Escherichia coli ferritin mutant with heme removed and recombinant system containing it
A technology of Escherichia coli and heme, applied in the field of genetic engineering, can solve problems such as the influence of ferritin stability, and achieve the effect of improving temperature stability
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Embodiment 1
[0029] The preparation method of Escherichia coli ferritin mutant gene M52A:
Embodiment 2
[0033] Cloning of Escherichia coli ferritin gene M52A:
[0034] The Escherichia coli ferritin gene in the PCR amplification embodiment 1 with following pair of primers:
[0035] Upstream primer: 5'-ATCGATGAAGCGAAACATGCAGATCG-3'
[0036] Downstream primer: 5'-GCTTTCATGGTATTCCACATCGTTCAG-3'
[0037] PCR reaction system: 1 μL synthetic sequence (obtained in Example 1), 1 μL upstream primer, 1 μL downstream primer, 10 μL 5×PrimeSTARTMBuffer, 32.5 μL ddH 2 O, 4 μL dNTPs, 0.5 μL PrimeSTAR™ HS DNA polymerase.
[0038] PCR reaction conditions: 95°C for 5 min; 30 cycles of denaturation at 95°C for 30 sec, annealing at 55°C for 30 sec, and extension at 72°C for 4.5 min; extension at 72°C for 10 min; incubation at 4°C.
Embodiment 3
[0040] Verification of recombinant clone, expression vector pET32Ek / LIC-M52A (gained in Example 2):
[0041] Perform agarose gel verification of the PCR product (prepared in Example 2): prepare 10% agarose gel, add nucleic acid dye to a final concentration of 0.5 μg / mL, mix 5 μL DNA sample with 1 μL 6×Loading Buffer, carefully Add to the sample well, and add DL 10000 or 1kb ladder Marker at the same time.
[0042] Set 100-120V constant voltage electrophoresis, and stop electrophoresis when the front of bromophenol blue runs to about 1cm away from the positive end of the gel. like figure 1 As shown, there is an obvious band at 7000bp, which is consistent with the theoretical size of the target fragment, indicating that the gene has been successfully cloned.
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