Method for preparing (R)-phenylglycol from SD-AS sequence coupled (R)-carbonyl reductase and glucose dehydrogenase
A technology of phenylethylene glycol and hydroxyacetophenone, applied in the field of biocatalytic asymmetric transformation, can solve the problems of unstable chemical properties and expensive coenzymes
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Embodiment 1
[0065] recombine E. coli JM109 / pET-RCR and recombination E. coli The medium composition of JM109 / pET-GDH in g / L: peptone 10, yeast extract 5, NaCl 10, pH 7.0, prepared with deionized water.
[0066]The two recombinant bacteria were respectively inoculated into test tubes with a liquid volume of 5 mL of medium, and shaken at 37 °C and 200 rpm for 8 h.
Embodiment 2
[0068] recombine E. coli JM109 / pET-RCR and recombination E. coli Extraction of JM109 / pET-GDH plasmid: Centrifuge the bacteria cultured in Example 1 at 12,000 rpm for 1 min to collect the cells, and use the plasmid extraction kit Mini-Plasmid Rapid Isolation Kit (Beijing Broadtech Biogene Technology Co., Ltd.) to extract Plasmids pET-RCR and pET-GDH.
Embodiment 3
[0070] RCR and GDH co-expression primer design:
[0071] R-SD-AS-G-f: 5'-ATCCT GCTAG C ATGTCAATT CCATCAAGCC AGTAC-3'( Nhe I),
[0072] RCR-r: 5'-CGGATACAT G GTATATCTCC TTC CTATGGATTAAAAACAA
[0073] CTCTACCTT-3', (the underlined part is the reverse mutual SD-AS sequence)
[0074] GDH-f: 5'-AATCCATAG G AAGGAGATAT ACC ATGTATC CGGATTTAAA AGGAAAAGTC-3', (the underlined part is SD-AS sequence)
[0075] R-SD-AS-G-r: 5'-TGACT CTCGA G ACCGCGGCC TGCCTG-3'( xho I).
[0076] The SD-AS sequences were introduced into the primers respectively.
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