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Recombinant expression and purification of Irisin in Escherichia coli

Published on Jun. 28, 2024Total Views: 99 times Total Downloads: 40 times Download Mobile

Author: CUI Zhengqi 1 RAO Xinyu 2 ZHANG Gerui 2 GAO Ziyang 2 WANG Long 2

Affiliation: 1. School of Pharmacy, Faculty of Medicine, Hubei University of Science and Technology, Xianning 437100, Hubei Province, China 2. School of Basic Medicine, Faculty of Medicine, Hubei University of Science and Technology, Xianning 437100, Hubei Province, China

Keywords: Irisin Escherichia coli Recombinant expression Purification

DOI: 10.12173/j.issn.1004-4337.202404124

Reference: Cui ZQ, Rao XY, Zhang GR, Gao ZY, Wang L. Recombinant expression and purification of Irisin in Escherichia coli[J]. Journal of Mathematical Medicine, 2024, 37(6): 412-417. DOI: 10.12173/j.issn.1004-4337.202404124[Article in Chinese]

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Abstract

Objective  To obtain high-yield and high-purity recombinant Irisin protein by recombinant expression and purification in Escherichia coli, and to lay a foundation for the subsequent study of Irisin function.

Methods  The CDS sequence of the Irisin gene was codon optimized for gene synthesis, and the recombinant plasmid pET-30a-Irisin was constructed by a one-step cloning and ligation method, and was transformed into Escherichia coli expression receptor cells Rosetta (DE3). The expression was induced by IPTG at a final concentration of 0.5 mM for 30 h at 15 °C and 100 rpm. The bacteria were collected at the end of induced expression, and the bacterial cells were broken by ultrasonic waves, the supernatant was obtained by centrifugation and purified by Ni-IDA agarose purification resin.

Results  The recombinant plasmid pET-30a-Irisin was successfully constructed, and the recombinant expression strain was induced by low temperature and low concentration of IPTG, and the recombinant expression product of high-purity Irisin with a yield of 105 mg/L was obtained by purification with Ni-IDA agarose purification resin.

Conclusion  The optimization of codon and induction can promote the soluble expression of Irisin recombinant protein in Escherichia coli, which lays a solid foundation for the study of its effects and mechanism on different tumor cells.

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References

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