Preparation method and application of sludge petroleum degrading complex enzyme
A technology of petroleum degradation and compound enzymes, applied in the field of soil treatment, can solve the problems of poor prospects and high application costs, and achieve the effects of high-efficiency oil pollution treatment capacity, low production costs, and broad application prospects.
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Embodiment 1
[0053] Acinetobacter calcoacetate ( Acinetobacter calcoaceticus ) cells were cultured and prepared as follows:
[0054] a. Acinetobacter calcium acetate ( Acinetobacter calcoaceticus ) was transferred to LB medium according to the mass ratio of 2%, and the seeds were cultured at 30°C and 160rpm for 15 hours to obtain the seed solution;
[0055] b. Transfer the seed solution prepared in step a to LB medium with an inoculum size of 4% to 5% by mass, and expand the culture at 30°C and 160rpm for 15 hours to obtain a bacterial solution;
[0056] C, the bacterium liquid that step b is made is through centrifugation, collects precipitation, makes Acinetobacter calcoacetate ( Acinetobacter calcoaceticus ) cells.
Embodiment 2
[0058] formate dehydrogenase Cb The preparation steps of FDH are as follows:
[0059] (i) Construction of genetically engineered strain Escherichia coli E. coli BL21- fdh ; The construction method is as follows:
[0060] Amplified from Candida boidinii ( Candida boidinii ) formate dehydrogenase gene fdh , the gene sequence is shown in SEQ ID NO.2, the upstream amplification primer sequence is shown in SEQ ID NO.3, the amplified formate dehydrogenase gene fdh Linked to E. coli expression vector pET28a(+), constructed to carry fdh Gene recombinant expression vector pET28a(+)- fdh , transform the host bacteria Escherichia coli BL21 (DE3), pick the transformants, and screen to obtain recombinant Escherichia coli expressing formate dehydrogenase E. coli BL21- fdh ; Refer to the instructions for use of Escherichia coli expression vector pET28a(+) for specific step conditions;
[0061] (ii) The genetically engineered strain Escherichia coli constructed in step (i...
Embodiment 3
[0070] A kind of preparation method of sludge oil degradation compound enzyme, the steps are as follows:
[0071] (1) Acinetobacter calcium acetate prepared in Example 1 ( Acinetobacter calcoaceticus ) cells were crushed, centrifuged at 5000 r / min for 2 min, and the supernatant was taken to obtain the petroleum degrading enzyme solution 21 # ;
[0072] The cells are broken, and the steps are as follows:
[0073] Acinetobacter calcoacetate ( Acinetobacter calcoaceticus ) cells were mixed evenly with phosphate buffer solution at pH 7.5 at a mass volume ratio of 1:20, unit g / ml; under 320 W ultrasonic conditions, the cells were disrupted by intermittent ultrasonic treatment for 17 min, each time ultrasonic Time 2s, intermittent time 2s;
[0074] (2) The petroleum degradation enzyme liquid 21 prepared in step (1) # It is mixed with formate dehydrogenase at a ratio of protein mass ratio of 1:4 to prepare sludge oil degradation compound enzyme.
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