Stenotrophomonas sp. HY-2 and application thereof in degradation of organic compounds
A technology of Stenotrophomonas and HY-2, which is applied in the field of high-efficiency new ethyl/butyl acetate degrading bacteria, can solve the problems of undiscovered high-efficiency degradation of ethyl/butyl acetate
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Embodiment 1
[0036] Example 1: Isolation, purification and identification of Stenotrophomonas HY-2
[0037] (1) Isolation and purification of Stenotrophomonas HY-2
[0038] The activated sludge from the sewage treatment tank of a pharmaceutical factory in Zhejiang was collected on site, and the lower sludge after standing still was mixed with the inorganic salt medium at a ratio of 1:2 (v / v), and the 3L mixture was connected to a 5L sludge acclimation tank (see Jin Xiaojun. Isolation and identification of new dioxane-degrading strains, degradation characteristics and preparation of bacterial agents [D]. Zhejiang University of Technology, 2012.), with ethyl acetate and butyl acetate as substrates as carbon sources and energy sources, at room temperature After nearly 20 days of domestication culture, take 5 mL of sludge from the domestication tank and add it to a shake flask containing 50 mL of inorganic salt medium. It is found that the domesticated sludge can stably degrade 110 mg / L ethyl ...
Embodiment 2
[0047] Embodiment 2: the expanded cultivation of Stenotrophomonas HY-2
[0048] 1) Slant culture: inoculate Stenotrophomonas HY-2 on the LB solid medium of the slant, and culture at 30° C. for 24-36 hours to obtain slant bacteria.
[0049] 2) Expansion culture: use an inoculation loop to pick the slant bacteria obtained in step 1) and inoculate them into LB liquid medium, culture at 30°C for 24-36 hours, and obtain OD 600 =0.1~0.2 bacteria solution.
Embodiment 3
[0050] Embodiment 3: Stenotrophomonas HY-2 degrades the performance of ethyl acetate or butyl acetate
[0051] With ethyl acetate as the sole carbon source of Stenotrophomonas HY-2, get the OD prepared by the method in Example 2 600 =0.1 bacterium liquid, inoculate to fresh 50mL inorganic salt culture medium containing 110mg / L ethyl acetate, make the initial bacterium concentration by OD 600 Calculated as 0.01, pH=7. Put it into a shaker with a temperature of 30°C and a rotation speed of 160r / min for cultivation, take samples every 3 hours to measure the degradation rate of ethyl acetate, and use a 5mL syringe to draw out a part of the bacterial liquid, and measure the OD value of the bacterial cells. The results are shown in image 3 . Under the same conditions, experiment with butyl acetate instead of ethyl acetate, the results are shown in Figure 4 . During the experiment, two parallel samples and a blank control group not inoculated with strains were designed. With t...
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