Achromobacter xylosoxidans and application thereof for degrading o-aminobenzoic acid
A technology of anthranilic acid and achromobacter, which is applied in the direction of microorganism-based methods, bacteria, chemical instruments and methods, etc., can solve the problems of increased BOD, failure to meet emission standards, and failure to control the decolorized product anthranilic acid, etc. , to achieve the effect of high degradation efficiency and low cost
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[0016] Example 1. Isolation, purification and identification of Achromobacter xylosoxidans N4 CGMCC No. 3632.
[0017] In May 2009, the activated sludge in the denim printing and dyeing wastewater treatment tank (collected from a denim printing and dyeing factory in Haining, Zhejiang Province) was diluted with sterile water and coated with solid medium (1L solid medium containing 3g beef extract, Peptone 10g, NaCl 5g, agar 15g, the rest is water) plate, isolated 18 strains, using the method of streaking the plate to purify the strains. The 18 strains isolated and purified were connected to the liquid culture medium (1L medium containing beef extract 3g, peptone 10g, NaCl 5g, and the rest are water) with an inoculating loop for liquid culture. The culture temperature was 28℃ and 180rpm cultured for 24h. , Adding 5% (volume percentage) inoculum to the anthranilic acid aqueous solution, the liquid chromatography measurement results show that the N4 strain can quickly and efficiently...
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[0022] Example 2. Verification test of the effect of Achromobacter xylosoxidans N4 CGMCC №.3632 on the degradation of anthranilic acid
[0023] The culture medium of Achromobacter xylosoxidans N4 CGMCC №.3632:
[0024] Solid medium (1L): beef extract 3g, peptone 10g, NaCl 5g, agar 15g, the rest is water.
[0025] Liquid medium (1L): 3g beef extract, 10g peptone, 5g NaCl, and the rest is water.
[0026] 1. Degradation of 100mg / L anthranilic acid solution by Achromobacter xylosoxidans N4 CGMCC №.3632
[0027] Inoculate Achromobacter xylosoxidans N4CGMCC №.3632 into liquid culture medium, culture it at 28℃, 180rpm for 24-48h, to the OD of culture medium 600 Then in a non-sterile environment, the culture solution was inoculated into a 100mg / L anthranilic acid aqueous solution at 5% by volume. The control group was added with 5% by volume distilled water at 28°C at 180rpm Shake or stand still, take samples and centrifuge at different times, filter the supernatant with 0.22um microporous mem...
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