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Cell factories for insulin production

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...

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Autores principales: Baeshen, Nabih A, Baeshen, Mohammed N, Sheikh, Abdullah, Bora, Roop S, Ahmed, Mohamed Morsi M, Ramadan, Hassan A I, Saini, Kulvinder Singh, Redwan, Elrashdy M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4203937/
https://www.ncbi.nlm.nih.gov/pubmed/25270715
http://dx.doi.org/10.1186/s12934-014-0141-0
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author Baeshen, Nabih A
Baeshen, Mohammed N
Sheikh, Abdullah
Bora, Roop S
Ahmed, Mohamed Morsi M
Ramadan, Hassan A I
Saini, Kulvinder Singh
Redwan, Elrashdy M
author_facet Baeshen, Nabih A
Baeshen, Mohammed N
Sheikh, Abdullah
Bora, Roop S
Ahmed, Mohamed Morsi M
Ramadan, Hassan A I
Saini, Kulvinder Singh
Redwan, Elrashdy M
author_sort Baeshen, Nabih A
collection PubMed
description 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.
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spelling pubmed-42039372014-10-22 Cell factories for insulin production Baeshen, Nabih A Baeshen, Mohammed N Sheikh, Abdullah Bora, Roop S Ahmed, Mohamed Morsi M Ramadan, Hassan A I Saini, Kulvinder Singh Redwan, Elrashdy M Microb Cell Fact Review 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. BioMed Central 2014-10-02 /pmc/articles/PMC4203937/ /pubmed/25270715 http://dx.doi.org/10.1186/s12934-014-0141-0 Text en © Baeshen et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Baeshen, Nabih A
Baeshen, Mohammed N
Sheikh, Abdullah
Bora, Roop S
Ahmed, Mohamed Morsi M
Ramadan, Hassan A I
Saini, Kulvinder Singh
Redwan, Elrashdy M
Cell factories for insulin production
title Cell factories for insulin production
title_full Cell factories for insulin production
title_fullStr Cell factories for insulin production
title_full_unstemmed Cell factories for insulin production
title_short Cell factories for insulin production
title_sort cell factories for insulin production
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4203937/
https://www.ncbi.nlm.nih.gov/pubmed/25270715
http://dx.doi.org/10.1186/s12934-014-0141-0
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