L.plantarum UA149 strain and application thereof
A technology of Lactobacillus plantarum and UA149, applied in the direction of Lactobacillus, application, bacteria, etc., can solve the problems of liver damage, nervous system adverse reactions, restricted safe use, and many adverse reactions, and achieve hyperuricemia or gout prevention, The effect of reducing the level of thromboxane and alleviating the inflammatory response
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[0028] The preparation method of a kind of bacterial agent of the present invention comprises the following steps:
[0029] Plantarum UA149 strain was expanded to 2L, centrifuged at 6000r / min for 5min, resuspended in normal saline, centrifuged again at 6000r / min for 5min, resuspended in normal saline, washed, centrifuged again at 6000r / min for 5min, collected the sludge, dissolved in In 1L of freeze-drying protectant, freeze-dry to obtain Lactobacillus plantarum UA149 fermentation agent, the number of bacteria is 1.0×10 11 CFU / g.
[0030] Among them, the lyoprotectant is obtained by dissolving 40 g of glucose, 5 g of sodium ascorbate, 80 g of fructooligosaccharide, and 30 g of trehalose in tertiary water, and distilling the volume to 750 mL.
[0031] The Lactobacillus plantarum (L. plantarum) UA149 strain of the present invention can be used in the preparation of products with the function of reducing uric acid or in the preparation of products with the function of anti-gout....
Embodiment 1
[0046] The preparation of embodiment 1 plant Lactobacillus (L.plantarum) UA149 strain
[0047] 1. Isolation of Lactobacillus plantarum strains
[0048] 1. Sample material: succulent leaves.
[0049] Take 5g of succulent plant leaves, add 45mL of normal saline (10-fold dilution) and mix well, take 0.5mL of diluent, and dilute to 10 times with normal saline again. -3 , take 100μL liquid (10 -1 、10 -2 、10 -3 ) were spread on solid LAMVAB medium for cultivation (cultivation temperature 37°C, cultivation time 48-72h). Pick a single colony and inoculate it on a solid MRS medium plate to continue culturing (cultivation temperature 37°C, culture time 48h), and repeatedly streak culture and purify the solid MRS medium plate (cultivation temperature 37°C, culture time 48h), and obtain multiple strains Pure cultured strains.
[0050] 2. Inoculate the multiple strains of purely cultured strains obtained above into liquid MRS medium for culture (culture temperature 37°C, culture time...
Embodiment 2
[0075] Embodiment 2 Plant Lactobacillus (L.plantarum) UA149 strain of the present invention utilizes guanosine and inosine in vitro
[0076] 1. Establishment of HPLC standard curve
[0077] Take a certain amount of solution III, dilute it with solution I 2 times, 3 times, 4 times, 5 times, 6 times, 7 times respectively, shake well and pass through a 0.45 μm microporous membrane. Draw 20 μL each for injection analysis.
[0078] Chromatographic conditions:
[0079] HPLC chromatograph Agilent 1260LC, flow rate 1mL / min, column temperature 30°C, retention time 15min, measurement wavelength 254nm.
[0080] 2. Determination of nucleoside decomposition ability
[0081]The degradation process of guanosine and inosine was detected by high performance liquid chromatography, and the contents of inosine and guanosine were determined simultaneously. Inoculate the activated test strain with 3% inoculum into MRS liquid medium, culture for 17 hours, take 3 mL of culture solution at 4°C, ce...
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