Lactobacillus gasseri and application thereof for preparing vaginal bacteriostatic drugs
A technology of Lactobacillus gasseri and drugs, applied in the field of microorganisms, can solve the problems of not having the ability to inhibit vaginal pathogenic bacteria, and achieve the effect of superior vaginal epithelial cell adhesion, active and stable biological characteristics, and inhibition of Candida albicans
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Embodiment 1
[0054] Embodiment 1 (isolation and inoculation, purification, enrichment culture of Lactobacillus gasseri RD-0046 flora)
[0055] 1. Isolation and inoculation of Lactobacillus gasseri RD-0046 flora: Use two sterile cotton swabs to collect the secretions on the side wall of the subject's vagina, and inoculate them with different concentrations within 24 hours in the prepared MRS Petri dish of culture medium, and label the information, place the Petri dish in an anaerobic tank, and put CO 2 Put the gas-producing bag in a 37°C incubator and incubate for more than 48 hours.
[0056] 2. Purification and enrichment culture of Lactobacillus gasseri strain RD-0046: Count the colonies according to their different shapes (surface, edge, etc.) and size, and count the ones with the same shape and size as one, and pick out a single colony from the inoculation loop. A few bacteria were inoculated into the MRS solid medium according to the "slash method" to obtain isolated and purified sing...
Embodiment 2
[0057] Embodiment 2 (identification and preservation of Lactobacillus gasseri RD-0046 bacterial strain)
[0058] 1. Culture characteristics, staining microscopic examination and morphological characteristics: the colonies obtained after culture are as attached figure 1 , the colony is round, with neat edges, smooth surface, relatively flat, and translucent; the smear of the pure culture of the bacteria was taken for Gram staining, and the results are shown in the attached figure 2 , Gram staining was positive, thin rod-shaped, blunt-rounded end, arranged in chains or filaments, the results showed that the isolated strain was preliminarily determined to be Lactobacillus.
[0059] 2. Identification of 16SrDNA gene sequence: DNA was extracted with a bacterial genomic DNA extraction kit, and primers 27F (5'-AGAGTTTGATCMTGGCTCAG-3') and 1492R (5'-TACGGYTACCTTGTTACGACTT-3') were used for PCR amplification. The PCR product was subjected to gel electrophoresis to determine the 16S r...
Embodiment 3
[0072] Embodiment 3 (determination of metabolites of Lactobacillus gasseri RD-0046)
[0073] 1. Determination of lactic acid content in the metabolites of Lactobacillus gasseri RD-0046: adopt high performance liquid phase method (0.005M sulfuric acid aqueous solution (0.28ml sulfuric acid (98%)-1000ml water, pH is about 2.1) to cultivate this bacterial strain for 24-48h to ferment The lactic acid of liquid is detected, and the result indicates that lactic acid (L / D lactic acid sum) is about 35mg / mL, which is much higher than the lactic acid content of commercially available Lactobacillus delbrueckii (about 15mg / mL) and conventional Lactobacillus gasseri. Lactic acid detection map see attached Figure 4
[0074] 2. Determination of hydrogen peroxide content in the metabolites of Lactobacillus gasseri RD-0046: semi-quantitative determination of hydrogen peroxide was carried out according to the peroxidase method of Mcgroarty et al., and the isolated and identified Lactobacillus...
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