Enterococcus faecalis and application thereof
A technology for Enterococcus faecalis and bacterial agent, which is applied in the field of microorganisms, can solve the problems of short fermentation period, secondary pollution of fermented soybean meal, breeding of miscellaneous bacteria, and unclear background of fermented soybean meal bacteria.
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Embodiment 1
[0041] Example 1. Isolation and Identification of Enterococcus faecalis PF95 CCTCC NO: M 2020852
[0042] 1. Isolation of Enterococcus faecalis PF95
[0043] Accurately weigh 20g of feces samples from weaned healthy piglets from a pig farm in Puyang City, Henan Province, China, put them into a triangular flask filled with 180mL of sterile water, seal it with a parafilm, and shake it in a shaker at 180r / min for 30 minutes , to fully disperse the microorganisms, let it stand for 20 seconds, and then 10 -1 diluent; pipette 100μL 10 -1 Add the diluted solution into a centrifuge tube filled with 900 μL sterile water, and mix well to obtain 10 -2 diluent; pipette 100μL 10 -2 Diluent, add to a centrifuge tube filled with 900 μL sterile water, mix well and serve as 10 -3 Diluent; use the same method to serially dilute to make 10 -4 、10 -5 Wait for a series of dilutions. Take the MRS medium that was sterilized at 121°C for 15 minutes, and use a marker pen to mark 10 -1 、10 -3 ...
Embodiment 2
[0058] Embodiment 2, Enterococcus faecalis (Enterococcus faecalis) PF95 inhibits the characteristics and physiological and biochemical characteristics of ETEC K88
[0059] 1. Determination of the ability of Enterococcus faecalis PF95 to inhibit ETEC K88 The antagonism of Enterococcus faecalis PF95 on ETEC K88 was determined by the agar block diffusion method. After culturing the target bacteria ETEC K88 overnight in Luria-Bertani (LB) liquid medium, take 100uL of the overnight culture, add K88 to the LB agar medium and cool to 50°C, mix well, and pour into the solidified LB agar plate Surface; after solidification, punch a hole in the center of the agar plate with a hole puncher with a diameter of 10.00 mm, and add 200 uL of PF95 bacterial solution cultured for 16 hours. Uninoculated blank MRS broth and penicillin were used as negative and positive controls, respectively. After diffusion at 4°C for 2 hours, the diameter of the inhibition zone was measured, and it was found th...
Embodiment 3
[0085] Embodiment 3, the bile salt resistance of Enterococcus faecalis (Enterococcus faecalis) PF95, simulated gastrointestinal tract and antibacterial spectrum determination
[0086] 1. Determination of Bile Salt Resistance of Enterococcus faecalis PF95
[0087] The seed liquid of the activated Enterococcus faecalis (Enterococcus faecalis) PF95 was mixed evenly with 0.2% bile salt solution in a ratio of 2%, and samples were taken at 0, 1, 2, 3 and 4 hours under room temperature conditions, and each sampling 20 μl was dropped on the MRS plate, incubated at 30°C for 48 hours, and the number of colonies in each sample was determined by the MRS plate colony counting method. The experiment was repeated 3 times, and the results were averaged.
[0088] Table 6. Bile salt tolerance of Enterococcus faecalis PF95
[0089] strain 0 hour bacteria count The number of viable bacteria in 1 hour 2 hours surviving bacteria count 3 hours surviving bacteria 4 hours survivi...
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