Recombinant Bacillus subtilis for improving the production of acetylglucosamine and its construction method
A technology of Bacillus subtilis and acetyl amino, which is applied in the field of genetic engineering, can solve the problems of low conversion efficiency of acetyl glucosamine/glucose, insufficient supply of α-ketoglutarate, and low efficiency of carbon source utilization, etc., and achieve the promotion of acetyl glucosamine Effects of accumulation, reduction of by-product formation, and reduction of yield
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Embodiment 1
[0036] Construction of Bacillus subtilis BSGNKAP
[0037]According to the content disclosed in Chinese patent application 201510761678.6, B. subtilis 168ΔnagPΔgamPΔgamAΔnagAΔnagBΔldhΔpta::lox72 was used as the host, and the promoter P xylA ,P 43 Controlling the recombinant expression of glmS and GNA1, free expression of GNA1 gene with pP43-GNA1 plasmid, pM7Z6M-P xylA The -glmS plasmid integrates and expresses the glmS gene, and then knocks out the glucokinase encoding gene glck, the phosphoenolpyruvate carboxylase encoding gene pckA and the pyruvate kinase encoding gene pyk on this basis, and obtains Bacillus subtilis BSGNKAP.
Embodiment 2
[0039] Construction of recombinant Bacillus subtilis BSGNKAPM1
[0040] According to the upstream and downstream sequences of the malate dehydrogenase gene ytsJ of Bacillus subtilis 168 purchased from the American Type Microorganism Collection Center and numbered ATCC No.27370 published on NCBI (as shown in the sequence table SEQ ID NO.1-2), As well as the sequence of the bleomycin resistance gene zeo, a gene knockout frame encoding malate dehydrogenase whose sequence is shown in SEQ ID NO.9 is constructed.
[0041] The constructed malate dehydrogenase encoding gene knockout frame was transformed into the Bacillus subtilis BSGNKAP obtained in Example 1, and the bleomycin resistance in the malate dehydrogenase encoding gene knockout frame was transformed through homologous recombination. The gene zeo replaced the malate dehydrogenase gene ytsJ in Bacillus subtilis BSGNKAP, which blocked the conversion of malate into pyruvate in the host bacteria. Through bleomycin resistance pl...
Embodiment 3
[0043] Construction of recombinant Bacillus subtilis BSGNKAPM2
[0044] According to the upstream and downstream sequences of the malate dehydrogenase gene ywkA of Bacillus subtilis 168 purchased from the American Type Microorganism Collection Center with the number ATCC No.27370 published on NCBI (as shown in the sequence table SEQ ID NO.3-4), As well as the sequence of the bleomycin resistance gene zeo, a gene knockout frame encoding malate dehydrogenase whose sequence is shown in SEQ ID NO.10 is constructed.
[0045] The constructed malate dehydrogenase encoding gene knockout frame was transformed into the Bacillus subtilis BSGNKAPM1 obtained in Example 2, and the bleomycin resistance in the malate dehydrogenase encoding gene knockout frame was transformed through homologous recombination The gene zeo replaced the malate dehydrogenase gene ywkA in Bacillus subtilis BSGNKAPM1, which blocked the conversion of malate into pyruvate in the host bacteria. Through bleomycin resist...
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