Lactobacillus plantarum with weight reducing function and application thereof
A technology of Lactobacillus plantarum and function, applied in the field of microorganisms, can solve the problems of obvious differences in individual intestinal flora and physiological state, and achieve the effects of reducing fat accumulation, inhibiting fat synthesis, and lowering blood lipids
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Embodiment 1
[0042] The bacterial strain provided by the present invention is identified as belonging to Lactobacillus plantarum (Lactobacillus plantarum), named 1701, and was preserved in the General Microorganism Culture Collection Center of China Microbiology Culture Collection Management Committee on October 23, 2019, and the microorganism preservation number is CGMCC NO. 18728.
[0043] The bacterial strain provided by the present invention is isolated by the inventor from yogurt powder sample collected in the village of Shigatse City, Tibet Autonomous Region of my country.
[0044] The biological properties of bacterial strain Lactobacillus plantarum 1701 of the present invention are as follows:
[0045] Morphological characteristics: In MRS agar medium, the growth form is milky white, opaque, round, smooth and moist surface, neat edges, and centrally raised colonies. Gram staining was typically positive, and the cells were observed under a microscope to be long rod-shaped, without ...
Embodiment 2
[0053] Lactobacillus plantarum 1701 of the present invention, reference commercial bacterial strain Lactobacillus rhamnosus GG (LGG) and Lactobacillus casei Daita strain (LcS) after second-generation activation, get the bacterial liquid at the end of logarithmic growth, centrifuge at 4000rpm for 10min, discard the supernatant, To obtain the bacteria sludge, perform the following operations respectively: ①Add the same volume of MRS solution with pH 2.5, blow and mix well, incubate at 37°C, and measure the number of bacteria after incubation for 0h, 1h, 2h, and 4h by the dilution coating counting method Change; ② Add the same volume of MRS solution containing 0.3% bile salts, pipette and mix well, incubate at 37°C, and measure the changes in the number of bacteria after incubation for 0h, 4h, and 8h by the dilution coating counting method. Strain survival rate calculation formula:
[0054] Strain survival rate (%)=N1 / N0×100%.
[0055] N1 is the number of viable bacteria after t...
Embodiment 3
[0061] The HT-29 cell culture system was established, and the cells were grown in DMEM medium containing 10% fetal bovine serum (containing penicillin 100 U / mL, streptomycin 100 mg / mL). After the cells were transferred to the third passage, they were digested with 0.25% trypsin (containing EDTA) to obtain a single cell suspension, and the cells were divided into 1×10 6 The density of cells / well was seeded in a 12-well cell culture plate with cell slides placed, at 37°C, 5% CO 2 Cultured in the incubator for 2 days.
[0062] After the bacterial strain Lactobacillus plantarum 1701 of the present invention, the contrast commercial bacterial strain Lactobacillus rhamnosus GG (LGG) and Lactobacillus casei Daita strain (LcS) are activated by the second generation, take the bacterial liquid at the end of logarithmic growth, centrifuge at 4000rpm for 10min, discard the supernatant , to obtain the bacteria sludge, resuspended in DMEM complete medium containing 10% fetal bovine serum (...
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