Inoculant, feed or additive and removal method for mycotoxins
A technology of mycotoxins and additives, applied in the field of microorganisms, can solve the problems of decreased removal efficiency, less research, and difficulty in achieving efficient removal
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[0038] The present invention also includes the preparation method of the bacterial agent, wherein, the method comprises respectively inoculating at least two of the above-mentioned molds, yeasts and bacteria in the corresponding medium for cultivation, and then inoculating the obtained The culture is preferably compounded according to the above proportions to obtain the microbial agent of the present invention.
[0039] In the present invention, the method of inoculating the mold, yeast and bacteria in the culture medium can be changed in a wide range, for example, the method can include: respectively cultivating the mold, yeast and bacteria in separate culture systems Bacteria; and the respectively cultured mold, yeast and bacteria are mixed in proportion to obtain the microbial inoculant.
[0040] In the second aspect, the present invention also provides the application of the above bacterial agent in removing mycotoxins.
[0041] According to the present invention, the myc...
preparation example
[0067] Inoculate mold spores and yeast in PDA medium with 1% inoculum respectively, and cultivate them at 37°C for a period of time to make the concentration of mold spores 10 9 CFU / ml, the concentration of yeast is 10 9 CFU / ml. Bacteria were inoculated in LB medium with an inoculum of 1%, cultured at 37°C, and the culture time was such that the concentration of bacteria was 10 9 CFU / ml.
[0068] The bacterium liquid after cultivating is carried out the preparation of composite bacterial agent according to the proportioning of each embodiment in the following table 1, and in the final bacterial agent, the total number of viable bacteria contained in each gram of the bacterial agent is 10 9 CFU.
[0069] Table 1
[0070]
[0071]
Embodiment 1-7
[0073] Used to illustrate the removal of bacterial agents provided by the invention to mycotoxins
[0074] Carry out the preparation of bacterial agent according to the proportioning of each embodiment in Table 1, then respectively add 0.5ppm ochratoxin A, 0.5ppm fumonisin and 0.5ppm T2 toxin in the prepared bacterial agent, after adding, in 37 ℃, After reacting for 2 hours under the condition of pH value 7, 20 μL of the treated sample was taken into high performance liquid chromatography to detect the residues of each toxin, and the removal rate was calculated. The results are shown in Table 2.
[0075] Wherein, toxin removal rate=(toxin initial concentration-toxin concentration after treatment) / toxin initial concentration×100%.
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