A kind of bacillus subtilis genetic engineering strain and its construction method and its application in the production of lactulose
A technology of Bacillus subtilis and genetically engineered bacteria, applied in the field of bioengineering, can solve problems such as potential safety hazards, and achieve the effects of improving productivity, reducing costs, and simplifying separation and purification
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Embodiment 1
[0038] Example 1: Synthesis of the cellobiose epimerase gene.
[0039] According to the reported gene sequence of cellobiose epimerase, the gene sequence shown in SEQ ID NO.1 was synthesized by the method of total gene synthesis.
Embodiment 2
[0040] Example 2: Construction of recombinant Bacillus subtilis.
[0041]Using the DNA obtained in Example 1 as a template, the cellobiose epimerase gene fragment was amplified. The PCR amplification system is: 2 μL of synthesized DNA, 1 μL of each primer Primer 1 and Primer 2, 2 μL of dNTP, 2.5 μL of 10×Ex-Tag buffer, 0.5 μL of Ex-Tag polymerase, ddH 2 O 14 μL. The PCR reaction program was: pre-denaturation at 94°C for 2 min, denaturation at 94°C for 2 min; then annealing at 60°C for 30 s, extension at 72°C for 1 min, and 35 cycles; extension at 72°C for 1 min.
[0042] The amplified bands were gel-cut and recovered with a column-type gel-slicing recovery kit, and the PCR product was double-digested with BamHI and SmaI. The digestion system is: 50 μL of PCR product or plasmid, 1 μL of XhoI, 1 μL of NdeI, 10 μL of 10× buffer, ddH 2 O38μL, total volume 100μL.
[0043] The digested PCR product was ligated with the pHT-01 plasmid (or pHT-43 plasmid) treated with the same rest...
Embodiment 3
[0045] Example 3: Inducible expression of cellobiose epimerase.
[0046] The constructed recombinant Bacillus subtilis str.168 (pHT-01-CsCE) was inoculated in 5 ml of LB liquid medium supplemented with ampicillin resistance, and cultivated overnight at 37°C; Ampicillin LB medium, fermented for 2 to 4 hours to OD 600 When reaching 0.6, add 0.6mmol / L isopropyl-β-D-thiogalactopyranoside (IPTG) or 10g / L lactose to continue to induce expression for 24h.
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