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...

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Published in:Journal of Biotechnology
Main Authors: I. Vigentini, A. Merico, C.M. Compagno, M. L. Tutino, G. Marino
Other Authors: M.L. Tutino
Format: Article in Journal/Newspaper
Language:English
Published: Elsevier 2006
Subjects:
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
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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.
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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