Enterococcus faecium GXSCU1 capable of efficiently degrading vomitoxin, microbial agent as well as preparation method and application of microbial agent
A technology of microbial agent and deoxynivalenol, which is applied in the field of microbiology, can solve the problem that Enterococcus faecium degrades deoxynivalenol and other problems that have not been found, and achieve the effect of eliminating harm
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[0044] The present invention also provides a preparation method of the above-mentioned microbial inoculum, inoculating the Enterococcus faecium GXSCU1 into a culture medium and culturing to obtain the microbial inoculum.
[0045] Unless otherwise specified, the present invention has no special requirements on the source of each component in the medium, and commercially available products well known to those skilled in the art can be used.
[0046] The culture medium of the present invention includes 0.5-4wt.% of glucose, preferably 1-3wt.%, more preferably 2wt.%.
[0047] The culture medium of the present invention includes 0.5-3 wt.% of peptone, preferably 0.8-1.5 wt.%, more preferably 1 wt.%.
[0048] The culture medium of the present invention includes 0.1-2wt.% of yeast powder, preferably 0.3-1wt.%, more preferably 0.5wt.%.
[0049] The culture medium of the present invention includes 0.5-3wt.% of sodium chloride, preferably 0.8-1.5wt.%, more preferably 1wt.%.
[0050] T...
Embodiment 1
[0062] The strain was isolated from a milk sample from a dairy farm in Guangxi. Draw 100 μL of milk sample in the ultra-clean workbench, add it to 900 μL of sterile water for dilution, and dilute to 10 -4 、10 -5 That's it. Then draw 100μL on the plate (media formula: 2% glucose, 1% peptone, 0.5% yeast powder, 1% sodium chloride, 0.2% potassium dihydrogen phosphate, 0.1% dipotassium hydrogen phosphate, 3% agar and 92.2% water) for coating, and after the culture medium was absorbed, the plate was inverted, and placed in an incubator at a culture temperature of 35°C for 24 hours. After 24 hours, pick round, small, raised, smooth, and white colonies for streak culture, and then pick round, small, raised, smooth, white single colonies Save for backup.
[0063] 1. Identification of colony morphology
[0064] The screened GXSCU1 bacterial strain was inoculated on the petri dish by streaking on the plate (the medium on the petri dish was composed of the following components in ma...
Embodiment 2
[0076] A microbial inoculum for degrading vomitoxin, the preparation method of the microbial inoculum is as follows:
[0077] 1) The GXSCU1 bacterial strain screened in Example 1 is activated by streaking on a plate, and its activation medium is composed of the following components in mass percentage: 2% glucose, 1% peptone, 0.5% yeast powder, 1% chlorinated Sodium, 0.2% potassium dihydrogen phosphate, 0.1% dipotassium hydrogen phosphate, 3% agar and 92.2% water; the pH value of the activation medium is 6.0, the temperature of the activation culture is 34-36°C, and the time of the activation culture is 24h ;
[0078] 2) Propagation and large-scale production of bacterial strains: its propagation medium is composed of the following components in mass percentage: 2% glucose, 1% peptone, 0.5% yeast powder, 1% sodium chloride, 0.2% diphosphate Potassium hydrogen phosphate, 0.1% dipotassium hydrogen phosphate and 95.2% water; the pH value of the propagation medium is 6.0, and the ...
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