A high-yielding glucosamine engineering bacterium and its construction method through homologous recombination knockout nage
A technology of glucosamine and genetically engineered bacteria, which is applied in the field of bioengineering, can solve the problems of low conversion efficiency of chitin hydrolysis, has not yet reached industrialized production, and low fermentation yield, and achieves low production cost, high production intensity, and short fermentation time Effect
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[0015] 1. Construction of recombinant plasmid pET-28a(+)-glmS-gna1
[0016] Primers used to amplify the glmS gene:
[0017] Upstream: 5'-C GA GCT C AT GTG TGG AAT TGT TGG C-3' (underlined sequence indicates restriction endonuclease recognition site Sac I)
[0018] Downstream: 5'-CCC AAG CTT TTA CTC AAC CGT AAC CGA-3' (the underlined sequence represents the restriction enzyme site Hind III).
[0019] Glucosamine synthase gene glmS was obtained by PCR using E. coli BL21 (DE3) genome (GenBank No. CP001509.3) as a template. Digest the glmS gene fragment and pET-28a(+) with restriction endonucleases Sac I and Hind III, and insert the glmS gene fragment into the Sac I and Hind III sites of plasmid pET-28a(+) by ligation reaction In between, the recombinant plasmid pET-28a(+)-glmS was obtained.
[0020] Primers used to amplify the gna1 gene:
[0021] Upstream: 5'-AAGGAGATAAGAAT GCGGCCGC ATGAGCTTAC-3' (underlined sequence indicates restriction endonuclease recognition site N...
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