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Characterisation of the Escherichia coli membrane structure and function during fedbatch cultivation
BACKGROUND: Important parameters during recombinant protein production in Escherichia coli, such as productivity and protein activity, are affected by the growth rate. This includes the translocation of protein over the membrane to gain better folding capacity or reduced proteolysis. To vary the gro...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2004
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC514524/ https://www.ncbi.nlm.nih.gov/pubmed/15282031 http://dx.doi.org/10.1186/1475-2859-3-9 |
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author | Shokri, Atefeh Larsson, Gen |
author_facet | Shokri, Atefeh Larsson, Gen |
author_sort | Shokri, Atefeh |
collection | PubMed |
description | BACKGROUND: Important parameters during recombinant protein production in Escherichia coli, such as productivity and protein activity, are affected by the growth rate. This includes the translocation of protein over the membrane to gain better folding capacity or reduced proteolysis. To vary the growth rate two techniques are available: fedbatch and continuous cultivation, both controlled by the ingoing feed rate. RESULTS: During fedbatch cultivation, E. coli contains phosphatidylethanolamine, phosphatidylglycerol, cardiolipin and saturated fatty acids in amounts which are stable with growth rate. However, the levels of cardiolipin are very high compared to continuous cultivation. The reason for fedbatch triggering of this metabolism is not known but hypothesised to result from an additional need for carbon and energy. The reason could be the dynamic and sometimes rapid changes in growth rate to which the fedbatch cell has at all times to adjust. The membrane flexibility, essential for translocation of various components, is however to some degree sustained by production of increased amounts of unsaturated fatty acids in phosphatidylglycerol. The result is a functionally stiff membrane which generally promotes low cell lysis and is constant with respect to protein leakage to the medium. At comparatively high growth rates, when the further stabilising effect of cyclic fatty acids is gone, the high level of unsaturated fatty acids results in a pronounced effect upon sonication. This is very much in contrast to the membrane function in continuous cultivation which shows very specific characteristics as a function of growth rate. CONCLUSIONS: The stiff and unchanging fedbatch membrane should promote a stable behaviour during downstream processing and is less dependent on the time of harvest. However, optimisation of protein leakage can only be achieved in the continuously cultivated cell where leakage is twice as high compared to the constant leakage level in fedbatch. If leakage is undesired, continuous cultivation is also preferred since it can be designed to lead to the lowest values detected. Induction at low growth rate (<0.2 h(-1)) should be avoided with respect to productivity, in any system, since the specific and total protein production shows their lowest values at this point. |
format | Text |
id | pubmed-514524 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-5145242004-08-24 Characterisation of the Escherichia coli membrane structure and function during fedbatch cultivation Shokri, Atefeh Larsson, Gen Microb Cell Fact Research BACKGROUND: Important parameters during recombinant protein production in Escherichia coli, such as productivity and protein activity, are affected by the growth rate. This includes the translocation of protein over the membrane to gain better folding capacity or reduced proteolysis. To vary the growth rate two techniques are available: fedbatch and continuous cultivation, both controlled by the ingoing feed rate. RESULTS: During fedbatch cultivation, E. coli contains phosphatidylethanolamine, phosphatidylglycerol, cardiolipin and saturated fatty acids in amounts which are stable with growth rate. However, the levels of cardiolipin are very high compared to continuous cultivation. The reason for fedbatch triggering of this metabolism is not known but hypothesised to result from an additional need for carbon and energy. The reason could be the dynamic and sometimes rapid changes in growth rate to which the fedbatch cell has at all times to adjust. The membrane flexibility, essential for translocation of various components, is however to some degree sustained by production of increased amounts of unsaturated fatty acids in phosphatidylglycerol. The result is a functionally stiff membrane which generally promotes low cell lysis and is constant with respect to protein leakage to the medium. At comparatively high growth rates, when the further stabilising effect of cyclic fatty acids is gone, the high level of unsaturated fatty acids results in a pronounced effect upon sonication. This is very much in contrast to the membrane function in continuous cultivation which shows very specific characteristics as a function of growth rate. CONCLUSIONS: The stiff and unchanging fedbatch membrane should promote a stable behaviour during downstream processing and is less dependent on the time of harvest. However, optimisation of protein leakage can only be achieved in the continuously cultivated cell where leakage is twice as high compared to the constant leakage level in fedbatch. If leakage is undesired, continuous cultivation is also preferred since it can be designed to lead to the lowest values detected. Induction at low growth rate (<0.2 h(-1)) should be avoided with respect to productivity, in any system, since the specific and total protein production shows their lowest values at this point. BioMed Central 2004-07-28 /pmc/articles/PMC514524/ /pubmed/15282031 http://dx.doi.org/10.1186/1475-2859-3-9 Text en Copyright © 2004 Shokri and Larsson; licensee BioMed Central Ltd. |
spellingShingle | Research Shokri, Atefeh Larsson, Gen Characterisation of the Escherichia coli membrane structure and function during fedbatch cultivation |
title | Characterisation of the Escherichia coli membrane structure and function during fedbatch cultivation |
title_full | Characterisation of the Escherichia coli membrane structure and function during fedbatch cultivation |
title_fullStr | Characterisation of the Escherichia coli membrane structure and function during fedbatch cultivation |
title_full_unstemmed | Characterisation of the Escherichia coli membrane structure and function during fedbatch cultivation |
title_short | Characterisation of the Escherichia coli membrane structure and function during fedbatch cultivation |
title_sort | characterisation of the escherichia coli membrane structure and function during fedbatch cultivation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC514524/ https://www.ncbi.nlm.nih.gov/pubmed/15282031 http://dx.doi.org/10.1186/1475-2859-3-9 |
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