Bifidobacterium pseudocatenulatum capable of highly utilizing galactooligosaccharide and application of bifidobacterium pseudocatenulatum
A bifidobacterium and viable count technology, applied in the field of microbiology and medicine, can solve the problems of not being able to increase the colonization ability of probiotics, and not being able to enhance the survival or persistence of animal bifidobacteria milk subspecies Bb-12, etc., to achieve Efficient use of galacto-oligosaccharides, increased relative abundance, and fast growth rate
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Embodiment 1
[0072] Example 1: Screening, strain identification and cultivation of Bifidobacterium pseudocatenulatum CCFM1170
[0073] Specific steps are as follows:
[0074] 1. Differential response of pseudosmall chain Bifidobacterium strains in human intestine after galacto-oligosaccharide intervention
[0075] Recruit 10 subjects (1) have not had abdominal or intestinal surgery in the past 1 year (2) have not used antibiotics (except topical drugs) in the past 2 months (3) have not consumed probiotics / prebiotics / synbiotics in the past 1 month Healthy adults who took supplements took 10 grams of galacto-oligosaccharides per day for 4 weeks. Fecal samples were collected at the baseline period before the experiment, 2 weeks of galacto-oligosaccharide intervention, and 4 weeks of galacto-oligosaccharide intervention, and were immediately stored in a -80°C refrigerator until the fecal DNA extraction experiment. One volunteer used antibiotics during the experimental period, one volunteer d...
Embodiment 2
[0091] Embodiment 2: In the YCFA liquid medium of galacto-oligosaccharide as carbon source, the growth characteristics of pseudo small chain bifidobacterium (Bifidobacterium pseudocatenulatum) CCFM1170
[0092] Specific steps are as follows:
[0093] (1) Streak Bifidobacterium pseudospermum CCFM1170, Bifidobacterium pseudospermum CCFM1046, Bifidobacterium pseudoserinus FJSWXJNDX3M3, Bifidobacterium pseudosmallis FJSWXJNDX9M6, Bifidobacterium pseudoserinus FJSWXJNDX16M1 on mMRS solid culture cultured anaerobically at 37°C for 48 hours to obtain a single colony;
[0094] Pick a single colony and inoculate it in MRS liquid medium, culture it at 37°C for 18 hours for activation, and activate for two generations continuously to obtain an activation solution.
[0095] (2) Take 1mL of activation solution in a sterile centrifuge tube, centrifuge at 5000r / min for 15min, discard the upper medium to obtain the sludge, then resuspend the sludge with 1mL of sterile normal saline, and then...
Embodiment 3
[0099] Embodiment 3: the impact of galacto-oligosaccharides on the colonization ability of pseudo small chain Bifidobacterium (Bifidobacterium pseudocatenulatum) CCFM1170
[0100] Specific steps are as follows:
[0101] Pseudomonas bifidobacterium CCFM1170 and the negative control strain Bifidobacterium pseudosquamium CCFM1046 were respectively inserted into mMRS liquid medium and cultured anaerobically at 37°C for 36 hours, then centrifuged at 5000r / min for 15min at 4°C to collect the sludge, After washing with normal saline, resuspend in normal saline, the bacterial concentration is 5×10 9 CFU / mL, the bacterial suspension was obtained, and the bacterial liquid was prepared and used daily. The dose of galacto-oligosaccharides is 0.4 g / day / mouse, which is dissolved in drinking water according to the average daily water intake of the mice, and the drinking water is changed every 5 days.
[0102] 64 SPF grade BALB / c male mice weighing 20-22g were randomly divided into 8 groups...
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