Lactobacillus plantarum BUFX and application thereof in metabolic syndrome
A technology of Lactobacillus plantarum and metabolic syndrome, applied in the field of microbiology and its application, can solve problems such as differences in the influence of intestinal flora, complex pathogenesis of diabetes, etc., achieve excellent hypoglycemic ability, improve glucose tolerance and insulin resistance, reduce Effects of Body Weight and Lipid Levels
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0042] Example 1: Sample collection and strain isolation
[0043] The feces of healthy adults living in the urban area of Beijing for a long time were collected as screening samples. The collected subjects had never taken antibiotics, probiotics, or gastrointestinal diseases before collection. Dilute the collected feces samples and spread them on YCFA medium, culture them anaerobically at 37°C for 24-48 hours, and separate and obtain different single colonies on the plate. Pick different single colonies with a sterilized inoculation loop, streak and purify them on a new YCFA solid medium plate, culture anaerobically at 37°C for 48 hours, and obtain 29 purified colonies, which are marked as L1-L29 respectively.
[0044] It should be noted that the dilution of the stool sample is a conventional method in the art, and the present invention is not limited. In one embodiment of the present invention, the stool sample is diluted with clean water.
Embodiment 2
[0045] Embodiment 2: preparation of living bacteria liquid, metabolites and inactivated bacteria
[0046] 2.1 Culture of bacteria
[0047] Take -80°C frozen bacteria liquid and spread it on the YCFA solid plate, and after inverting culture at 37°C for 24-48 hours, take a single colony and inoculate it in the liquid YCFA medium, and cultivate it at 37°C for 18-24 hours to obtain the first-generation bacterial liquid; Take 10% of the first-generation bacterial solution and inoculate it into fresh YCFA liquid medium, incubate at 37°C for 18-24 hours to obtain the second-generation bacterial solution; take 10% of the second-generation bacterial solution and inoculate it into fresh YCFA liquid medium, and incubate at 37°C for 18-24 hours to obtain working bacteria.
[0048] Obtaining live bacteria
[0049] In an embodiment of the present invention, the working bacterial solution obtained in step 1 was placed at 13,000 rpm and centrifuged at 4°C for 15 minutes, the supernatant was...
Embodiment 3
[0055] Embodiment 3: have the bacterial strain screening and the identification that promotes cell glucose cell effect
[0056] 3.1 Strain identification
[0057] Streak culture the isolated single colony, then pick a single colony and spread it on the mass spectrometer plate, add the lysate and matrix to dry, and then use the MALDI-TOF MS 1000 mass spectrometer (Autobio) to identify each strain. information.
[0058] Cellular glucose consumption assay
[0059] The human liver cancer HepG2 cells used in the present invention were purchased from the National Biomedical Laboratory Cell Resource Bank. The cell culture adopts a culture method known in the art, which is not limited in the present invention.
[0060] Human liver cancer HepG2 cells were cultured at 37°C and 5% CO 2 In high glucose DMEM medium containing 10% fetal bovine serum (FBS) under the condition, double antibodies (100 µg / ml penicillin and 100 µg / ml streptomycin) were added to the medium at a ratio of 1:100...
PUM
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