Microorganism bacterium agent of deodorant use for household garbage and cultivation feces and preparation method and application
A technology for microbial inoculants and domestic waste, applied in the field of environmental microorganisms, can solve the problems of not eliminating odorous substances from the source, secondary pollution of the environment, expensive raw materials, etc. amount of effect
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[0038] The invention provides a microbial agent for deodorizing household garbage and cultured feces, a preparation method and an application. The present invention selects and breeds Saccharomyces cerevisiae and S. acid Lactobacillus, and can effectively remove ammonia and hydrogen sulfide gas in domestic garbage and feces. Bacillus natto and Bacillus subtilis screened from feces materials can produce a large amount of neutral protease, protease can effectively decompose feces proteins to produce odorous organic nitrogen, and convert it into nitrate nitrogen, So as to play a fast deodorizing substance. The white rot fungi screened from municipal garden waste can effectively degrade lignin and other difficult-to-decompose substances, and can also degrade odorous gases such as organic sulfur.
[0039] The microbial bacterial agent of the invention has strong adaptability, strong deodorizing ability and high efficiency, and is suitable for deodorizing domestic garbage, farm ani...
Embodiment 1
[0055] Step 1: Preparation of initial strain
[0056] Collect samples from domestic waste landfills and farm animal manure respectively, dilute the samples 50 times with sterile water, shake them on a shaking table at 200 RPM (rev / min) for 1-2 hours, and then set the mass fraction as 5 % of the inoculum was respectively inserted into LB medium and PDA medium for 5 days, and this was repeated 5 times, and then the enrichment solution was diluted to 10 8 ~10 10 times, spread on LB and PDA selective plates, select a single colony with typical morphology, store it on the slant of the test tube, and send it for 16SRNA identification. Five strains with good deodorizing effects were screened out in our laboratory, A, B, C, D, and E. After identification, A was Saccharomyces cerevisiae, B was Lactobacillus acidophilus, C was Bacillus subtilis, and D was sodium Bacillus bean and E are white rot fungi.
[0057] Step 2: Activation
[0058] Activation of strains stored at 4°C on slant...
Embodiment 2
[0066] Step 1: Preparation of initial strain
[0067] Collect samples from domestic waste landfills and farm animal manure respectively, dilute the samples 50 times with sterile water, shake them on a shaking table at 200 RPM (rev / min) for 1-2 hours, and then set the mass fraction as 5 % of the inoculum was respectively inserted into LB medium and PDA medium for 5 days, and this was repeated 5 times, and then the enrichment solution was diluted to 10 8 ~10 10 times, spread on LB and PDA selective plates, select a single colony with typical morphology, store it on the slant of the test tube, and send it for 16SRNA identification. Five strains with good deodorizing effects were screened out in our laboratory, A, B, C, D, and E. After identification, A was Saccharomyces cerevisiae, B was Lactobacillus acidophilus, C was Bacillus subtilis, and D was sodium Bacillus bean and E are white rot fungi.
[0068] Step 2: Activation
[0069] Activation of strains stored at 4°C on slant...
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