Efficient fermentation medium and fermentation culture method for enterococcus faecium
A fermentation medium, Enterococcus faecium technology, applied in the direction of microorganism-based methods, biochemical equipment and methods, bacteria, etc., can solve the problems of low fermentation level, high price, increased cost, etc., to achieve high-efficiency fermentation, cost saving, The effect of increasing the amount of viable fermentation bacteria
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Embodiment 1
[0027] This embodiment provides the activation method of Enterococcus faecium E.F-2CCTCC No:M 2018314 strain (preserved in China Center for Type Culture Collection on May 28, 2018, and the preservation place is China. Wuhan. Wuhan University), details as follows:
[0028] Dilute the preserved bacteria powder of Enterococcus faecium with normal saline, mark three zones on the MRS plate medium, and place it in a constant temperature incubator at 37°C for 24 hours; pick a single colony on the plate medium and inoculate it in a container containing 100 mL of liquid MRS Place a 250mL Erlenmeyer flask with liquid culture medium in a constant temperature shaker at 37°C and incubate at 120r / min for 12 hours. Finally, use this bacterial solution to line the third section of the MRS plate medium and cultivate a new single colony for use.
Embodiment 2
[0030] This embodiment provides the growth curve determination method of Enterococcus faecium E.F-2CCTCC No:M 2018314, specifically as follows:
[0031] Pick a single colony of Enterococcus faecium and inoculate it into a 250mL Erlenmeyer flask containing 100mL of liquid MRS medium, place it on a constant temperature shaker at 37°C, and cultivate it at 120r / min for 12h, and then inoculate it with 1% (v / v) inoculum Inoculate into three bottles of 250mL Erlenmeyer flasks containing 150mL MRS liquid medium (30% liquid volume), culture in a constant temperature shaker at 37°C and 120r / min, and measure the bacterial liquid in the Erlenmeyer flasks with a turbidimeter every 2h Turbidity, see Table 1 for turbidity values, draw the growth curve of Enterococcus faecium E.F-2CCTCC No:M 2018314, such as figure 1 shown.
[0032] Table 1 Turbidity value of Enterococcus faecium CCTCC No:M 2018314
[0033]
[0034]
[0035] From Table 1 and attached figure 1 It can be seen that 0-2h...
Embodiment 3
[0037] This example provides the basis for selecting the most suitable carbon source in the culture medium of Enterococcus faecium E.F-2CCTCC No:M 2018314, specifically as follows:
[0038]Using different carbon sources instead of the carbon source in the MRS liquid medium to conduct a single factor test to screen the most suitable carbon source for the growth of Enterococcus faecium. Alternative carbon sources include: glucose, fructose, maltose, sucrose, lactose, soluble starch, corn flour, isomaltose, maltodextrin. The addition amount of different carbon sources was converted and added according to the principle of consistent carbon content in glucose in MRS liquid medium, and MRS liquid medium was set as the control group. The culture medium adjusted the same pH value of the MRS liquid medium, cultured at 120r / min at 37°C for 12h, and then measured the turbidity and the number of viable bacteria of Enterococcus faecium in different carbon source medium, with 10 -5 , 10 -...
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