Novel liquid compound microecological preparation for livestock and poultry and preparation method thereof
A composite micro-ecological and liquid technology, applied in microorganism-based methods, biochemical equipment and methods, microorganisms, etc., can solve the problems of lack of synergistic fermentation mixed strains in liquid fermentation, few types of fermentation accelerators, and bottle expansion, and achieve promotion The effect of synergistic fermentation rate, saving fermentation time, and good synergistic fermentation ability
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Embodiment 1
[0039] Embodiment 1--Isolation and identification of Enterococcus faecalis BD-1
[0040] 1. Isolation, enrichment and purification of Enterococcus faecalis BD-1
[0041] Under aseptic operation conditions, farmers in Xia Village, Zherong County, Ningde City, Fujian Province (coordinates: 119 。 51′59.7″E, 27 。 13′34.0″N) Caecum mucosal segment of self-supporting healthy adult pigs, scrape the mucosal mucus with a sterilized glass slide and put it in the EP tube, dilute it with sterile normal saline for 10 2 Take 0.1mL and spread it on the MRS agar plate containing bromocresol purple indicator (0.01%, g / mL). The colonies that turned yellow were streaked and purified, and the strains that were positive for Gram staining under the microscope and without spores were selected to contain bromocresol purple (0.01%, g / mL), tea polyphenols (0.01%, g / mL) and garlic (0.01%, g / mL) on the MRS agar plate for re-screening, and finally select the colony with obvious yellow color, smooth and...
Embodiment 2
[0075] Embodiment 2--Isolation and identification of Clostridium butyricum RCM-2
[0076] 1. Isolation, enrichment and purification of Clostridium butyricum RCM-2
[0077] Under aseptic operation conditions, farmers in Xia Village, Zherong County, Ningde City, Fujian Province (coordinates: 119 。 52′04.1″E, 27 。 13′32.7″N) The cecal mucosal segment of a healthy adult rooster bred in a closed mountain forest, the mucosal mucus was scraped with a sterilized glass slide and placed in an EP tube, diluted with sterile normal saline for 10 2 Then heated to 60°C for 30min, took 0.1mL and spread it on the RCM agar plate containing bromocresol purple indicator (0.01%, g / mL), after coating, put the RCM agar plate in the anaerobic incubator , cultured at 37°C for 48 hours, selected the colonies that turned yellow in the medium, and purified them by streaking, and selected the rod-shaped strains that were positive for Gram staining and had spores in the microscopic examination, and conta...
Embodiment 3
[0107] Embodiment 3--Enterococcus faecalis BD-1 and Clostridium butyricum RCM-2 co-grow
[0108] (1) Activation of the strain
[0109] Activation of Enterococcus faecalis BD-1: Rinse the slant of Enterococcus faecalis BD-1 with sterile saline in a sterile environment, wash off the bacterial lawn on the surface of the medium, and then inoculate it into MRS liquid medium. 37 ℃ static culture for 48h;
[0110] Activation of Clostridium butyricum RCM-2: Rinse the slant of the test tube of Clostridium butyricum RCM-2 with sterile saline in a sterile environment, wash off the bacterial lawn on the surface of the medium, and then inoculate it into MRS liquid medium medium, 37°C static culture for 48h;
[0111](2) Then inoculate the activation solution of Enterococcus faecalis BD-1, the activation solution of Clostridium butyricum RCM-2, and the combination of the two at a volume ratio of 1:1 in the In the 200 mL anaerobic serum bottle of the MRS liquid medium, the gradient of the ...
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