Erythrocin degradation bacterium pseudomonas aeruginosa RJJ-1 and application thereof
A technology of Pseudomonas aeruginosa and erythromycin, which is applied in the direction of bacteria, water/sludge/sewage treatment, biochemical equipment and methods, etc., can solve the problems that erythromycin cannot be degraded, microorganisms cannot survive, etc. Achieve excellent social benefits and strong degradation ability
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Embodiment 1
[0025] Example 1 Screening and identification of Pseudomonas aeruginosa RJJ-1 of the present invention
[0026] 1. Screening
[0027] Weigh a certain amount of bacterial residue, add distilled water, and dilute 10 times. Take 1 mL of the supernatant, add 9 mL of sterile water for gradient dilution, and dilute to 1000 times, take the supernatant and add MSM sterile medium containing erythromycin, and place it in a shaker at 37 ° C and 180 r / min for 5 days. Spread the supernatant obtained above evenly on the MSM solid medium containing erythromycin, then put it into a 37°C incubator and culture it for 3-5 days, and separate it by streaking on an LB plate, tentatively named "erythromycin degradation Bacteria RJJ-1".
[0028] 2. Strain identification
[0029] The genomic DNA of erythromycin-degrading bacteria RJJ-1 was obtained by shaking and crushing method, and the 16S rRNA gene of the strain was amplified by PCR method and sent to Shanghai Jierui Biological Company for seque...
experiment example 1
[0054] Degradation experiment of erythromycin in experimental example 1 medium
[0055] The Pseudomonas aeruginosa RJJ-1 of the present invention is cultured in LB liquid medium, the thalline is collected by centrifugation, resuspended with sterile water, and diluted to OD 600 =1 suspension, take 1mL of the aforementioned suspension and inoculate it into 100.0mL of basic liquid inorganic salt medium containing 100mg of erythromycin, place it in a constant temperature shaker at 180r / min, and cultivate it at 37°C for 72h. The degradation rate is 68.2%. The effect of mymycin degradation efficiency is obvious ( figure 2 ).
[0056] The results of this experimental example show that Pseudomonas aeruginosa RJJ-1 can effectively degrade erythromycin.
experiment example 2
[0057] Degradation experiment of erythromycin in experimental example 2 soil
[0058] The Pseudomonas aeruginosa RJJ-1 of the present invention is cultured in LB liquid medium, the thalline is collected by centrifugation, resuspended with sterile water, and diluted to OD 600 =1 suspension, get 1mL of the aforementioned suspension and inoculate it into 100 grams of sterilized soil, and add 100mg of erythromycin, and cultivate it for 72h at 37°C. After testing, the degradation rate of erythromycin is: 46.22% ( image 3 ).
[0059] The results of this experimental example show that Pseudomonas aeruginosa RJJ-1 of the present invention can effectively degrade erythromycin in soil, and can be used for the treatment of erythromycin pollution in soil.
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