Lipase gene, recombinant expression vector, recombinant expression strain, lipase and preparation method thereof and preparation method of biodiesel
A technology of lipase gene and expression vector, applied in the field of genetic engineering, can solve the problem that heterologous genes are difficult to obtain high-efficiency expression, and achieve the effects of high yield, simple preparation process and increased expression amount
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[0055] The present invention also proposes a method for preparing the above-mentioned recombinant expression vector, comprising the following steps:
[0056] Step S11, linking the synthesized lipase gene TLLsyn to the intermediate vector pUC57 through the restriction site EcoR Ⅰ to obtain the pUC-TLLsyn vector;
[0057] First, add restriction sites EcoR Ⅰ to both ends of the synthetic lipase gene TLLsyn, and after EcoR Ⅰ digestion, connect to the intermediate vector pUC57 that has also been digested by EcoR Ⅰ to obtain the pUC-TLLsyn vector.
[0058] Step S12, digesting the pUC-TLLsyn vector and the pAO815 vector with EcoR I respectively, electrophoresis and gel recovery of lipase gene TLLsyn fragment and pAO815 fragment;
[0059] Optionally, in steps S11 and S12, the enzyme digestion system is: 30 μL of vector, 2 μL of EcoRI, 10 μL of 10×Buffer, ddH 2 Make up to 200 μL with O, and digest for about 2 hours at 37°C.
[0060] Step S13, linking the lipase gene TLLsyn fragment a...
Embodiment 1
[0086] The construction of lipase gene TLLsyn single-copy recombinant expression strain is as follows:
[0087] (1) Design the lipase gene TLLsyn sequence with the aid of DNA2.0 software, and obtain the lipase gene TLLsyn fragment by artificial synthesis.
[0088] (2) Add restriction site EcoR I to both ends of the synthesized TLLsyn gene, and after EcoR I digestion, connect to the intermediate carrier pUC57 carrier (Suzhou Jinweizhi Biotechnology Co., Ltd.) after EcoR I restriction, The pUC-TLLsyn vector was obtained; the enzyme digestion system was: 30 μL of vector, 2 μL of EcoR I, 10 μL of 10×Buffer, ddH 2 Make up to 200 μL with O, and digest for 2 hours at 37°C.
[0089] (3) The pUC-TLLsyn vector and the pAO815 vector (purchased from Invitrogen, USA, the map is as follows figure 1 (shown) were digested with EcoRI, electrophoresis, gel recovery of the lipase gene TLLsyn fragment and pAO815 fragment; wherein, the enzyme digestion system was: 30 μL of vector, 2 μL of EcoRI,...
Embodiment 2
[0094] The construction of lipase gene TLLsyn multi-copy recombinant expression strain is as follows:
[0095] (1) After the pAO815-TLLsyn recombinant expression vector single copy recombinant expression vector obtained in Example 1 was digested with Bgl II and BamH I, the large fragment was recovered from the gel to obtain the pAO815-TLLsyn recombinant expression vector fragment, wherein the enzyme digestion system For: 30 μL pAO815-TLLsyn recombinant expression vector, 1.5 μL BamH I, 1.5 μL Bgl II, 20 μL 10×Buffer K, 20 μL BSA, 20 μL Triton X-100, ddH 2 Make up to 200 μL with O, and digest for 4 hours at 37°C.
[0096] (2) Gel recovery after the new pAO815-TLLsyn recombinant expression vector recombinant expression vector is digested with BamH I, and it is connected with the pAO815-TLLsyn recombinant expression vector fragment obtained in step (1) with T4DNA ligase to obtain lipase-containing The pAO815-TLLsyn recombinant expression vector of the gene TLLsyn two copies of t...
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