Cargando…
Efficient production of soluble recombinant single chain Fv fragments by a Pseudomonas putida strain KT2440 cell factory
BACKGROUND: Recombinant antibody fragments have a wide range of applications in research, diagnostics and therapy. For many of these, small fragments like single chain fragment variables (scFv) function well and can be produced inexpensively in bacterial expression systems. Although Escherichia coli...
Autores principales: | , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3053225/ https://www.ncbi.nlm.nih.gov/pubmed/21338491 http://dx.doi.org/10.1186/1475-2859-10-11 |
_version_ | 1782199712765444096 |
---|---|
author | Dammeyer, Thorben Steinwand, Miriam Krüger, Sarah-C Dübel, Stefan Hust, Michael Timmis, Kenneth N |
author_facet | Dammeyer, Thorben Steinwand, Miriam Krüger, Sarah-C Dübel, Stefan Hust, Michael Timmis, Kenneth N |
author_sort | Dammeyer, Thorben |
collection | PubMed |
description | BACKGROUND: Recombinant antibody fragments have a wide range of applications in research, diagnostics and therapy. For many of these, small fragments like single chain fragment variables (scFv) function well and can be produced inexpensively in bacterial expression systems. Although Escherichia coli K-12 production systems are convenient, yields of different fragments, even those produced from codon-optimized expression systems, vary significantly. Where yields are inadequate, alternative production systems are needed. Pseudomonas putida strain KT2440 is a versatile biosafety strain known for good expression of heterologous genes, so we have explored its utility as a cell factory for production of scFvs. RESULTS: We have generated new broad host range scFv expression constructs and assessed their production in the Pseudomonas putida KT2440 host. Two scFvs bind either to human C-reactive protein or to mucin1, proteins of significant medical diagnostic and therapeutic interest, whereas a third is a model anti-lysozyme scFv. The KT2440 antibody expression systems produce scFvs targeted to the periplasmic space that were processed precisely and were easily recovered and purified by single-step or tandem affinity chromatography. The influence of promoter system, codon optimization for P. putida, and medium on scFv yield was examined. Yields of up to 3.5 mg/l of pure, soluble, active scFv fragments were obtained from shake flask cultures of constructs based on the original codon usage and expressed from the Ptac expression system, yields that were 2.5-4 times higher than those from equivalent cultures of an E. coli K-12 expression host. CONCLUSIONS: Pseudomonas putida KT2440 is a good cell factory for the production of scFvs, and the broad host range constructs we have produced allow yield assessment in a number of different expression hosts when yields in one initially selected are insufficient. High cell density cultivation and further optimization and refinement of the KT2440 cell factory will achieve additional increases in the yields of scFvs. |
format | Text |
id | pubmed-3053225 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30532252011-03-11 Efficient production of soluble recombinant single chain Fv fragments by a Pseudomonas putida strain KT2440 cell factory Dammeyer, Thorben Steinwand, Miriam Krüger, Sarah-C Dübel, Stefan Hust, Michael Timmis, Kenneth N Microb Cell Fact Research BACKGROUND: Recombinant antibody fragments have a wide range of applications in research, diagnostics and therapy. For many of these, small fragments like single chain fragment variables (scFv) function well and can be produced inexpensively in bacterial expression systems. Although Escherichia coli K-12 production systems are convenient, yields of different fragments, even those produced from codon-optimized expression systems, vary significantly. Where yields are inadequate, alternative production systems are needed. Pseudomonas putida strain KT2440 is a versatile biosafety strain known for good expression of heterologous genes, so we have explored its utility as a cell factory for production of scFvs. RESULTS: We have generated new broad host range scFv expression constructs and assessed their production in the Pseudomonas putida KT2440 host. Two scFvs bind either to human C-reactive protein or to mucin1, proteins of significant medical diagnostic and therapeutic interest, whereas a third is a model anti-lysozyme scFv. The KT2440 antibody expression systems produce scFvs targeted to the periplasmic space that were processed precisely and were easily recovered and purified by single-step or tandem affinity chromatography. The influence of promoter system, codon optimization for P. putida, and medium on scFv yield was examined. Yields of up to 3.5 mg/l of pure, soluble, active scFv fragments were obtained from shake flask cultures of constructs based on the original codon usage and expressed from the Ptac expression system, yields that were 2.5-4 times higher than those from equivalent cultures of an E. coli K-12 expression host. CONCLUSIONS: Pseudomonas putida KT2440 is a good cell factory for the production of scFvs, and the broad host range constructs we have produced allow yield assessment in a number of different expression hosts when yields in one initially selected are insufficient. High cell density cultivation and further optimization and refinement of the KT2440 cell factory will achieve additional increases in the yields of scFvs. BioMed Central 2011-02-21 /pmc/articles/PMC3053225/ /pubmed/21338491 http://dx.doi.org/10.1186/1475-2859-10-11 Text en Copyright ©2011 Dammeyer 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 Dammeyer, Thorben Steinwand, Miriam Krüger, Sarah-C Dübel, Stefan Hust, Michael Timmis, Kenneth N Efficient production of soluble recombinant single chain Fv fragments by a Pseudomonas putida strain KT2440 cell factory |
title | Efficient production of soluble recombinant single chain Fv fragments by a Pseudomonas putida strain KT2440 cell factory |
title_full | Efficient production of soluble recombinant single chain Fv fragments by a Pseudomonas putida strain KT2440 cell factory |
title_fullStr | Efficient production of soluble recombinant single chain Fv fragments by a Pseudomonas putida strain KT2440 cell factory |
title_full_unstemmed | Efficient production of soluble recombinant single chain Fv fragments by a Pseudomonas putida strain KT2440 cell factory |
title_short | Efficient production of soluble recombinant single chain Fv fragments by a Pseudomonas putida strain KT2440 cell factory |
title_sort | efficient production of soluble recombinant single chain fv fragments by a pseudomonas putida strain kt2440 cell factory |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3053225/ https://www.ncbi.nlm.nih.gov/pubmed/21338491 http://dx.doi.org/10.1186/1475-2859-10-11 |
work_keys_str_mv | AT dammeyerthorben efficientproductionofsolublerecombinantsinglechainfvfragmentsbyapseudomonasputidastrainkt2440cellfactory AT steinwandmiriam efficientproductionofsolublerecombinantsinglechainfvfragmentsbyapseudomonasputidastrainkt2440cellfactory AT krugersarahc efficientproductionofsolublerecombinantsinglechainfvfragmentsbyapseudomonasputidastrainkt2440cellfactory AT dubelstefan efficientproductionofsolublerecombinantsinglechainfvfragmentsbyapseudomonasputidastrainkt2440cellfactory AT hustmichael efficientproductionofsolublerecombinantsinglechainfvfragmentsbyapseudomonasputidastrainkt2440cellfactory AT timmiskennethn efficientproductionofsolublerecombinantsinglechainfvfragmentsbyapseudomonasputidastrainkt2440cellfactory |