Preparation method of biodiesel and compound enzyme used by preparation method
A biodiesel and compound enzyme technology, applied in the field of compound enzymes, can solve problems such as industrial application limitations and high prices, and achieve the effects of overcoming substrate specificity, easy separation, and environmental friendliness
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Embodiment 1
[0026] Embodiment 1: the cloning of CALB gene,
[0027] Primers: Upstream primer: 5'-CCCGAATTCGCCACTCCTTTGGTGAAGC-3' (contains EcoRI restriction site); downstream primer: 5'-CCCGGTACCTCAGGGGGTGACGATGCCGGAGCAG-3' (contains KpnI restriction site).
[0028] PCR reaction system: 1 μL Candida antarctica (NRRL No.Y-7954) genomic DNA, 1 μL upstream primer, 1 μL downstream primer, 25 μL Premix ExTaq, 22 μL ultrapure water.
[0029] PCR reaction conditions: Denaturation at 94°C for 10 min; denaturation at 94°C for 30 sec, annealing at 56°C for 30 sec, extension at 72°C for 1 min, 30 cycles; extension at 72°C for 10 min; incubation at 4°C.
[0030] The yield and specificity of the PCR products were detected by 1% agarose gel electrophoresis, and purified with a PCR product recovery kit (BIOMIGA, Shanghai).
[0031] The purified PCR amplification product was ligated with the cloning vector pMD-19T, and the ligated liquid was electrotransformed into E. coli-TOP10 competent cells, and a s...
Embodiment 2
[0032] Embodiment 2: the cloning of ROL gene,
[0033] Primers: Upstream primer: 5'-CCCGAATTCATGGTTCCTGTTTCTGGTAAATC-3' (contains EcoR I restriction site); downstream primer: 5'-CCCTCTAGATTACAAACAGCTTCCTTCGT-3' (contains Xba I restriction site), PCR reaction system: 1 μL R. oryzae (DSM 853) genomic DNA, 1 μL upstream primer, 1 μL downstream primer, 25 μL Premix ExTaq, 22 μL ultrapure water.
[0034] PCR reaction conditions: Denaturation at 94°C for 2 min; denaturation at 94°C for 30 sec, annealing at 52°C for 1 min, extension at 72°C for 1 min, 30 cycles; extension at 72°C for 10 min; incubation at 4°C.
[0035] The yield and specificity of the PCR products were detected by 1% agarose gel electrophoresis, and purified with a PCR product recovery kit (BIOMIGA, Shanghai).
[0036] The purified PCR amplification product was ligated with the cloning vector pMD-18T, and the ligated liquid was electrotransformed into E. coli-TOP10 (NOVAGEN) competent cells, and a small amount of pl...
Embodiment 3
[0037] Example 3: Construction of Pichia pastoris expression vector.
[0038]Use the designed primers with restriction sites (same as in Examples 1 and 2), and use the constructed pMD19T-CALB (Example 1) and pMD18T-ROL (Example 2) recombinant plasmids as templates to perform PCR Amplify (the reaction system and conditions are the same as in Examples 1 and 2), detect by gel electrophoresis, and recover the PCR amplification product by tapping the gel. The purified sample of the PCR product of the target gene and the vector pPICZαA (purchased from Invitrogen) were subjected to double enzyme digestion (the restriction sites used by CALB are EcoR I and Kpn I, and the restriction sites used by ROL are EcoR I and Xba I).
[0039] The digested PCR products were resuspended with the pPICZαA vector after concentration and added to 8 μL of sterile water, 1 μL of 10× Ligase Buffer and 1 μL of Ligase were added, and ligated overnight at 16°C. Transfer the ligated solution into E. coli-TO...
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