Application of lactose to expression of hIGF-1 (Human Insulin-like Growth Factor-1) by high density fermentation of recombinant colon bacillus
A technology of recombinant Escherichia coli, high-density fermentation, applied in the directions of fermentation, microorganism-based methods, biochemical equipment and methods, etc., can solve the problems of difficult to grasp induction conditions, complicated mechanism of action, etc., and achieve low price and clinical incidence. high effect
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Embodiment 1
[0047] Example 1 Lactose induced expression of hIGF-1 by high-density fermentation of E.coli DH5α / pET32a(IGF-1)
[0048] The previous work of the research group used the pET vector produced by Novagen to construct and preserve the recombinant engineered bacteria E.coli DH5α / pET32a(hIGF-1) containing the exogenous hIGF-1 gene, which was confirmed by gene sequencing and could express hIGF-1 under the induction of IPTG. 1[Liao Lianming, Yang Jian, Yu Changxi, Xu Ying. Prokaryotic expression and purification of human insulin-like growth factor-1, Chinese Journal of Biochemical Medicine, 2009, 30(4): 226-229]. Example 1 This engineering bacterium was used as an object, and lactose was used instead of IPTG to induce its high-density fermentation to express hIGF-1, so as to realize the application of lactose in recombinant Escherichia coli high-density fermentation and expression of hIGF-1.
[0049] 1 material
[0050] 1.1 Strains
[0051] The engineering bacteria E.coli DH5α / pET...
Embodiment 2
[0087] Example 2 Induction of E.coli BL by lactose 21 (DE3) / pET32a(hIGF-1) express hIGF-1 by high-density fermentation
[0088] Escherichia coli E.coli B and its derivative strains are more commonly used strains in the E. coli expression system. The acid production is relatively small, the protein expression is stable, and it is more conducive to the high-density fermentation expression of foreign genes. Therefore, the research group selected the strain E.coli BL 21 (DE3) replaced the original host strain E.coli DH5α for prokaryotic expression of hIGF-1. The recombinant plasmid pET32a(hIGF-1) containing hIGF-1 gene was extracted from the original engineering strain and then transformed into E.coli BL 21 (DE3) Competent cells, positive transformants were screened by ampicillin plate and confirmed by gene sequencing, and the engineering strain E.coli BL expressing hIGF-1 was obtained 21 (DE3) / pET32a(hIGF-1). It was then induced to express hIGF-1 in a high-density ferme...
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