Bifidobacterium longum SQS7-31, as well as preparation method and application thereof
A technology of Bifidobacterium longum and Bifidobacterium, applied in the biological field, can solve the problem of reduced survival rate and achieve the effect of excellent tolerance and superior survival rate
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Embodiment 1
[0032] Embodiment 1: Separation and purification of bacterial strains
[0033] Take 5 grams of fresh infant feces and shake it with 50ml of feces diluent to make a homogenate, put 1ml of the feces homogenate into a test tube with 9ml of MRSC medium, adjust the pH value to 3.0, culture it anaerobically at 37°C for 24 hours, and then pick it up with an inoculation loop The bacterial solution was streaked on the MRSC solid medium plate, and cultured anaerobically at 37°C for 24h. Under sterile conditions, use an inoculation loop to pick colonies on the streaked MRSC solid medium plate, continue to streak on a new MRSC plate, place the plate in an anaerobic box, and culture it in a 37°C incubator for 72 hours. A single colony was picked for microscopic examination to confirm that the pure strain was isolated. The strain was identified as Bifidobacterium longum and named as Bifidobacterium longum SQS7-31.
Embodiment 2
[0034] Embodiment 2: Microscopic examination of bacterial strain
[0035] Under sterile conditions, inoculate Bifidobacterium longum SQS7-31 with rings, smear on glass slides, prepare slides and Gram stain, and observe the morphology of bacteria under a microscope.
Embodiment 3
[0036] Embodiment 3: strain fermentation
[0037] Use an inoculation loop to pick two rings of Bifidobacterium longum SQS7-31 from the MRSC slant, put them into a test tube containing 10ml MRSC liquid medium, and after culturing for 24 hours, insert SQS7-31 into MRSC liquid culture with 1% inoculum Medium, 37 ° C anaerobic culture for 24 hours, the Bifidobacterium longum SQS7-31 fermentation broth was obtained.
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