A kind of cyclodextrin glucosyltransferase mutant and its application
A glucosyl and transferase technology, applied in the fields of enzyme engineering and microbial engineering, can solve the problems of low efficiency of long-chain glycosyl genistein and achieve high product specificity
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Embodiment 1
[0038] Example 1: Preparation and expression of different cyclodextrin glucosyltransferases
[0039] Specific steps are as follows:
[0040] Chemical synthesis coding amino acid sequence is shown in the gene of cyclodextrin glucosyltransferase shown in SEQ ID NO.1 (the nucleotide sequence of gene is shown in SEQ ID NO.2); The gene obtained and pET-20b (+ ) plasmids were ligated after double enzyme digestion (NcoI and XhoI), transformed into Escherichia coli JM109, the transformed product was spread on LB solid medium, cultivated at 37°C for 8h, picked transformants on LB solid medium, and inserted into Cultured in LB liquid medium, cultured at 37°C for 10 hours, extracted the plasmid, sequenced the plasmid, and obtained the recombinant plasmid pET20b-CGT with correct sequencing; transformed the recombinant plasmid pET20b-CG with correct sequencing into Escherichia coli E.coli BL21(DE3 ) to obtain recombinant Escherichia coli pET20b-CGT / E.coliBL21.
[0041] Using the whole pl...
Embodiment 2
[0073] Example 2: Product specificity of different cyclodextrin glucosyltransferases for long-chain glycosylated genistein
[0074] Specific steps are as follows:
[0075] Genistein (purchased from Sigma Company) was dissolved in dimethylsulfoxide (DMSO) to prepare a genistein solution with a final concentration of 7.5g / L; maltodextrin (purchased from Shanghai Sangon Bioengineering Co., Ltd. ) was dissolved in PBS buffer (50mM, pH 6.5) to prepare a maltodextrin solution with a final concentration of 40g / L; the freeze-dried mutants A156V / L174P, A156V / L174P / A166Y, Pure enzymes of A156V / L174P / A166V, A156V / L174P / A166G, A156V / L174P / A166K, A156S, A156L and L174M were dissolved in PBS buffer (50mM, pH 6.5) to prepare CGTase enzyme solution with a final concentration of 15U / L ; Take 300 μL genistein solution, 500 μL maltodextrin solution and 200 μL LCGTase enzyme solution and mix them in a 2 mL small tube with a cover, place on a 40°C, 120 rpm shaker and shake slowly for 20-24 hours ...
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