Enterococcus faecium, application thereof, composition and fermentation culture method of enterococcus faecium
A technology of Enterococcus faecium and fermentation medium, applied in the field of microbial fermentation, can solve the problems of large differences in performance of Enterococcus faecium, not necessarily adapting to human or animal intestinal environment, and high cost
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Embodiment 1
[0125] This embodiment provides a method for fermentation and cultivation of Enterococcus faecium HSC-18, wherein the fermentation scale is a 2-ton fermenter.
[0126] 1. Preparation of seed solution
[0127] (1) Seed activation
[0128] Take the Enterococcus faecium HSC-18 stored in the glycerol tube at -80°C. After the Enterococcus faecium HSC-18 glycerol tube is completely melted, draw 0.5mL of the bacterial liquid and inoculate it into 50mL of MRS liquid medium, and place it at 37°C under 160r Cultivate for 12 hours under the condition of 1 / min, then pick the bacterial solution and streak it on the MRS medium plate, place it at 37°C for 18 hours, and obtain a single colony of Enterococcus faecium HSC-18.
[0129] (2) Preparation of primary seed solution
[0130] A single colony of Enterococcus faecium HSC-18 was picked from the MRS medium plate, inoculated in 50 mL of MRS medium, and cultured in a shaker flask at 37°C and 160 r / min for 12 hours to obtain a first-grade se...
Embodiment 2
[0143] This embodiment provides a method for fermentation and cultivation of Enterococcus faecium HSC-18, wherein the fermentation scale is a 30L fermenter. The specific operation process is: according to the method in embodiment 1, prepare the primary seed liquid and the secondary seed liquid, and inoculate the secondary seed liquid into the fermenter of 30L according to the inoculum size of 1% by volume (the liquid capacity is 16L, the fermentation medium is the same as that in Example 1, and the actual elimination method of the fermenter is carried out with reference to Example 1), adjust the temperature of the tank to 37°C and stop stirring and aeration, and after keeping the pressure for 3 hours, Enterococcus faecium HSC-18 enters In the logarithmic growth phase, and the pH drops to 6.0; start stirring and control the rotating speed to 100r / min and micro-ventilation (see obvious bubbles), and add 40% (mass volume percentage, m / V) sodium hydroxide solution to control The p...
Embodiment 3
[0146] This embodiment provides a method for fermentation and cultivation of Enterococcus faecium HSC-18, wherein the fermentation scale is a 2-ton fermenter. Compared with the fermentation culture method of Example 1, the difference of the fermentation culture method of the present embodiment is: the fermentation medium is different, the fermentation medium of the present embodiment includes brown sugar of 10g / L, yeast extract of 12g / L , 10g / L fish peptone, 0.5g / L magnesium sulfate heptahydrate, 1g / L ammonium sulfate, 0.02g / L potassium dihydrogen phosphate, 0.1g / L sodium bicarbonate, 0.3g / L chlorine Potassium chloride and 0.5g / L light calcium carbonate.
[0147] In this example, the fermented liquid in the lower tank was diluted and coated on the MRS medium plate, and three parallel samples were set for each dilution, and counted after standing at 37° C. for 18 hours. Through counting, it can be known that The bacterial count was 8 billion CFU / mL.
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