Microorganism composite bacterial preparation, and preparation method and applications thereof
A compound bacterial agent and microorganism technology, applied in the field of environmental microorganisms, can solve the problems of low removal efficiency, incomplete degradation of aromatic hydrocarbons, poor environmental adaptability and functional stability, etc., achieving good stability and breaking industry technical barriers and equipment requirements. brief effect
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[0042] The preparation method of the above-mentioned microbial composite bacterial agent will be further described below, and the preparation method of the microbial composite bacterial agent comprises:
[0043] S1, the first activation culture
[0044] Specifically, the first activation culture is to inoculate Dieselophane, Pseudomonas spongiosa, Acinetobacter venezius and M. venezii into the liquid culture medium (liquid HLB) of the activated strains for cultivation, that is, -70°C The preserved glycerol tube strains of the above four strains were respectively inoculated into 15mL culture tubes containing 2-5mL activated strain liquid medium, and the culture tubes were placed in a shaking shaker at 20-28°C and 180-220r / min Incubate for 48-120 hours.
[0045] Wherein, the activated strain liquid medium includes tryptone 8-12g / L, yeast extract 4-6g / L, sodium chloride 25-35g / L and deionized water; the pH value is 6-7.5.
[0046] S2, the second activation culture
[0047] The...
Embodiment 1
[0062] Firstly, Dieselophane with the preservation registration number 1A00001, Pseudomonas spongiosa with the preservation registration number 1A00102 and the preservation registration number 1A00294 obtained from the China Marine Microorganism Culture Collection Management Center (MCCC) were stored at -70°C. The glycerol tube strains of Acinetobacter venezius and Marinococcus dehydrocarbons with deposit registration number 1A03971 were respectively inoculated into 15mL culture tubes containing 5mL liquid HLB, and the culture tubes were placed on a shaking shaker at 28°C and 220r / min. cultured for 120 hours. Then, the obtained bacterial liquid was streaked in the solid medium of the activated strain and placed in a constant temperature incubator at 28°C for rejuvenation for 96 hours, and the colonies on the plate were each inoculated into 15mL culture tubes containing 5mL of liquid HLB and placed at 28°C. Incubate overnight in a shaking shaker at 200r / min.
[0063] Secondly,...
Embodiment 2
[0067] Firstly, Dieselophane with the preservation registration number 1A00001, Pseudomonas spongiosa with the preservation registration number 1A00102 and the preservation registration number 1A00294 obtained from the China Marine Microorganism Culture Collection Management Center (MCCC) were stored at -70°C. The glycerol tube strains of Acinetobacter venezius and Marinococcus dehydrocarbons with deposit registration number 1A03971 were respectively inoculated into 15mL culture tubes containing 2mL liquid HLB, and the culture tubes were placed on a shaking shaker at 20°C and 180r / min. Incubate for 48 hours. Then, the obtained bacterial liquid was streaked in the solid medium of the activated strain and placed in a constant temperature incubator at 20°C for rejuvenation for 24 hours. The colonies on the plate were each inoculated into 15mL culture tubes containing 2mL liquid HLB and placed at 20°C. Cultured overnight in a shaking shaker at 180r / min.
[0068] Secondly, inocula...
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