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Pre-enrichment liquid culture medium for repairing cold and thermal injuries of Cronobacter

A technology of damage repair and Cronobacter, which is applied in the direction of microorganism-based methods, bacteria, microorganisms, etc., can solve the problems of poor repair of damaged bacteria, inability of damaged bacteria to grow, physiological and biochemical reactions, epidemic outbreaks, etc., to achieve growth repair good effect

Active Publication Date: 2014-06-18
HEFEI UNIV OF TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Therefore, in the process of food microbiological inspection, the existing pre-enrichment culture medium is not effective in repairing the damaged bacteria or contains selective inhibitors, which leads to the failure of the damaged bacteria to grow or great changes in physiological and biochemical reactions, resulting in Cronobacter in food. False-negative results in bacterial testing led to food contaminated by Cronobacter entering the consumer market. Once these damaged bacteria enter the human body through food, they can be revived under suitable conditions, causing the prevalence of foodborne diseases caused by Cronobacter. outbreak

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0025] for Cronobacter ( Cronobacter ) The pre-enrichment liquid medium for hot and cold damage repair consists of the following substances by weight: peptone 15g, potassium dihydrogen phosphate 1.5g, disodium hydrogen phosphate dodecahydrate (Na 2 HPO 4 12H 2 O) 9.0g, sodium chloride 5g, sucrose 120g, sodium pyruvate 1.0g, magnesium chloride 1.0g, water 1000ml;

[0026] Inoculate 1.0 μL overnight Cronobacter suspension into buffered peptone water (BPW), Enterobacter enrichment broth (EE), tryptone broth (TSB), 37 o C 120rpm shaker cultured for 8 hours, took out the medium, and diluted the medium ten times to measure the total number of colonies. The results showed that the repair medium increased 50 times compared with BPW, and increased 10 times compared with EE and TSB.

Embodiment 2

[0028] for Cronobacter ( Cronobacter ) The pre-enrichment liquid medium for hot and cold damage repair consists of the following substances by weight: peptone 15g, potassium dihydrogen phosphate 1.5g, disodium hydrogen phosphate dodecahydrate (Na 2 HPO 4 12H 2 O) 9.0g, sodium chloride 5g, sucrose 100g, sodium pyruvate 0.8g, magnesium chloride 0.8g, water 1000ml;

[0029] Inoculate 1.0 μL overnight Cronobacter suspension into buffered peptone water (BPW), Enterobacter enrichment broth (EE), tryptone broth (TSB), 37 o C 120rpm shaker cultured for 8 hours, took out the medium, and made ten-fold dilution of the medium to determine the total number of colonies (three repetitions). The results showed that the repair medium increased by 45 times compared with BPW, and increased by 10 times compared with EE and TSB.

Embodiment 3

[0031] for Cronobacter ( Cronobacter ) The pre-enrichment liquid medium for hot and cold damage repair consists of the following substances by weight: peptone 15g, potassium dihydrogen phosphate 1.5g, disodium hydrogen phosphate dodecahydrate (Na 2 HPO 4 12H 2 O) 9g, sodium chloride 5g, sucrose 110g, sodium pyruvate 1.2g, magnesium chloride 1.2g, water 1000ml;

[0032] Inoculate 1.0 μL overnight Cronobacter suspension into buffered peptone water (BPW), Enterobacter enrichment broth (EE), tryptone broth (TSB), 37 o C 120rpm shaker cultured for 8 hours, took out the medium, and diluted the medium tenfold to measure the total number of colonies. The results showed that the repair medium increased 65 times compared with BPW, and increased 10 times compared with EE and TSB.

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PUM

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Abstract

The invention relates to a pre-enrichment liquid culture medium for repairing cold and thermal injuries of Cronobacter. The pre-enrichment liquid culture medium comprises peptone, monopotassium phosphate, disodium hydrogen phosphate, sodium chloride, sucrose, sodium pyruvate, magnesium chloride and water. By verifying a repairing effect of the culture medium by virtue of a lot of food-borne pathogenic bacteria, results show that compared with existing pre-enrichment culture media such as BPW (Buffered Peptone Water), EE (Enterobacteria Enrichment Broth), TSB (Trypticase Soy Broth) and the like, the growth effect and repairing effects of physiological and biochemical indexes of the pre-enrichment liquid culture medium are greatly improved, the missing inspection defect of the Cronobacter in food inspection quarantine processes can be overcome, the detection ratio of the Cronobacter can be improved, and the growth and propagation of non-target bacteria such as salmonella and the like can be effectively restrained. The pre-enrichment liquid culture medium is suitable for rapidly repairing the Cronobacter in various foods and has important significances in the prevention and control of the occurrence and propagation of food-borne diseases caused by the food-borne Cronobacter infection.

Description

technical field [0001] The invention belongs to the technical field of food microbiological inspection, and in particular relates to a liquid culture medium for enriching Cronobacter before cold and heat damage repair. Background technique [0002] Cronobacter ( Cronobacter ), is an important food-borne pathogenic bacterium, a gram-negative bacillus belonging to the family Enterobacteriaceae, which can cause meningitis, fatal colitis, and bacteremia in newborn infants. Epidemiological data surveys show that infant formula Milk powder is the main medium of its infection. [0003] During food processing, through high heat, low cold, drying, sterilization and other processing units, it is easy to cause damage to Cronobacter. Therefore, in the process of food microbiological inspection, the existing pre-enrichment culture medium is not effective in repairing the damaged bacteria or contains selective inhibitors, which leads to the failure of the damaged bacteria to grow or gre...

Claims

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Application Information

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IPC IPC(8): C12N1/20C12R1/01
Inventor 叶应旺李辉凌娜韩永佳
Owner HEFEI UNIV OF TECH
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