Recombinant Yarrowia lipolytica producing (-)-α-bisabolol and its construction method and application
A technology for lipolysis of Yarrowia and bisabolol, applied in the field of bioengineering, can solve the problems of the reduction of the number of eucalyptus brasiliensis, the complicated chemical synthesis steps, the difficulty of subsequent chiral separation, etc., so as to enhance the ability of homologous recombination and improve the genetic Stability, efficient construction methods
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Embodiment 1
[0032] Embodiment 1, the amplification of gene element and the preparation of target plasmid
[0033] (1) Preparation of target gene
[0034] According to the nucleotide sequence of the (-)-α-bisabolol synthase coding gene MrBBS provided by NCBI, after codon optimization, entrust Suzhou Jinweizhi Biotechnology Co., Ltd. to synthesize the optimized (-)-α- Bisabolol synthase encoding gene OptBBS was inserted into plasmid pUC57 to obtain plasmid pUC57-OptBBS. The nucleotide sequence of OptBBS is shown in SEQ ID NO.1.
[0035] According to the nucleotide sequence (M37309.1) of the 3(β)-isopropylmalate dehydrogenase coding gene leu in Yarrowia lipolytica provided by NCBI, Suzhou Jinweizhi Biotechnology Co., Ltd. was entrusted to synthesize leu, and 3( β)-Isopropylmalate dehydrogenase encoding gene expression cassette was inserted into plasmid pUC57 to obtain plasmid pUC57-leu.
[0036] According to the nucleotide sequence (genebank accession number AJ306421.1) and hisG tag (gene...
Embodiment 2
[0086] The construction of embodiment 2 recombinant bacteria
[0087] (1) Construction of Recombinant Bacteria 1
[0088] (1) The plasmid pUC-leu-A08-OptBBS containing the OptBBS gene expression cassette was introduced into Yarrowialipolytica Po1fΔku70, and the OptBBS expression cassette was integrated into the A08 site of the genome to obtain recombinant bacterium 1. The specific method is as follows: (1) Yarrowia lipolytica Po1fΔku70 was cultured overnight in YPD liquid medium (containing 2% peptone, 1% yeast extract and 2% glucose) to prepare competent cells. (2) Transform pUC-leu-A08-OptBBS into Yarrowia lipolytica Po1fΔku70 using the Zymogen Frozen EZ Yeast Transformation Kit II of Zymo Research Corporation for homologous recombination. (3) The screening medium SD-Leu was used to screen, and the positive clone identified by PCR was named recombinant bacteria 1. The screening medium SD-Leu contains: glucose 20g / L, YeastNitrogen Base (YNB, yeast nitrogen base ammonium sul...
Embodiment 3
[0124] Embodiment 3, the application of recombinant bacteria 1-8 in the production of (-)-α-bisabolol
[0125] 1. Cultivation of engineering bacteria and product extraction
[0126] The recombinant bacteria 1-8 in Example 2 were used to produce (-)-α-bisabolol respectively. The specific method is as follows: activate the recombinant bacteria, culture in YPD liquid medium at 30° C. and 220 rpm for 16 hours to obtain seed liquid. The seed solution was inoculated in 50 ml of fermentation medium with an inoculum size of 1%, and cultured with shaking at 30° C. and 220 rpm for 1 day, then added n-dodecane with 10% of the volume of the fermentation liquid, and continued shaking for 3 days. After the fermentation, the fermentation broth was transferred to a 50ml centrifuge tube, centrifuged at 5000rpm for 15min, and the organic phase was collected for later use.
[0127] Wherein the fermentation medium contains 55g / L glucose, 10g / L yeast extract and 20g / L tryptone. 2. Qualitative a...
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