Microbial strain and method for efficiently disposing kitchen refuses
A technology of kitchen waste and microbial preparations, which is applied in the field of kitchen waste treatment and mixed bacterial strains for kitchen waste treatment. It can solve the problems of high oil content, inability to degrade well, high food residue, etc., and achieve the degradation time Short, high degradation rate, efficient degradation effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0047] Weigh 10g of the soil sample for analysis with sterilized weighing paper, add it to a triangular flask filled with 90ml of sterile water (with stones or glass beads inside), shake for 15min, that is 10 -1 concentrated soil suspension. Let stand for 30s, pipette 10 with a 1ml pipette -1 Put 1ml of the concentrated soil suspension into a 9ml sterile water tube, blow and suck 3 times and mix well, which is 10 -2 Concentration of the soil suspension, sequentially from 10 -2 serially diluted to 10 -5 , that is, a series of 10-fold soil dilutions (the operation process is aseptic). Spread soil dilutions of different concentrations on each screening medium plate and incubate at 30°C for 1-6 days. Number the single colonies of different shapes grown on the plate, and purify each strain, and finally transfer the purified strains to a slant for storage. Four strains of Bacillus subtilis, Bacillus megaterium, Bacillus licheniformis and Cellulomonas luteogenes were screened ou...
Embodiment 2
[0050] The four bacterial strains screened in Example 1 were spot-splotted on each enzyme-producing primary screening plate, cultured at 30°C for 1-2 days, observed whether there was a transparent circle around the colony, and measured the ratio of the diameter of the transparent circle to the diameter of the colony to determine The enzyme-producing ability of each strain was semi-quantitatively determined. Casein plate, grease plate and cellulose plate can directly observe the transparent circle; amylase plate needs to be observed after adding Lugol’s iodine solution.
[0051] The enzyme-producing ability of the strains screened is determined by the above-mentioned method, wherein, Bacillus subtilis (protease-producing), Bacillus megaterium (amylase-producing), Bacillus licheniformis (lipase-producing), Cellulomonas lutea (producing cellulase) all have high enzyme-producing ability.
[0052] Streak the four selected strains on the nutrient agar plate according to the combina...
Embodiment 3
[0056] By Bacillus subtilis, Bacillus megaterium, Bacillus licheniformis, Cellulomonas xanthogenes, Bacillus cereus, Bacillus firmus, Bacillus lateral sporosum totally seven groups of strains, according to the method described in embodiment 2 and 2: The ratio of 2:2:2:1:1:1 is prepared into solid microbial mixed strains or preparations, and the swill degradation experiment is carried out according to the method described in Example 2, and the remaining amount after the treatment of the previous day is measured before feeding the next day . The experimental results are as follows:
[0057] Table 1 Experimental results of treating swill with biological preparations of the present invention (unit: kg)
[0058] date sawdust Throw in slop water bacteria Residue after treatment first day 160 50 20 2 the next day 100 200 third day 51 200 fourth day 190
[0059] Total feeding amount=160+50+20+2+100...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com