Fermentation medium and fermentation process for promoting secretory expression of HER2 affinity protein
A technology of fermentation medium and protein secretion, which is applied in the direction of fermentation, chemical instruments and methods, and methods based on microorganisms, to achieve the effects of reducing production costs, simplifying process steps, and improving product indicators
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Embodiment 1
[0048] Using gene design software, the codons of the HER2 affibody encoding gene with the pel signal peptide gene were optimized to make it suitable for recombinant expression in Escherichia coli. The HEHEHE amino acid sequence was added to the amino terminus of the HER2 Affibody, and the GGGC sequence was added to the carboxyl terminus. The length of the synthetic gene was identified by HindⅢ digestion, and the sequence of the synthetic gene was confirmed by gene sequencing. The HER2 affibody gene was cloned into pET22b(+) plasmid, and transformed into competent BL21(DE)3 Escherichia coli. The relative molecular mass of the expressed product was identified by SDS-PAGE after IPTG induced the recombinant expressing bacteria to be about 7.7kd.
[0049] The nucleotide sequence of the gene encoding the HER2 Affibody protein without the pel signal peptide is (SEQ ID No.1):
[0050] CCATGGCCCATGAACACGAGCACGAGGCGGAAAACAAATTCAACAAAGAAATGCGCAACGCGTACTGGGAAATTGCCCTGCTGCCGAACCTGACCAACC...
Embodiment 2
[0063] The secretory expression of HER2 protein comprises the following steps:
[0064] 1) Plate culture: After sterilizing the plate inoculated with the plate medium, add kanamycin at a final concentration of 50 ppm at about 50°C before cooling and solidifying, and pour the plate. Take the HER2 glycerol tube strain, smear it on the Kana-resistant plate in four divisions, and culture it overnight for 16 hours;
[0065] 2) Activated shake flask: After sterilizing and cooling the activated shake flask inoculated with the activated shake flask medium, inoculate the monoclonal and add kanamycin at a final concentration of 50ppm; pick one monoclonal on the plate, and insert kanamycin resistance In 25mL medium / 100mL shake flask, culture for 4h, OD 600 up to 1.0;
[0066] 3) Shake flasks into tanks: After sterilizing and cooling the shake flasks into tanks inoculated with the culture medium of shaker flasks into tanks, add kanamycin at a final concentration of 50 ppm at the same ti...
Embodiment 3
[0076] The secretory expression of HER2 protein comprises the following steps:
[0077] 1) 2) 3) 4) Same as Example 2, only adjusting the induction temperature to 30°C.
[0078] 5) Fermentation induction and feeding: after 5 hours of fermentation, detect OD 600 In 14.1, set the induction temperature to 30°C, start adding IPTG to start the induction, and the final concentration of the inducer is 0.5mM; and once the DO starts to rise, start feeding, and adjust the feeding speed to 35-50mL / H according to the dissolved oxygen degree, Basically control the dissolved oxygen range at 25±5% by feeding speed; for example, if the dissolved oxygen is higher than 40%, increase the feeding speed to about 50mL / H; if the dissolved oxygen is lower than 20%, reduce the feeding Speed to about 35mL / H. Induce for 8h, detect OD 600 Basically no growth after 37.3, then the induction ends and the tank is put. After induction 4h-6h-8h, samples were taken respectively, samples were prepared and ...
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