Bacillus subtilis and application thereof in manure compost deodorization
A Bacillus subtilis, compost deodorization technology, applied in the application, preparation of organic fertilizers, bacteria, etc., can solve the problems of unsatisfactory deodorization effect of deodorizing microorganisms, reduce the emission of odorous gases, and have broad application prospects. The effect of increasing the maturity
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Embodiment 1
[0033] Example 1 Screening of deodorizing bacterial strains
[0034] 1. Sample
[0035] Collected from broiler waste in Penglai, Yantai.
[0036] 2. Enrichment culture and purification of bacterial strains
[0037] Take 1g of chicken manure and add it to a culture bottle containing 99mL of sterile water, and add a few glass beads to make a suspension, then take 1mL from the suspension and put it into a culture bottle containing 50mL of enriched medium. Seal the seal and place it in a biochemical incubator at 30°C for static culture for 3-7 days. The enriched culture produces a lot of gas and has high turbidity, spread it on the separation medium, culture at 30°C for 2 days, pick out a single colony on the nutrient agar medium, and continue to purify 2 to 3 times. The purified single colonies were inoculated into 50 mL LB liquid medium respectively, and cultured at 37°C and 220 r / min for 14 hours. The number of effective viable bacteria in the fermentation broth of each str...
Embodiment 2
[0052] Identification of embodiment 2 YBS01 bacterial strain
[0053] 2.1 Identification of colony morphology
[0054] The colony morphology of YBS01 strain is as follows figure 1 As shown, the colony is light yellow, with a diameter of 5-57 mm, the colony has rough and opaque edges, and is flat in the middle. The spores are oval, partially round, and the sporangia do not expand. Cells exist alone, in pairs, or in short chains.
[0055] 2.2 16S rDNA molecular identification
[0056] The genome of YBS01 strain was extracted using a kit. Then using the genome as a template, the 16S rDNA was amplified using specific primers. The amplified PCR product was detected by 1% agarose gel electrophoresis and sent to a sequencing company for sequencing.
[0057] Sequencing results showed that the sequence of the PCR amplification product was SEQ ID NO:1. By comparing the sequence with BLAST in the NCBI database, it was found that it has the highest similarity with Bacillus subtilis...
Embodiment 3
[0064] Example 3 Evaluation of Bacillus subtilis YBS01 Enzyme Production Ability
[0065] 1. Preparation of bacteria solution
[0066] The activated Bacillus subtilis YBS01 was inoculated in LB liquid medium, cultured at 37°C and 220r / min for 14h, and the viable count was 10 8 -10 9 CFU / ml of bacterial liquid.
[0067] 2. Evaluation of Protease Production Ability
[0068] Spot the Bacillus subtilis YBS01 bacterial liquid on the agar medium containing skimmed milk, and cultivate it at 37°C for 48 hours. It can be seen that a transparent circle is formed around the Bacillus subtilis YBS01, and the diameter of the transparent circle is 25mm. This shows that Bacillus subtilis YBS01 can produce certain proteases.
[0069] Further, the Bacillus subtilis YBS01 bacterial liquid was centrifuged at 4° C. and 12000 rpm for 5 minutes, and the supernatant was obtained; the enzyme activity of protease in the fermentation supernatant of Bacillus subtilis YBS01 was detected by the following...
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