Method for producing nicotinamide ribose phosphate transferase by fermentation
A technology of phosphoribose and nicotinamide, applied in the field of bioengineering, to achieve the effects of optimizing fermentation and culture conditions, inducing culture conditions, and increasing expression
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Embodiment 1
[0032] Embodiment 1: Construction of NAMPT production strain
[0033] The plasmid pLLP-ompA was double-digested with BamHI and NhelI, and then the nucleotide fragment encoding the NAMPT enzyme shown in SEQ ID NO. A recombinant expression vector (pLLP-ompA-NAMPT).
[0034] Carry out double enzyme digestion verification on the constructed first recombinant expression vector (pLLP-ompA-NAMPT). Carry out double enzyme digestion of pLLP-ompA-NAMPT with BamHI and NhelI. If two bands of 1.5kb and 7.5kb are produced, it proves the recombinant The expression vector was constructed successfully. For the results of the double enzyme digestion verification of the constructed first recombinant expression vector, see figure 1 . The results showed that the nucleotide fragment shown in SEQ ID NO.5 had been successfully inserted into the pLLP-ompA vector.
[0035] Plasmid pET-42a(+) was double digested with SacII and SphI, and then the nucleotide fragment encoding PARP1 protein shown in SE...
Embodiment 2
[0041] Embodiment 2: the fermentative production of NAMPT enzyme
[0042] (1) Strain activation: Streak the production strain of NAMPT enzyme prepared in Example 1 preserved at low temperature on an LB plate containing 100 μg / ml KAN and 100 μg / ml AMP, culture at 33°C for 24 hours; pick a single colony of the production strain and repeat Transfer to LB plates containing 100 μg / ml KAN and 100 μg / ml AMP by streaking, culture at 33°C for 24 hours, and set aside.
[0043] The medium formula of LB plate: peptone 10.0g, yeast powder 5.0g, NaCl 10.0g, agar 15.0g, water 1.0L.
[0044] (2) Preparation of primary seed liquid: use the inoculation loop to scrape the lawn of the production strain activated in the second step (1), inoculate it in LB liquid medium, 33°C, 200r / min, shake the flask for 12h to obtain the primary seed liquid.
[0045] LB liquid medium formula: peptone 10.0g, yeast powder 5.0g, NaCl 10.0g, water 1.0L.
[0046] (3) Preparation of secondary seed liquid: the prima...
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