Universal stress protein FaUSPA gene derived from ferroplasma acidarmanus, expression vector as well as construction and application thereof
A pan-emergency protein, shuttle expression vector technology, applied in application, genetic engineering, plant genetic improvement and other directions, can solve problems such as affecting sugar and amino acid absorption
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Embodiment 1
[0016] Example 1 Synthesis of the pan-emergency protein FaUSPA gene derived from the extreme acidophilus Ferroplasma acidarmanus
[0017] On the premise of not changing the amino acid sequence, according to the specific codon characteristics of Clostridium, the pan-emergency protein FaUSPA gene (Genbank ZP_05570298.1) from the extreme acidophilic bacteria Ferroplasma acidarmanus was synthesized, primers were designed, and artificially synthesized. The primer sequence is as follows, and the primer length is about 60bp.
[0018] 1. N1100=FAUSPAI-1:Tm=54,60mer
[0019] GGA,TCC,ATG,AAG,GTC,CTC,GTC,TCC,TAT,GAT,GGT,TCT,GAA,GGT,GCT,AGA,GAA,GCT,CTC,AAG
[0020] 2. N1100=FAUSPAI-2: Tm=54,60mer
[0021] TGT, AGT, ACT, CGT, CAA, CAG, TGC, ACT, TGA, GTT, CAA, GAG, CAT, ACT, TGA, GAG, CTT, CTC, TAG, CAC
[0022] 3. N1100=FAUSPAI-3:Tm=54,60mer
[0023] CAC,TGT,TGA,CGA,GTA,CTA,CAT,CGT,CTA,CGT,CAT,TCC,AAC,TAT,CGT,TGG,TAT,CTC,TGC,TTC
[0024] 4. N1100=FAUSPAI-4:Tm=54,60mer
[0025] CTG,A...
Embodiment 2
[0042] Example 2 Construction of Escherichia coli-clostridium shuttle expression vector containing FaUSPAI gene
[0043] Based on the pSOS94 vector (Desai1999, Appl Environ Microbiol), the chloramphenicol resistance gene expression unit, the Clostridium CAC3645 gene (NC_003030) promoter, the reading frame expression unit of the FaUSPAI gene and the Bacillus subtilis pyruvate kinase (PYK, NC_000964 ) gene terminator (PYK) to replace the ctfAB and abc expression units in the pSOS94 vector after directional connection, and construct the Clostridium-E. figure 1 ), the vector is about 6670bp. The specific construction steps are as follows:
[0044] The chloramphenicol expression unit was amplified from pXYP251 (GenBank accession number AY178046, containing a medium-strength prokaryotic PGm promoter and terminator T1T2) vector. The primers are cm1:5'-AAGCTTATAACTTCGTATAATGTATGCTATACGAAG-3'; cm2:5'-TCTAGATATACGAAGATAACTTCGTATAGCATACAT-3'. The amplification conditions were 94°C for...
Embodiment 3
[0049] Embodiment 3 transformation plasmid treatment and transformation method
[0050] The Escherichia coli-clostridium shuttle expression vector pFaUSPA constructed above contains resistance to ampicillin and erythromycin, can replicate in Escherichia coli, and can screen transformed Clostridium by erythromycin. The shuttle expression vector was methylated using the methylase on the pAN1 plasmid (Mermelstein1993, Appl Environ Microbiol), which contains the δ3T methyltransferase gene from Bacillus subtilis, which can realize the methylation protection of the Clostridium expression vector , so as to avoid it being cleaved by the Cac824I restriction endonuclease in Clostridium, because this restriction site widely exists in Clostridium.
[0051] The E. coli used for the amplification of the expression vector pFaUSPA must use a methylase-deficient strain, because when some cytosine methylated DNA is transformed into common E.coli strains, the transformation efficiency will be si...
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