Bifidobacterium cect 7765 and use thereof in the prevention and/or treatment of excess weight, obesity and related pathologies
A technology of CECT7765, bifidobacteria, applied in the field of bifidobacteria CECT7765 and its use in the prevention and/or treatment of overweight, obesity and related pathologies, capable of solving problems that cannot be attributed to bifidobacteria, etc.
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Embodiment 1
[0123] Example 1: Isolation and Identification of Pseudostrand Bifidobacterium CECT7765 Strain
[0124] B. pseudostrenobacterium strains were isolated from the feces of healthy breast-fed mice that had not been exposed to bifidobacterium-containing food or treated with antibiotics for at least one month prior to analysis. Samples were stored at 4°C and analyzed in less than two hours after collection. 2 g of samples were dissolved in 10 mM phosphate buffer containing NaCl (PBS) at a concentration of 130 mM, homogenized for 3 min using a Lab-Blender 400 shaker (stomacher) (Seward Medical, London, UK), and diluted in peptone water. Aliquots of 0.1 ml at different decimal dilutions were inoculated on MRS agar containing 0.05% cysteine (Sigma, St. Louis, MO; MRS-C) and 80 μg / ml mupirocin (Man Rogose and Sharpe; Scharlau, Barcelona). After 48 hours of incubation at 37°C under anaerobic conditions (AnaeroGen, Oxoid, UK), isolated colonies were selected and their morphology det...
Embodiment 2
[0130] Example 2: Selection based on ability to modulate macrophage responses involved in low-grade chronic inflammation in vitro Bifidobacterium pseudostrandum CECT7765 strain
[0131] 2.1 Preparation of intestinal bacterial cultures and suspensions
[0132] The strain was inoculated in 10 ml of MRS fermentation broth (Scharlau Chemie S.A., Barcelona, Spain) containing 0.05% of 1% cysteine (MRS-C), cultivated for 24 hours, and then incubated at 37°C under anaerobic conditions (AnaeroGen ; Oxoid, Basingstoke, UK) for 22 hours. Cells were collected by centrifugation (6,000 g, 15 minutes), washed twice with PBS (10 mM sodium phosphate, 130 mM sodium chloride, pH 7.4), and then resuspended in PBS containing 20% glycerol. Aliquots of these suspensions were frozen in liquid nitrogen and stored at -80°C. The number of viable cells after freeze-thaw was determined by culturing on MRSC agar plates for 48 hours. Viability was greater than 90% in all cases. Each aliquot ...
Embodiment 3
[0146] Example 3. Application of pseudostrand-shaped Bifidobacterium CECT7765 strain to the function of immune system cells, Immune and endocrine parameters of peripheral blood and central nervous system, as well as gut Microbiome Combination and inflammatory properties sexual influence
[0147] 3.1 Preparation of the culture of the object strain of the present invention
[0148] The CECT7765 strain was grown in MRS broth (Scharlab, SL-Barcelona, Spain) supplemented with 0.05% (w / v) cysteine, and cultured at 37°C for 22 hours under anaerobic conditions (AnaeroGen; Oxoid, Basingstoke , UK). Cells were harvested by centrifugation (6,000 g, 15 min), washed with phosphate buffered saline (PBS, 10 mM sodium phosphate, 130 mM sodium chloride, pH 7.4), and resuspended in 10% skim milk. Freeze aliquots of the above suspension in liquid nitrogen and store at -80 °C until use. The number of viable cells was determined after 48 hours of incubation on MRS agar plates contain...
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