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Culture medium for separating fungi from yeast-like fungi and preparation method

A technology for yeast-like fungi and fungi separation, which is applied in the field of medical chemiluminescence immunoassay detection, can solve the problems of single component, unbalanced ratio of source and nitrogen source, and poor effect of separating some fungi, and achieves the effect of inhibiting growth.

Pending Publication Date: 2019-12-24
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

[0004] The present invention aims at the single carbon source and nitrogen source components in the culture medium for separating fungi, which is prone to imbalance in the ratio of source and nitrogen source. At the same time, a combination of various antibacterial agents is used to inhibit bacteria, so that the antibacterial effect is superimposed on some fungi. phenomenon, which leads to the problem of poor effect of separating some fungi, and provides a culture medium and preparation method for isolating fungi and yeast-like fungi

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0026] A preparation method for a medium for separating fungi and yeast-like fungi, comprising the following steps:

[0027] S1, formulation, in parts by weight, take 5 parts of tryptone, 5 parts of animal peptone, 30 parts of glucose, 0.3 part of chloramphenicol and 10 parts of agar and mix evenly, and add 900 parts of purified water to it to prepare a mixed Reagent;

[0028] S2, damp heat sterilization, the mixed reagent is placed in a humid heat environment, and heated at 120°C to 130°C for 30 minutes to perform moist heat sterilization to obtain the sterilized reagent;

[0029] S3, filling, filling the sterilized reagent into the sterilized culture bottle;

[0030] S4, drying and sealing, drying the filled culture bottle, and sealing it with a cap;

[0031] S5, spray code and seal the film, spray the information code on the surface of the culture bottle after plugging and capping, and seal the film;

[0032] S6, labeling, affixing a label on the surface of the sealed cu...

Embodiment 2

[0036] A preparation method for a medium for separating fungi and yeast-like fungi, comprising the following steps:

[0037] S1, formulation, in parts by weight, take 15 parts of tryptone, 15 parts of animal peptone, 50 parts of glucose, 0.7 part of chloramphenicol and 20 parts of agar and mix evenly, and add 1100 parts of purified water to it to prepare a mixed Reagent;

[0038] S2, damp heat sterilization, the mixed reagent is placed in a humid heat environment, and heated at 120°C to 130°C for 30 minutes to perform moist heat sterilization to obtain the sterilized reagent;

[0039] S3, filling, filling the sterilized reagent into the sterilized culture bottle;

[0040] S4, drying and sealing, drying the filled culture bottle, and sealing it with a cap;

[0041] S5, spray code and seal the film, spray the information code on the surface of the culture bottle after plugging and capping, and seal the film;

[0042] S6, labeling, affixing a label on the surface of the sealed...

Embodiment 3

[0046] A preparation method for a medium for separating fungi and yeast-like fungi, comprising the following steps:

[0047] S1, formulation, in parts by weight, take 7 parts of tryptone, 7 parts of animal peptone, 35 parts of glucose, 0.4 part of chloramphenicol and 12 parts of agar and mix evenly, and add 950 parts of purified water to it to prepare a mixed Reagent;

[0048] S2, damp heat sterilization, the mixed reagent is placed in a humid heat environment, and heated at 120°C to 130°C for 30 minutes to perform moist heat sterilization to obtain the sterilized reagent;

[0049] S3, filling, filling the sterilized reagent into the sterilized culture bottle;

[0050] S4, drying and sealing, drying the filled culture bottle, and sealing it with a cap;

[0051] S5, spray code and seal the film, spray the information code on the surface of the culture bottle after plugging and capping, and seal the film;

[0052] S6, labeling, affixing a label on the surface of the sealed cu...

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PUM

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Abstract

The invention relates to the technical field of medical chemiluminescence immunoassay detection, and particularly relates to a culture medium for separating fungi from yeast-like fungi and a preparation method thereof. Casein peptone, animal peptone and glucose are used for providing a proper carbon source and a proper nitrogen source for microorganisms, the ratio of the whole carbon source to thewhole nitrogen source is controllable, meanwhile, the content of the glucose is higher, the pH value of the whole culture medium tends to 5.5-6.5, and growth of fungi and yeast-like fungi is facilitated. Meanwhile, single chloramphenicol is adopted as a bacterial inhibitor to effectively inhibit the growth of bacteria, and to reduce the probability that part of to-be-separated fungi are inhibiteddue to cooperation of multiple bacteriostatic agents. The invention solves the problems that: an existing culture medium for separating fungi is single in carbon source and nitrogen source component,the imbalance of the ratio of a carbon source to a nitrogen source is likely to occur, meanwhile, multiple bacteriostatic agents are combined for bacteriostasis, the bacteriostatic effect on part offungi is overlapped, and the effect of separating part of fungi is poor.

Description

technical field [0001] The invention relates to the technical field of medical chemiluminescence immunoassay detection, in particular to a medium for separating fungi and yeast-like fungi and a preparation method. Background technique [0002] Candida is an opportunistic pathogenic bacteria that exists in the skin, oral cavity, vagina, intestinal mucosa, etc. When the body's immunity is low, it leads to common clinical infections and related diseases. In order to be able to accurately diagnose the type of bacteria at the site of infection, clinically, samples are often collected from the patient’s site for culture, and clinical examiners select suspicious strains for identification based on clinical symptoms, so as to determine the type of bacterial infection at the patient’s site, providing a basis for clinical treatment in accordance with. For the diagnosis of the type of bacteria infected at the patient site, culture is a feasible method in clinical diagnosis at present....

Claims

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Application Information

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IPC IPC(8): C12N1/14C12N1/16C12N1/02C12R1/645
CPCC12N1/14C12N1/16C12N1/02
Inventor 孙月鹏刘正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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