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Fed-batch process for the psychrotolerant marine bacterium Pseudoalteromonas haloplanktis

BACKGROUND: Pseudoalteromonas haloplanktis is a cold-adapted γ-proteobacterium isolated from Antarctic sea ice. It is characterized by remarkably high growth rates at low temperatures. P. haloplanktis is one of the model organisms of cold-adapted bacteria and has been suggested as an alternative hos...

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Autores principales: Wilmes, Boris, Hartung, Angelika, Lalk, Michael, Liebeke, Manuel, Schweder, Thomas, Neubauer, Peter
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2954877/
https://www.ncbi.nlm.nih.gov/pubmed/20858251
http://dx.doi.org/10.1186/1475-2859-9-72
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author Wilmes, Boris
Hartung, Angelika
Lalk, Michael
Liebeke, Manuel
Schweder, Thomas
Neubauer, Peter
author_facet Wilmes, Boris
Hartung, Angelika
Lalk, Michael
Liebeke, Manuel
Schweder, Thomas
Neubauer, Peter
author_sort Wilmes, Boris
collection PubMed
description BACKGROUND: Pseudoalteromonas haloplanktis is a cold-adapted γ-proteobacterium isolated from Antarctic sea ice. It is characterized by remarkably high growth rates at low temperatures. P. haloplanktis is one of the model organisms of cold-adapted bacteria and has been suggested as an alternative host for the soluble overproduction of heterologous proteins which tend to form inclusion bodies in established expression hosts. Despite the progress in establishing P. haloplanktis as an alternative expression host the cell densities obtained with this organism, which is unable to use glucose as a carbon source, are still low. Here we present the first fed-batch cultivation strategy for this auspicious alternative expression host. RESULTS: The key for the fed-batch cultivation of P. haloplanktis was the replacement of peptone by casamino acids, which have a much higher solubility and allow a better growth control. In contrast to the peptone medium, on which P. haloplanktis showed different growth phases, on a casamino acids-containing, phosphate-buffered medium P. haloplanktis grew exponentially with a constant growth rate until the stationary phase. A fed-batch process was established by feeding of casamino acids with a constant rate resulting in a cell dry weight of about 11 g l(-1 )(OD(540 )= 28) which is a twofold increase of the highest densities which have been obtained with P. haloplanktis so far and an eightfold increase of the density obtained in standard shake flask cultures. The cell density was limited in the fed-batch cultivation by the relatively low solubility of casamino acids (about 100 g l(-1)), which was proven by pulse addition of casamino acid powder which increased the cell density to about 20 g l(-1 )(OD(540 )= 55). CONCLUSION: The growth of P. haloplanktis to higher cell densities on complex medium is possible. A first fed-batch fermentation strategy could be established which is feasible to be used in lab-scale or for industrial purposes. The substrate concentration of the feeding solution was found to influence the maximal biomass yield considerably. The bottleneck for growing P. haloplanktis to high cell densities still remains the availability of a highly concentrated substrate and the reduction of the substrate complexity. However, our results indicate glutamic acid as a major carbon source, which provides a good basis for further improvement of the fed-batch process.
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spelling pubmed-29548772010-10-15 Fed-batch process for the psychrotolerant marine bacterium Pseudoalteromonas haloplanktis Wilmes, Boris Hartung, Angelika Lalk, Michael Liebeke, Manuel Schweder, Thomas Neubauer, Peter Microb Cell Fact Research BACKGROUND: Pseudoalteromonas haloplanktis is a cold-adapted γ-proteobacterium isolated from Antarctic sea ice. It is characterized by remarkably high growth rates at low temperatures. P. haloplanktis is one of the model organisms of cold-adapted bacteria and has been suggested as an alternative host for the soluble overproduction of heterologous proteins which tend to form inclusion bodies in established expression hosts. Despite the progress in establishing P. haloplanktis as an alternative expression host the cell densities obtained with this organism, which is unable to use glucose as a carbon source, are still low. Here we present the first fed-batch cultivation strategy for this auspicious alternative expression host. RESULTS: The key for the fed-batch cultivation of P. haloplanktis was the replacement of peptone by casamino acids, which have a much higher solubility and allow a better growth control. In contrast to the peptone medium, on which P. haloplanktis showed different growth phases, on a casamino acids-containing, phosphate-buffered medium P. haloplanktis grew exponentially with a constant growth rate until the stationary phase. A fed-batch process was established by feeding of casamino acids with a constant rate resulting in a cell dry weight of about 11 g l(-1 )(OD(540 )= 28) which is a twofold increase of the highest densities which have been obtained with P. haloplanktis so far and an eightfold increase of the density obtained in standard shake flask cultures. The cell density was limited in the fed-batch cultivation by the relatively low solubility of casamino acids (about 100 g l(-1)), which was proven by pulse addition of casamino acid powder which increased the cell density to about 20 g l(-1 )(OD(540 )= 55). CONCLUSION: The growth of P. haloplanktis to higher cell densities on complex medium is possible. A first fed-batch fermentation strategy could be established which is feasible to be used in lab-scale or for industrial purposes. The substrate concentration of the feeding solution was found to influence the maximal biomass yield considerably. The bottleneck for growing P. haloplanktis to high cell densities still remains the availability of a highly concentrated substrate and the reduction of the substrate complexity. However, our results indicate glutamic acid as a major carbon source, which provides a good basis for further improvement of the fed-batch process. BioMed Central 2010-09-21 /pmc/articles/PMC2954877/ /pubmed/20858251 http://dx.doi.org/10.1186/1475-2859-9-72 Text en Copyright ©2010 Wilmes et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Wilmes, Boris
Hartung, Angelika
Lalk, Michael
Liebeke, Manuel
Schweder, Thomas
Neubauer, Peter
Fed-batch process for the psychrotolerant marine bacterium Pseudoalteromonas haloplanktis
title Fed-batch process for the psychrotolerant marine bacterium Pseudoalteromonas haloplanktis
title_full Fed-batch process for the psychrotolerant marine bacterium Pseudoalteromonas haloplanktis
title_fullStr Fed-batch process for the psychrotolerant marine bacterium Pseudoalteromonas haloplanktis
title_full_unstemmed Fed-batch process for the psychrotolerant marine bacterium Pseudoalteromonas haloplanktis
title_short Fed-batch process for the psychrotolerant marine bacterium Pseudoalteromonas haloplanktis
title_sort fed-batch process for the psychrotolerant marine bacterium pseudoalteromonas haloplanktis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2954877/
https://www.ncbi.nlm.nih.gov/pubmed/20858251
http://dx.doi.org/10.1186/1475-2859-9-72
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