Thermostable citrate synthase gene, engineered bacterium containing gene and expression method thereof
A technology of citric acid synthase and genetically engineered bacteria, applied in the field of genetic engineering, can solve the problems of unfavorable industrial production, high fermentation temperature, and high manufacturing cost, and achieve the effects of saving production cost, heat-resistant enzyme activity, and saving production conditions
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Embodiment 1
[0032] A heat-resistant citrate synthase gene, the heat-resistant citrate synthase gene has the base sequence of SEQ ID NO.1.
[0033] A genetic engineering bacterium of heat-resistant citrate synthase, the construction method of the engineering bacterium comprises primer design, construction of a recombinant expression plasmid and host bacterium transformation, the specific steps are as follows:
[0034] 1) Primer design: According to the known Anabaena sp.PCC7120 citrate synthase gene (NC_003272.1), a pair of forward primers gltAF containing an Nde I site and an Xho I site were designed The primer of the reverse primer gltAR, wherein, the sequence of the forward primer gltAF: 5'-AAATGTGCATATGATGGTGTGCGAATACAAGCCTG-3', the reverse primer gltAR: 5'-AGCCGCTCGAGTTATTTCCCCAGCTTTTAACGTTGGTCAA-3';
[0035] 2) Constructing a recombinant expression plasmid: using the whole genome DNA of Anabaena PCC 7120 as a template, using PCR amplification technology to obtain the target gene frag...
Embodiment 2
[0040]1. Determination of thermostable citrate synthase (CS): citrate synthase can catalyze the condensation of acetyl coenzyme A and oxaloacetate to generate citric acid and coenzyme A, and its activity determination method refers to the DTNB method of Srere et al. DTNB (5,5'-dithio-2-nitrobenzoic acid) is Ellman's reagent. In the presence of sulfur compounds, colorless DTNB will be transformed into yellow 5-mercapto-2-nitrobenzoic acid . Since 5-mercapto-2-nitrobenzoic acid has a maximum absorption peak at 412nm, the enzyme activity can be determined by monitoring the change of A412nm. The determination method is as follows:
[0041] Reaction system: Tris-HCL (pH 8.0), oxaloacetate, acetyl-CoA, DTNB.
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