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Developing Gram-negative bacteria for the secretion of heterologous proteins
Gram-negative bacteria are attractive hosts for recombinant protein production because they are fast growing, easy to manipulate, and genetically stable in large cultures. However, the utility of these microbes would expand if they also could secrete the product at commercial scales. Secretion of bi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6302416/ https://www.ncbi.nlm.nih.gov/pubmed/30572895 http://dx.doi.org/10.1186/s12934-018-1041-5 |
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author | Burdette, Lisa Ann Leach, Samuel Alexander Wong, Han Teng Tullman-Ercek, Danielle |
author_facet | Burdette, Lisa Ann Leach, Samuel Alexander Wong, Han Teng Tullman-Ercek, Danielle |
author_sort | Burdette, Lisa Ann |
collection | PubMed |
description | Gram-negative bacteria are attractive hosts for recombinant protein production because they are fast growing, easy to manipulate, and genetically stable in large cultures. However, the utility of these microbes would expand if they also could secrete the product at commercial scales. Secretion of biotechnologically relevant proteins into the extracellular medium increases product purity from cell culture, decreases downstream processing requirements, and reduces overall cost. Thus, researchers are devoting significant attention to engineering Gram-negative bacteria to secrete recombinant proteins to the extracellular medium. Secretion from these bacteria operates through highly specialized systems, which are able to translocate proteins from the cytosol to the extracellular medium in either one or two steps. Building on past successes, researchers continue to increase the secretion efficiency and titer through these systems in an effort to make them viable for industrial production. Efforts include modifying the secretion tags required for recombinant protein secretion, developing methods to screen or select rapidly for clones with higher titer or efficiency, and improving reliability and robustness of high titer secretion through genetic manipulations. An additional focus is the expression of secretion machineries from pathogenic bacteria in the “workhorse” of biotechnology, Escherichia coli, to reduce handling of pathogenic strains. This review will cover recent advances toward the development of high-expressing, high-secreting Gram-negative production strains. |
format | Online Article Text |
id | pubmed-6302416 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63024162018-12-31 Developing Gram-negative bacteria for the secretion of heterologous proteins Burdette, Lisa Ann Leach, Samuel Alexander Wong, Han Teng Tullman-Ercek, Danielle Microb Cell Fact Review Gram-negative bacteria are attractive hosts for recombinant protein production because they are fast growing, easy to manipulate, and genetically stable in large cultures. However, the utility of these microbes would expand if they also could secrete the product at commercial scales. Secretion of biotechnologically relevant proteins into the extracellular medium increases product purity from cell culture, decreases downstream processing requirements, and reduces overall cost. Thus, researchers are devoting significant attention to engineering Gram-negative bacteria to secrete recombinant proteins to the extracellular medium. Secretion from these bacteria operates through highly specialized systems, which are able to translocate proteins from the cytosol to the extracellular medium in either one or two steps. Building on past successes, researchers continue to increase the secretion efficiency and titer through these systems in an effort to make them viable for industrial production. Efforts include modifying the secretion tags required for recombinant protein secretion, developing methods to screen or select rapidly for clones with higher titer or efficiency, and improving reliability and robustness of high titer secretion through genetic manipulations. An additional focus is the expression of secretion machineries from pathogenic bacteria in the “workhorse” of biotechnology, Escherichia coli, to reduce handling of pathogenic strains. This review will cover recent advances toward the development of high-expressing, high-secreting Gram-negative production strains. BioMed Central 2018-12-20 /pmc/articles/PMC6302416/ /pubmed/30572895 http://dx.doi.org/10.1186/s12934-018-1041-5 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Burdette, Lisa Ann Leach, Samuel Alexander Wong, Han Teng Tullman-Ercek, Danielle Developing Gram-negative bacteria for the secretion of heterologous proteins |
title | Developing Gram-negative bacteria for the secretion of heterologous proteins |
title_full | Developing Gram-negative bacteria for the secretion of heterologous proteins |
title_fullStr | Developing Gram-negative bacteria for the secretion of heterologous proteins |
title_full_unstemmed | Developing Gram-negative bacteria for the secretion of heterologous proteins |
title_short | Developing Gram-negative bacteria for the secretion of heterologous proteins |
title_sort | developing gram-negative bacteria for the secretion of heterologous proteins |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6302416/ https://www.ncbi.nlm.nih.gov/pubmed/30572895 http://dx.doi.org/10.1186/s12934-018-1041-5 |
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