Optimization of recombinant human nerve growth factor production in the psychrophilic Pseudoalteromonas haloplanktis
The optimization of production strategy is a very useful tool to attain high level of recombinant protein at a low cost. A promising biotechnological application of psychrophilic bacteria is their use as non-conventional host for the recombinant production of useful proteins. The lowering of the exp...
Published in: | Journal of Biotechnology |
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Main Authors: | , , , , |
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Format: | Article in Journal/Newspaper |
Language: | English |
Published: |
Elsevier
2006
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Online Access: | http://hdl.handle.net/2434/24842 https://doi.org/10.1016/j.jbiotec.2006.05.019 |
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author | I. Vigentini A. Merico C.M. Compagno M. L. Tutino G. Marino |
author2 | I. Vigentini A. Merico M.L. Tutino C.M. Compagno G. Marino |
author_facet | I. Vigentini A. Merico C.M. Compagno M. L. Tutino G. Marino |
author_sort | I. Vigentini |
collection | The University of Milan: Archivio Istituzionale della Ricerca (AIR) |
container_issue | 1 |
container_start_page | 141 |
container_title | Journal of Biotechnology |
container_volume | 127 |
description | The optimization of production strategy is a very useful tool to attain high level of recombinant protein at a low cost. A promising biotechnological application of psychrophilic bacteria is their use as non-conventional host for the recombinant production of useful proteins. The lowering of the expression temperature can in fact facilitate the correct folding of heterologous proteins that accumulate in insoluble form as inclusion bodies when produced in Escherichia coli. An example of such "difficult" proteins is the human nerve growth factor (hNGF). The gene encoding the mature form of hNGF was expressed in the Antarctic bacterium Pseudoalteromonas haloplanktis TAC125 at 4 degrees C. Western blotting experiments demonstrated that the protein was produced in soluble form and translocated in the periplasmic space. Furthermore, an analytical gel filtration chromatography confirmed that the recombinant protein was largely in dimeric form. For a more efficient recombinant rhNGF production, the influence of cultivation operational strategies and growth conditions (medium composition, temperature, specific growth rate) on biomass yield and recombinant protein production was investigated in batch and chemostat cultivations. The highest product yield of soluble rhNGF (7.5 Mg-NGF g(dryweight)(-1)) has been achieved in batch culture at 4 degrees C on Schatz medium with addition of tryptone and vitamins. |
format | Article in Journal/Newspaper |
genre | Antarc* Antarctic |
genre_facet | Antarc* Antarctic |
geographic | Antarctic The Antarctic |
geographic_facet | Antarctic The Antarctic |
id | ftunivmilanoair:oai:air.unimi.it:2434/24842 |
institution | Open Polar |
language | English |
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op_container_end_page | 150 |
op_doi | https://doi.org/10.1016/j.jbiotec.2006.05.019 |
op_relation | info:eu-repo/semantics/altIdentifier/pmid/16859797 info:eu-repo/semantics/altIdentifier/wos/WOS:000242683100014 volume:127 issue:1 firstpage:141 lastpage:150 journal:JOURNAL OF BIOTECHNOLOGY http://hdl.handle.net/2434/24842 doi:10.1016/j.jbiotec.2006.05.019 info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-33846232747 |
publishDate | 2006 |
publisher | Elsevier |
record_format | openpolar |
spelling | ftunivmilanoair:oai:air.unimi.it:2434/24842 2025-01-16T19:21:19+00:00 Optimization of recombinant human nerve growth factor production in the psychrophilic Pseudoalteromonas haloplanktis I. Vigentini A. Merico C.M. Compagno M. L. Tutino G. Marino I. Vigentini A. Merico M.L. Tutino C.M. Compagno G. Marino 2006-12-15 http://hdl.handle.net/2434/24842 https://doi.org/10.1016/j.jbiotec.2006.05.019 eng eng Elsevier info:eu-repo/semantics/altIdentifier/pmid/16859797 info:eu-repo/semantics/altIdentifier/wos/WOS:000242683100014 volume:127 issue:1 firstpage:141 lastpage:150 journal:JOURNAL OF BIOTECHNOLOGY http://hdl.handle.net/2434/24842 doi:10.1016/j.jbiotec.2006.05.019 info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-33846232747 Pseudoalteromonas haloplanktis TAC125 human nerve growth factor recombinant protein production fermentation Settore CHIM/11 - Chimica e Biotecnologia delle Fermentazioni info:eu-repo/semantics/article 2006 ftunivmilanoair https://doi.org/10.1016/j.jbiotec.2006.05.019 2024-01-23T23:16:24Z The optimization of production strategy is a very useful tool to attain high level of recombinant protein at a low cost. A promising biotechnological application of psychrophilic bacteria is their use as non-conventional host for the recombinant production of useful proteins. The lowering of the expression temperature can in fact facilitate the correct folding of heterologous proteins that accumulate in insoluble form as inclusion bodies when produced in Escherichia coli. An example of such "difficult" proteins is the human nerve growth factor (hNGF). The gene encoding the mature form of hNGF was expressed in the Antarctic bacterium Pseudoalteromonas haloplanktis TAC125 at 4 degrees C. Western blotting experiments demonstrated that the protein was produced in soluble form and translocated in the periplasmic space. Furthermore, an analytical gel filtration chromatography confirmed that the recombinant protein was largely in dimeric form. For a more efficient recombinant rhNGF production, the influence of cultivation operational strategies and growth conditions (medium composition, temperature, specific growth rate) on biomass yield and recombinant protein production was investigated in batch and chemostat cultivations. The highest product yield of soluble rhNGF (7.5 Mg-NGF g(dryweight)(-1)) has been achieved in batch culture at 4 degrees C on Schatz medium with addition of tryptone and vitamins. Article in Journal/Newspaper Antarc* Antarctic The University of Milan: Archivio Istituzionale della Ricerca (AIR) Antarctic The Antarctic Journal of Biotechnology 127 1 141 150 |
spellingShingle | Pseudoalteromonas haloplanktis TAC125 human nerve growth factor recombinant protein production fermentation Settore CHIM/11 - Chimica e Biotecnologia delle Fermentazioni I. Vigentini A. Merico C.M. Compagno M. L. Tutino G. Marino Optimization of recombinant human nerve growth factor production in the psychrophilic Pseudoalteromonas haloplanktis |
title | Optimization of recombinant human nerve growth factor production in the psychrophilic Pseudoalteromonas haloplanktis |
title_full | Optimization of recombinant human nerve growth factor production in the psychrophilic Pseudoalteromonas haloplanktis |
title_fullStr | Optimization of recombinant human nerve growth factor production in the psychrophilic Pseudoalteromonas haloplanktis |
title_full_unstemmed | Optimization of recombinant human nerve growth factor production in the psychrophilic Pseudoalteromonas haloplanktis |
title_short | Optimization of recombinant human nerve growth factor production in the psychrophilic Pseudoalteromonas haloplanktis |
title_sort | optimization of recombinant human nerve growth factor production in the psychrophilic pseudoalteromonas haloplanktis |
topic | Pseudoalteromonas haloplanktis TAC125 human nerve growth factor recombinant protein production fermentation Settore CHIM/11 - Chimica e Biotecnologia delle Fermentazioni |
topic_facet | Pseudoalteromonas haloplanktis TAC125 human nerve growth factor recombinant protein production fermentation Settore CHIM/11 - Chimica e Biotecnologia delle Fermentazioni |
url | http://hdl.handle.net/2434/24842 https://doi.org/10.1016/j.jbiotec.2006.05.019 |