Enzymatic synthesis method for DNA phosphorothioation
A technology of phosphorothiolation and enzymatic synthesis, which is applied in the field of phosphorothiolation modification of DNA molecules, can solve the problem of no DNA phosphorothiolation modification, etc., and achieve the effect of increasing the frequency of modification
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Embodiment 1
[0033] Embodiment 1, whole cell lysate method synthesis phosphorothioylated DNA
[0034] (1), preparation of whole cell lysate
[0035] Inoculated with Salmonella ( Salmonella enterica ) serovar Cerro 87 to 200mL LB medium (Luria-Bertani medium), cultured at 37°C until A 600 is 1.5;
[0036] 4°C, 5000g centrifugation for 10 minutes to collect the bacterial cells, washed with phosphate buffer three times, washed with 20mL reaction buffer (20mM Tris-HCl, pH8.0, 60mM KCl, 10mM MgCl2, 1mM EDTA, 2mM DTT, 1mM PMSF and 25% (V / V) glycerol resuspended for later use;
[0037] The cell resuspension was repeatedly frozen and thawed 3 times, and then ultrasonically disrupted, centrifuged at 15,000 g for 20 minutes at 4°C, and the supernatant was taken. The supernatant is the whole cell lysate used to catalyze the modification of phosphorothioation of DNA.
[0038] (2), preparation of short-chain DNA substrate
[0039] The short-chain DNA synthesized by chemical method is used as the ...
Embodiment 2
[0056] Example 2. Heterologous expression and purification of protein system catalyzed synthesis of phosphorothioylated DNA
[0057] (1) Heterologous expression and purification of protein systems
[0058] from Salmonella ( Salmonella enterica ) serovar Cerro 87 amplifies four genes responsible for DNA phosphorothioylation modification, namely iscS, dptC, dptD, and dptE. Both NdeI / EcoRI restriction sites were used in the cloning primers, and the primers are shown in Table 2;
[0059] The genes of the four enzyme proteins were cloned by PCR technology, then digested with NdeI / EcoRI, and connected to the pET28-a (NOVAGEN) expression vector at the same restriction site, and then transformed with calcium chloride. The expression vector was transformed into the expression host E.coli BL21(DE3)plusS;
[0060] Induction: Pick a single colony of the transformant and inoculate it into 5 mL of LB liquid medium, and culture it on a shaker at 37°C overnight. On the second day, transfe...
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