Check patentability & draft patents in minutes with Patsnap Eureka AI!

Selective chromogenic culture medium of listeria monocytogenes and preparation method of selective chromogenic culture medium

A technology of Listeria monocytogenes and chromogenic medium is applied in the field of preparation of selective chromogenic medium, which can solve the problems of prone to false negative and false positive results, time-consuming, affecting clinical diagnosis and treatment, etc. Single-strength Listeria monocytogenes is difficult to isolate, culture and identify, and the effect of low cost

Inactive Publication Date: 2015-03-04
SOOCHOW KH BIO SCI & TECH CO LTD KHB
View PDF0 Cites 5 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, to date no assay has met all the criteria listed above
The traditional method is time-consuming, heavy workload, and does not meet the current needs of rapid and sensitive detection of microorganisms
Compared with the traditional method, the molecular biology detection method greatly reduces the workload, but the positive samples detected should be compared with the traditional method, and the detection is prone to false negative and false positive results
[0004] At present, the selective medium used for the isolation of Listeria monocytogenes, including the chromogenic medium, can only selectively cultivate the Listeria group but cannot selectively cultivate the Listeria monocytogenes, and Listeria monocytogenes other than Listeria monocytogenes The genus is non-pathogenic or only pathogenic to animals. The microbiological identification of Listeria monocytogenes requires complex biochemical reaction tests, and the time required for identification is too long, which affects clinical diagnosis and treatment.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Selective chromogenic culture medium of listeria monocytogenes and preparation method of selective chromogenic culture medium
  • Selective chromogenic culture medium of listeria monocytogenes and preparation method of selective chromogenic culture medium
  • Selective chromogenic culture medium of listeria monocytogenes and preparation method of selective chromogenic culture medium

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0020] Listeria monocytogenes selective chromogenic medium, wherein each 1000mL medium contains the following components by weight: heart-brain extract 5g, agar 2g, peptone 2g, 5-bromo-4-chloro-3-indole- Inositol-1-phosphate potassium 0.1g, dimethylformamide 0.05g, magnesium sulfate 0.2g, lithium chloride 0.2g, potassium pyruvate 0.3g, 3-morpholinopropane-1-sulfonic acid 0.2g, Cycloheximide 0.015g, the balance is water.

[0021] The specific preparation method is as follows:

[0022] 1) dissolving the specific enzyme chromogenic substrate in dimethylformamide to form a mixed solution;

[0023] 2) Heart-brain extract, agar, peptone, magnesium sulfate, lithium chloride, oxygen scavenger, 3-morpholinopropane-1-sulfonic acid, and bacteria inhibitors are mixed in proportion;

[0024] 3) Add the mixed solution of step 1) into the mixed solution of step 2), and add water to form a solution with a certain concentration;

[0025] 4) Sterilize at 120°C for 15 minutes and cool down fo...

Embodiment 2

[0027] Listeria monocytogenes selective chromogenic medium, wherein each 1000mL medium contains the following components by weight: heart-brain extract 20g, agar 6g, peptone 5g, 5-bromo-4-chloro-3-indole- Inositol-1-phosphate potassium 1g, dimethylformamide 20g, magnesium sulfate 0.5g, lithium chloride 0.5g, cysteine ​​0.6g, 3-morpholinopropane-1-sulfonic acid 1.0g, acridine hydrochloride Pyridine yellow 15g, balance is water.

[0028] The specific preparation method is as follows:

[0029] 1) dissolving the specific enzyme chromogenic substrate in dimethylformamide to form a mixed solution;

[0030] 2) Heart-brain extract, agar, peptone, magnesium sulfate, lithium chloride, oxygen scavenger, 3-morpholinopropane-1-sulfonic acid, and bacteria inhibitors are mixed in proportion;

[0031] 3) Add the mixed solution of step 1) into the mixed solution of step 2), and add water to form a solution with a certain concentration;

[0032] 4) Sterilize at 120°C for 15 minutes and cool ...

Embodiment 3

[0034] Listeria monocytogenes selective chromogenic medium, in which every 1000mL medium contains the following components by weight: heart-brain extract 12g, agar 5g, peptone 3g, 5-bromo-4-chloro-3-indole- Inositol-1-phosphate potassium 0.6g, dimethylformamide 0.2g, magnesium sulfate 0.3g, lithium chloride 0.4g, sodium thioglycolate 0.5g, 3-morpholinopropane-1-sulfonic acid 0.8g, naphthalene 0.02 parts of picroic acid, 0.05 parts of cycloheximide, 7 parts of acriflavine hydrochloride, and the balance is water.

[0035] The specific preparation method is as follows:

[0036] 1) dissolving the specific enzyme chromogenic substrate in dimethylformamide to form a mixed solution;

[0037] 2) Heart-brain extract, agar, peptone, magnesium sulfate, lithium chloride, oxygen scavenger, 3-morpholinopropane-1-sulfonic acid, and bacteria inhibitors are mixed in proportion;

[0038] 3) Add the mixed solution of step 1) into the mixed solution of step 2), and add water to form a solution ...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention provides a selective chromogenic culture medium of listeria monocytogenes. Every 1000ml of the culture medium comprises the following components by weight: 5-20g of heart-brain extract, 2-6g of agar, 2-5g of peptone, 0.1-1g of a specific enzyme chromogenic substrate, 0.05-20g of dimethylformamide, 0.2-0.5g of magnesium sulfate, 0.2-0.5g of lithium chloride, 0.3-0.6g of an oxygen scavenger, 0.2-1.0g of 3-morpholino-propane-1-sulfonic acid, 6-17g of a bacteria inhibitor and the balance being water; the specific enzyme chromogenic substrate is 5-bromo-4-chloro-3-indolyl-inositol-1-phosphate. A listeria monocytogene specific chromogenic substrate is made into the selective chromogenic culture medium, so that the specific selection and chromogenic functions of listeria monocytogenes are realized at low cost, and the problem that the listeria monocytogenes are difficult to isolate, culture and identify is solved.

Description

technical field [0001] The invention relates to a selective chromogenic medium suitable for Listeria monocytogenes and a preparation method of the selective chromogenic medium. Background technique [0002] Listeria was first isolated from rabbits and guinea pigs in the United Kingdom in 1926, and its pathogenicity to humans was confirmed in 1929. There are 6 species of the bacterium, Listeria monocytogenes (referred to as Listeria monocytogenes, LM), Listeria innocua, Listeria sierra, Listeria welis, Listeria ovis bacterium and Listeria gravidarum. Among them, Listeria monocytogenes is pathogenic to humans and animals, Listeria ovis is pathogenic to animals, and the rest are non-pathogenic. Listeria monocytogenes is ubiquitous in soil, animals, and aquatic products. The foods most involved are soft cheeses, dairy products, sausages, smoked fish, lettuce foods, deli foods, and frozen ready-to-eat foods. Because of its unique physiological characteristics, it can cause hum...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
IPC IPC(8): C12Q1/04
Inventor 金京勋
Owner SOOCHOW KH BIO SCI & TECH CO LTD KHB
Features
  • R&D
  • Intellectual Property
  • Life Sciences
  • Materials
  • Tech Scout
Why Patsnap Eureka
  • Unparalleled Data Quality
  • Higher Quality Content
  • 60% Fewer Hallucinations
Social media
Patsnap Eureka Blog
Learn More