Method for producing alanine from recombinant Escherichia coli by the aid of glycerin
A technology of Escherichia coli and alanine, applied in the field of microbial genetic engineering, can solve the problems of long production cycle, increased food cost, large equipment investment, etc., and achieve the effect of reduced production cost and stable output
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[0057] 1) Cloning of gene fragments
[0058] Using primer sequence 1 and primer sequence 2, the gene fragment alaD was amplified, and the PCR amplification conditions were: 95°C for 30S, 62°C for 20S, 72°C for 30S, 30 cycles, and 72°C for 10 min.
[0059] 2) Construction of plasmid
[0060] The amplified gene fragment was digested with different restriction enzymes KpnI and XbaI to obtain cohesive ends, and the pUC19 vector was also digested with restriction enzymes KpnI and XbaI. The digestion conditions were all at 37°C and incubated for 2 hours. Recover all the obtained gene fragments and linearized vectors, mix the purified gene fragments and linearized vectors at equal concentrations, add ligation buffer and DNA ligase, and connect overnight at 37°C; obtain plasmid pALA ligation solution ;
[0061] 3) Screening of positive clones
[0062] The obtained plasmid pALA connection solution was transformed into E. coli cells by heat shock method. The specific method was as f...
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