Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2014 Oct 2:13:141.
doi: 10.1186/s12934-014-0141-0.

Cell factories for insulin production

Affiliations
Review

Cell factories for insulin production

Nabih A Baeshen et al. Microb Cell Fact. .

Abstract

The rapid increase in the number of diabetic patients globally and exploration of alternate insulin delivery methods such as inhalation or oral route that rely on higher doses, is bound to escalate the demand for recombinant insulin in near future. Current manufacturing technologies would be unable to meet the growing demand of affordable insulin due to limitation in production capacity and high production cost. Manufacturing of therapeutic recombinant proteins require an appropriate host organism with efficient machinery for posttranslational modifications and protein refolding. Recombinant human insulin has been produced predominantly using E. coli and Saccharomyces cerevisiae for therapeutic use in human. We would focus in this review, on various approaches that can be exploited to increase the production of a biologically active insulin and its analogues in E. coli and yeast. Transgenic plants are also very attractive expression system, which can be exploited to produce insulin in large quantities for therapeutic use in human. Plant-based expression system hold tremendous potential for high-capacity production of insulin in very cost-effective manner. Very high level of expression of biologically active proinsulin in seeds or leaves with long-term stability, offers a low-cost technology for both injectable as well as oral delivery of proinsulin.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Percentage of biopharmaceuticals produced in different expression systems [5-13].
Figure 2
Figure 2
Approval numbers of biopharmaceuticals in United States and/or European Union over the past six years with a trend line showing the mean approval rate [5-13].

References

    1. Cohen SN, Chang ACY, Boyer HW, Helling RB. Construction of biologically functional bacterial plasmids in vitro. Proc Natl Acad Sci U S A. 1973;70:3240–3244. doi: 10.1073/pnas.70.11.3240. - DOI - PMC - PubMed
    1. Nielsen J. Production of biopharmaceutical proteins by yeast. Landes Biosci Bioengineered. 2013;4(4):207–211. doi: 10.4161/bioe.22856. - DOI - PMC - PubMed
    1. Goodman M, Market watch Sales of biologics to show robust growth through to 2013. Nat Rev Drug Discov. 2009;8:837. doi: 10.1038/nrd3040. - DOI - PubMed
    1. Aggarwal S. What’s fueling the biotech engine 2010 to 2011. Nat Biotechnol. 2011;29:1083–1089. doi: 10.1038/nbt.2060. - DOI - PubMed
    1. Walsh G. Biopharmaceuticals: approvals and approval trends in 2004. Biopharm Int. 2005;18:58–65.

Publication types

MeSH terms