood cells are released. During heating, a short time heating is carried out at a higher temperature to promote the rapid rupture of cell walls, and then a continuous heating is carried out at a lower temperature to ensure the full release of substances in the red blood cells and avoid the damage to other nutrient substances by high temperature. The preparation method is simple to operate, lowin requirements on equipment, capable of effectively improving product quality and suitable for industrial production.

Description

technical field [0001] The invention relates to the technical field of medium, in particular to a gonorrhoeae agar plate and a preparation method thereof. Background technique [0002] Pathogenic bacteria or opportunistic pathogenic bacteria exist in the infected site, leading to common clinical infections, such as respiratory tract infection, reproductive tract infection, intestinal infection, etc. In order to accurately diagnose the type of bacteria in the infected site, patients are often used clinically Samples are collected from the site for culture, and clinical examiners select suspicious strains for identification based on clinical symptoms, so as to determine the type of infected bacteria in the patient's site and provide a basis for clinical treatment. Diagnosis and culture of infected bacterial types in patient parts are currently the only feasible methods in clinical diagnosis. Other methods, such as immune antigen detection and nucleic acid detection, are not su...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12N1/20C12R1/01
CPCC12N1/20
Inventor 孙月鹏张娟丽吕斌谭韦丽罗江卫
Owner 中秀科技股份有限公司
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