High-density fermentation medium for enterococcus faecalis for feed and fermentation method of medium
A technology of high-density fermentation and Enterococcus faecalis, which is applied in the direction of microorganism-based methods, biochemical equipment and methods, bacteria, etc., can solve the difficulties of Enterococcus faecalis in achieving high-density fermentation, lack of nutrients, and difficulty in achieving high-density fermentation, etc. Problems, achieve the effect of shortening the production cycle, improving production efficiency and reducing separation costs
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Embodiment 1
[0026] Example 1 Preparation of fermentation medium and comparison of fermentation
[0027] 1. The components and contents of Enterococcus faecalis high-density fermentation medium are:
[0028] Sucrose 20g / L, peptone 10g / L, yeast powder 10g / L, K 2 HPO 4 2g / L, sodium citrate 2g / L, MgSO4: 0.2g / L, FeSO4: 0.1g / L, MnSO4: 55mg / L.
[0029] 2. Medium preparation method:
[0030] (1) Weigh each component according to the above content and dissolve it with distilled water, in which sucrose is dissolved separately;
[0031] (2) Sucrose was sterilized separately at 115°C for 20 minutes, and the other components were put into the fermentation tank at 121°C and sterilized for 30 minutes;
[0032] (3) Before inoculation, add sucrose to the fermentor through aseptic operation, stir and mix well, and get it.
[0033] 3 Comparison of high-density fermentation and existing technology fermentation
[0034] (1) Activate the frozen Enterococcus faecalis on the MRS agar plate three times, pick a single colony ...
Embodiment 2
[0049] Example 2 Preparation of fermentation medium and comparison of fermentation
[0050] 1. The components and contents of Enterococcus faecalis high-density fermentation medium are:
[0051] Sucrose 20g / L, peptone 15g / L, yeast powder 15g / L, K 2 HPO 4 3g / L, sodium citrate 4g / L, MgSO4: 0.2g / L, FeSO4: 0.1g / L, MnSO4: 80mg / L.
[0052] 2. Medium preparation method:
[0053] (1) Weigh each component according to the above content and dissolve it with distilled water, in which sucrose is dissolved separately;
[0054] (2) Sucrose was sterilized separately at 115°C for 20 minutes, and the other components were put into the fermentation tank at 121°C and sterilized for 30 minutes;
[0055] (3) Before inoculation, add sucrose to the fermentor through aseptic operation, stir and mix well, and get it.
[0056] 3 Comparison of high-density fermentation and existing technology fermentation
[0057] (1) Activate the frozen Enterococcus faecalis on the MRS agar plate three times, pick a single colony ...
Embodiment 3
[0072] Example 3 Preparation of fermentation medium and comparison of fermentation
[0073] 1. The components and contents of Enterococcus faecalis high-density fermentation medium are:
[0074] Sucrose 30g / L, peptone 15g / L, yeast powder 25g / L, K 2 HPO 4 2g / L, sodium citrate 4g / L, MgSO4: 0.2g / L, FeSO4: 0.1g / L, MnSO4: 60mg / L.
[0075] 2. Medium preparation method:
[0076] (1) Weigh each component according to the above content and dissolve it with distilled water, in which sucrose is dissolved separately;
[0077] (2) Sucrose was sterilized separately at 115°C for 20 minutes, and the other components were put into the fermentation tank at 121°C and sterilized for 30 minutes;
[0078] (3) Before inoculation, add sucrose to the fermentor through aseptic operation, stir and mix well, and get it.
[0079] 3 Comparison of high-density fermentation and existing technology fermentation
[0080] (1) Activate the frozen Enterococcus faecalis on the MRS agar plate three times, pick a single colony a...
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