Screening and application of fish-derived enterococcus faecium R8
A technology for separation and screening of Enterococcus faecium, applied in the fields of application, bacteria, antibacterial drugs, etc., can solve the problems of inability to colonize and unstable of probiotic strains, reduce the impact of pollution and human health, improve the survival rate and increase the growth rate. The effect of reducing the incidence of bacterial drug resistance
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0026] Example 1: Isolation and identification of probiotic strains
[0027] 1. Isolation of strains
[0028] The samples were taken from healthy crucian carp purchased in the market. After the body surface was sterilized with 75% medical alcohol, the crucian carp was aseptically dissected and the intestines were taken out, and pre-cooled sterilized saline was added at a ratio of 1:10. Homogenate, the homogenate is serially diluted by 10 times, spread on the MRS medium plate, and observe after 24-36 hours of constant temperature cultivation at 37°C. Select colonies with clear edges, scattered and about 1 mm in size for pure culture. The pure cultures were preliminarily judged by morphological observation and Gram staining, and the Gram-positive cocci in single, paired or chained form were passaged and preserved. The growth characteristic of the bacterial strain of this invention on MRS agar culture sees figure 1 , see Gram staining properties figure 2 .
[0029] The stra...
Embodiment 2
[0046]Embodiment 2: the antibacterial test of Enterococcus faecium bacterial strain R8
[0047] Aeromonas vernerii, Staphylococcus hemolyticus, Vibrio parahaemolyticus and Vibrio vulnificus (provided by Aquatic Animal Disease and Immunology Laboratory, Fisheries College, Tianjin Agricultural University) were used as indicator bacteria. Adopt spot method (Smith P, 1993) primary screening, the method of Oxford cup method (Liu Dongmei, 2006) secondary screening to carry out bacteriostasis test, concrete steps are as follows: adjust indicator bacteria liquid concentration to be 10 6 cfu / mL, draw 0.1mL and spread it on the LB agar medium, then pick a single strain to be tested with the inoculation loop and spot it on the plate. Incubate at 37°C for 24 hours and observe the inhibition zone.
[0048] The Oxford cup method was used for re-sieving. Adjust the concentration of the strain to be tested after 24h of activation to 10 7 cfu / mL, adjust the concentration of indicator bacter...
Embodiment 3
[0052] Example 3: Safety evaluation of Enterococcus faecium strains
[0053] 1. Hemolysis test
[0054] Spot the R8 bacterial solution after 24 hours of cultivation on the rabbit blood plate, incubate at 37°C for 24 hours, and judge the production of hemolysin according to the formation of transparent circles around the colonies. As a result, there was no transparent circle and no hemolytic reaction.
[0055] 2. Animal tests
[0056] The R8a strain was inoculated on LB agar medium, cultured at 37°C for 24 hours, and then eluted with 0.75% sterile saline to obtain a bacterial suspension. The bacterial suspension was serially diluted 10 times, and the bacterial suspension of different dilutions was used aseptic Inject 0.1 mL of each crucian carp intraperitoneally with a syringe, and the concentration of the bacteria solution is 1.0×10 8 cfu / mL, 12 tails were injected into each group as the test group. The same volume of sterile saline was injected as the control group. Put ...
PUM
Property | Measurement | Unit |
---|---|---|
diameter | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com