Pseudomonas monteilii KY-05 and application thereof
A technology of Pseudomonas montseri and strains, applied in bacteria, biochemical equipment and methods, microorganisms, etc., can solve the problems of unreported cellulose degradation and degradation function, high operating costs, secondary pollution, etc. The effect of increasing gas production and anaerobic reaction start-up speed and wide application prospects
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Embodiment 1
[0031] Screening and identification of Pseudomonas monteilii KY-05.
[0032] The experimental materials come from the anaerobic activated sludge samples of Tianjin Jizhuangzi Wastewater Treatment Plant.
[0033] Take sample diluent (dilution factor 10 -6 ) 0.1ml, spread on the screening medium plate, cultivate in a 30°C incubator, pick a single colony and inoculate it into the screening medium, intensify the culture for more than 48 hours, and repeat the streak purification 3 times to obtain the purified strain; after 16S rDNA And Biolog microbial classification and identification system identification, determined to be Pseudomonas monsonii KY-05, the phylogenetic tree is as follows figure 1 As shown, its 16S rDNA gene was amplified by PCR, and the sequencing result was shown as the sequence 1, namely:
[0034] 5'-TCTTCGGATTGTAAAGCACTTTAAGTTGGGAGGAAGGGCAGTAAGTTAATACCTTGCTGTTTTGACGTTACCGACAGAATAAGCACCGGCTAACTCTGTGCCAGCAGCCGCGGTAATACAGAGGGTGCAAGCGTTAATCGGAATTACTGGGCGTAAAGCGCGC...
Embodiment 2
[0036] Degradation test of Pseudomonas monteilii (Pseudomonas monteilii) KY-05 on macromolecular organic matter such as cellulose.
[0037] The processing object is the screening medium, and the operation mode is shaking culture in shake flasks. The specific implementation steps are as follows: Pseudomonas monsonii KY-05 described in Example 1 is inoculated to the enrichment medium, and cultured with shaking at 30° C. to the logarithmic growth phase (bacteria concentration is about 10 8 Individual / ml), inoculated in liquid screening medium with 3% inoculum size, cultured with shaking at 30°C for 1 day, and maintained dissolved oxygen at 1.0-3.0ppm; centrifuged to get supernatant as crude enzyme solution, according to DNS colorimetric method (GB / T 23881-2009) to determine the amount of reducing sugar produced by the strain degrading cellulose and other macromolecular complex organic matter. The results showed that the crude enzyme solution of the strain could produce an avera...
Embodiment 3
[0039] Synergistic experiment of Pseudomonas monteilii KY-05 on anaerobic digestion of municipal sludge.
[0040] The treatment object is anaerobic municipal sludge, and a 400mL simulated anaerobic reaction system is used for operation. The specific implementation steps are as follows: Pseudomonas monsonii KY-05 described in Example 1 is inoculated to the enrichment medium, and cultured with shaking at 30° C. to the logarithmic growth phase (bacteria concentration is about 10 8 Individuals / ml) were inoculated in a simulated anaerobic reaction system with a 0.2% inoculum amount, and operated under anaerobic conditions at a medium temperature (35±2° C.). Such as figure 2As shown, the gas production efficiency of the reaction system was monitored and compared with that of the non-inoculated group. The results showed that within 300 hours of reaction time, Staphylococcus pasteurianus KY-06 could make the mixed sludge gas production rate higher than that of the control group. Th...
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