Enterobacter hallii cl2013 and method for preparing hexavalent chromium repairing bacterial agent
A technology of Enterobacter hallii and repairing bacterial agent, which is applied in the field of preparing hexavalent chromium repairing bacterial agent, and can solve the problems of high acidity, difficult to meet the standard, and high organic matter content of pressed sewage.
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Embodiment 1
[0046] A strain of Enterobacter hormaechei (Enterobacter hormaechei) CL.2013 was deposited in the General Microbiology Center of China Committee for the Collection of Microbial Cultures on January 27, 2015, with the preservation number CGMCC No.10451, address: Beichen, Chaoyang District, Beijing Institute of Microbiology, Chinese Academy of Sciences, No. 1 Yard, West Road.
[0047] The Enterobacter hallii CL.2013 is isolated and screened from the soil of the chromium slag yard. The strain was cultured on LB medium, the cell shape was rod-shaped, and Gram staining was negative; after 3 days of culture, the color of the colony was milky white, and the shape of the colony was round and smooth. After physiological and biochemical identification and 16S rDNA phylogenetic analysis, the new strain was identified and named Enterobacter hormaechei (Enterobacter hormaechei) CL.2013.
Embodiment 2
[0049] Utilize Enterobacter hallii CL.2013 of the present invention and marigold waste water, waste residue to prepare hexavalent chromium repair solid bacterial agent, and its method comprises:
[0050] (1) Prepare strain activation medium Add glucose 1g / L to LB medium, sterilize for 15-30min, and set aside;
[0051] (2) Preparation of activated seeds Insert the Enterobacterhormaechei CL.2013 strain of the present invention stored in inclined test tubes into the medium prepared in (1), at 28-35°C, 120-180r / min Shake culture for 12-16 hours to obtain activated seeds;
[0052] (3) Preparation of liquid seed culture solution Adjust the pH of the waste water to 6.5-7.5 with aqueous sodium hydroxide solution to extract lutein from marigolds, and sterilize at 115-121°C for 15-30 minutes;
[0053] (4) Preparation of liquid seeds Take the culture medium prepared in (3) and inoculate the activated seeds prepared in (2), the inoculum amount is 8%-10%, shake culture at 30-37℃, 120-200r...
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