Application of saccharomyces rouxii gene in improving yield of HDMF produced by microorganisms
A technology of Saccharomyces ruckeri and microorganisms, applied in the field of microorganisms, can solve the problems of unsuitable factory production and high price, and achieve the effects of high safety, good fragrance and environmental friendliness
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[0035] 1.1 Construction of QOR gene overexpression recombinant plasmid, FBA gene and TPI gene overexpression recombinant plasmid
[0036] Using the Saccharomyces ruxii genome as a template, gene amplification primers are shown in Table 1, and KOD FX Neo high-fidelity enzyme was used to perform QOR gene ( figure 1 A), FBA gene ( figure 1 B) and the cloning of TPI gene ( figure 1C), the successfully cloned QOR gene, FBA gene and TPI gene target fragments were sent to Shanghai Sangon Biotechnology Co., Ltd. for sequencing, and DNAMAN 7.0 was used to splice the sequencing results. The obtained sequence was aligned with the QOR (XM_002494472.1), FBA (XM_002499162.1) and TPI (XM_002498482.1) sequences in the NCBI genome of Luxie yeast.
[0037] The sequence of the QOR gene coding region is as follows:
[0038] ATGCTTAGATCGACAATATCCTCAGTGTTCAACAAGAGGGCAACAATGGCAACCACAACTATTCCAAAGACCCAAAAAGTTATTTTGATTAACGATACTGGTAGTTATGATGTGCTGAAATACCAGGATCATCCGGTGCCTAGTATTACTGACAATGAATTATTGGTTAAAA...
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