A kind of recombinant sodium vibrio and its application
A technology of sodium-demanding vibrio and glycerol dehydratase, which is applied to recombinant sodium-demanding vibrio and its application fields, can solve the problems of complex post-extraction process, inhibition of bacterial production performance, and reduction, and achieve high yield, less by-products, Simple effect of extraction separation process
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Embodiment 1
[0061] Construction of embodiment 1 expression plasmid
[0062] 1. Construction of 1,3-propanediol synthesis module expression plasmid
[0063] Glycerol dehydratase gene dhaBCE (amino acid sequence shown in SEQ ID NO.1-3, nucleotide sequence shown in SEQ ID NO.15), glycerol dehydratase activator gene orfXY (amino acid sequence shown in SEQ ID NO.4- 5, nucleotide sequence as shown in SEQ ID NO.16) and alcohol dehydrogenase gene yqhD (amino acid sequence as shown in SEQ ID NO.6, nucleotide sequence as shown in SEQ ID NO.17) connected To the expression plasmid, construct the plasmid pTrc99a-PDO containing the synthesis module of glycerol conversion to 1,3-propanediol, the specific method is as follows:
[0064] 分别以dhaBCE-F(5'-aagcggcatgcatttacgttttgacggctagctcagtcctag gtacagtgctagcttcaccttttgagccgatgaacaatgaa-3')和dhaBCE-R(5'-cgcaccaggataacgctagcactgtacctaggactgagctagccgtcaattaattcgcctgaccggccag-3'),orfXY-F(5'-cagtcctaggtacagtgctagcgttatcctggtgcgggagagaatgatgaacaagagccaacaagttca-...
Embodiment 2
[0072] Example 2 Knocking out the arcA gene to improve the yield and yield of 1,3-propanediol produced by Narophilicus
[0073] 1. Knock out the arcA gene
[0074] Knockout the transcriptional regulator gene arcA (the amino acid sequence is shown in SEQ ID NO.11, and the nucleotide sequence is shown in SEQ ID NO.20) in Narophilus ATCC 14048. The arcA gene knockout method is as follows:
[0075] ArcA-up-F (5'-ccgaatagtctgaaccgttacgacc-3'), arcA-up-R (5'-gacagcttatcactgatcagggcggtacctaaatttgtgacaaaatt-3') and arcA-down-F (5'-aagcagctccagcctacacgtgcgctactgcacttctgtga-3') and arcA-down -R(5'-acgctttgtgacctcttgct-3') was used as a primer, and a 3.0 kb PCR fragment was respectively amplified with Narophilus ATCC 14048 as a template. Using arcA-kana-F (5'-gtcacaaatttaggtaccgccctgatcagtgataagctgtcaaacatgag-3') and arcA-kana-R (5'-cacagaagtgcagtagcgcacgtgtaggctggagctgcttc-3') as primers, a 1.3 kb PCR was amplified using plasmid pSIJ8 (purchased from Addgene) as a template fragment. ...
Embodiment 3
[0086] Example 3 Knocking out the GlpR gene to increase the yield and yield of 1,3-propanediol produced by Narophilicus
[0087] 1. Knockout the transcriptional regulator gene glpR in Narophilus ATCC 14048 and VN△arcA respectively
[0088] The glpR gene knockout method is as follows:
[0089] With glpR-up-F (5'-cggtcatccaggataaagctacagc-3'), glpR-up-R (5'-cgaagcagctccagcctacactttcggtattctcggaatcagtgg-3') and glpR-down-F (5'-tttgacagcttatcactgatcagttaggactccatgtgcacggg-3') and glpR-down -R (5'-cttactccccccctttaatagagccc-3') was used as a primer, and the 3.0kb glpR gene (amino acid sequence shown in SEQ ID NO.12, nucleotide sequence As shown in SEQ ID NO.21) upstream and downstream fragments. Using glpR-kana-F (5'-ccactgattccgagaataccgaaagtgtaggctggagctgcttc-3') and glpR-kana-R (5'-ctacccgtgcacaatggagtcctaactgatcagtgataagctgtcaaacatga ga-3') as primers, the plasmid pSIJ8 (purchased from Addgene) was used as template to amplify the 1.3 kb PCR fragments. The three fragments we...
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