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Current Trends in Biopharmaceuticals Production in Escherichia Coli

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Journal Biotechnol Lett
Date 2022 Jul 7
PMID 35796852
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Abstract

Since the manufacture of the first biotech product for a fledgling biopharmaceutical industry in 1982, Escherichia coli, has played an important role in the industrial production of recombinant proteins. It is now 40 years since the introduction of Humulin® for the treatment of diabetes. E. coli remains an important production host, its use as a cell factory is well established and it has become the most popular expression platform particularly for non-glycosylated therapeutic proteins. A number of significant inherent obstacles in the use of prokaryotic expression systems to produce biologics has always restricted production. These include codon usage, the absence of post-translational modifications and proteolytic processing at the cell envelope. In this review, we reflect on the contribution that this model organism has made in the production of new biotech products for human medicine. This will include new advancements in the E. coli expression system to meet the biotechnology industry requirements, such as novel engineered strains to glycosylate heterologous proteins, add disulphide bonds and express complex proteins. The biopharmaceutical market is growing rapidly, with two production systems competing for market dominance: mammalian cells and microorganisms. In the past 10 years, with increased growth of antibody-based therapies, mammalian hosts particularly CHO cells have dominated. However, with new antibody like scaffolds and mimetics emerging as future proteins of interest, E. coli has again the opportunity to be the selected as the production system of choice.

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References
1.
Assadi-Porter F, Patry S, Markley J . Efficient and rapid protein expression and purification of small high disulfide containing sweet protein brazzein in E. coli. Protein Expr Purif. 2008; 58(2):263-8. PMC: 2374762. DOI: 10.1016/j.pep.2007.11.009. View

2.
Baeshen M, Al-Hejin A, Bora R, Ahmed M, Ramadan H, Saini K . Production of Biopharmaceuticals in E. coli: Current Scenario and Future Perspectives. J Microbiol Biotechnol. 2015; 25(7):953-62. DOI: 10.4014/jmb.1412.12079. View

3.
Bhatwa A, Wang W, Hassan Y, Abraham N, Li X, Zhou T . Challenges Associated With the Formation of Recombinant Protein Inclusion Bodies in and Strategies to Address Them for Industrial Applications. Front Bioeng Biotechnol. 2021; 9:630551. PMC: 7902521. DOI: 10.3389/fbioe.2021.630551. View

4.
Bhawsinghka N, Glenn K, Schaaper R . Complete Genome Sequence of Escherichia coli BL21-AI. Microbiol Resour Announc. 2020; 9(10). PMC: 7171200. DOI: 10.1128/MRA.00009-20. View

5.
Binz H, Bakker T, Phillips D, Cornelius A, Zitt C, Gottler T . Design and characterization of MP0250, a tri-specific anti-HGF/anti-VEGF DARPin® drug candidate. MAbs. 2017; 9(8):1262-1269. PMC: 5680794. DOI: 10.1080/19420862.2017.1305529. View