Manganese oxidizing bacteria and application thereof
A technology of manganese oxidation and bacteria, which is applied in the direction of bacteria, chemical instruments and methods, biochemical equipment and methods, etc., can solve the problems of nutrient deficient microorganisms, affect the survival of bacterial strains and manganese oxidation activity, and achieve the effect of broad application prospects
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Embodiment 1
[0046] Example 1. Isolation, purification and identification of Pseudomonas putida QJX-1
[0047] 1. Isolation and purification of Pseudomonas putida QJX-1
[0048] Pseudomonas putida QJX-1 was obtained from the manganese ore piled soil in Xiangtan, Hunan, after domestication, separation and purification. Pseudomonas putida QJX-1 is a Gram-negative bacterium. Specific steps are as follows:
[0049] Take the soil where manganese ore is piled up in Hunan Xiangtan Manganese Mine, add 2g of soil to PYG (peptone-yeast extract-glucose) medium (peptone-yeast extract-glucose) medium (peptone, glucose, yeast extract each 0.25g / L, CaCl 2 .2H 2 O content 8mg / L, MgSO 4 .7H 2 O content 0.5g / L, MnCl 2 Content 100μM, deionized water 1L), the buffer in the medium is HEPES (N-2-Hydroxyethylpiperazine-N'-2-ethanesulfonic acid, 4-hydroxyethylpiperazineethanesulfonic acid) with a final concentration of 10-20mM , pH7.5. where MnCl 2 The solution and HEPES buffer were sterilized and adde...
Embodiment 2
[0062] Embodiment 2, Pseudomonasputida QJX-1 bacterial strain is to Mn 2+ Study on the biological oxidation characteristics of
[0063] 1. Pseudomonas putida QJX-1 strain on Mn 2+ biological oxidation
[0064] After adding Mn 2+ In the PYG medium of the present invention, investigate the manganese oxidizing bacteria (Pseudomonas putida QJX-1, preservation number: CGMCC No.6630) of the present invention to Mn 2+ oxidation capacity. It is found that the bacteria of the present invention are sensitive to Mn 2+ It has good oxidation ability and can convert Mn 2+ All are oxidized to manganese oxides which are insoluble in water. Specific steps are as follows:
[0065] 1.1) Get the bacterium liquid of 2mL manganese oxidizing bacteria of the present invention, inoculate to 100mL does not contain Mn 2+In the Erlenmeyer flask of the PYG medium, 30 ° C, 170 rpm shaking culture for 48 hours.
[0066] 1.2) Take 10 mL of the cultured bacterium solution described in step 1.1) for ...
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