Production of recombinant mink growth hormone in E. coli
| Author | Affiliation |
|---|---|
Borromeo, Vitaliano | University of Milan |
Secchi, Camillo | University of Milan |
| Other(s) | ||
|---|---|---|
Dailininkas / Artist |
| Year | Start Page | End Page |
|---|---|---|
2007 | 316 | 323 |
| URI | Access Rights |
|---|---|
| https://hdl.handle.net/20.500.14911/143478 | |
| Straipsnis | Viso teksto dokumentas (institucijos intranete) / Full Text Document (Intranet Access) |
Escherichia coli cells expressing mink (Mustela vison) growth hormone were grown in a batch fermentation process. The expression level was estimated to be 27% of the total cellular protein after 3 h of induction with 1 mM isopropyl β-d-thiogalactoside (IPTG). If the expression of mink growth hormone (mGH) was induced with 0.2 mM IPTG, the concentration of target protein was slightly lower and was found to be 23% at the same time after induction. mGH expressed as inclusion bodies was solubilized in 8 M urea and renatured by dilution protocol at a protein concentration of 1.4–2.1 mg/ml in the presence of glutathione pair in a final concentration of 11.3 mM. [GSH]/[GSSG] ratio equal to 2/1 was used. Two-step purification process comprising of ion-exchange chromatography on Q-Sepharose and hydrophobic chromatography on Phenyl-Sepharose was developed. Some 25–30 mg of highly purified and biologically active mGH was obtained from 4 g of biomass. The method presented in this study allows producing large quantities of mGH and considering initiation of scientific investigation on mGH effect on mink in vivo and availability in fur industry.