Literature DB >> 15574897

Broad-host-range plasmid pJB658 can be used for industrial-level production of a secreted host-toxic single-chain antibody fragment in Escherichia coli.

H Sletta1, A Nedal, T E V Aune, H Hellebust, S Hakvåg, R Aune, T E Ellingsen, S Valla, T Brautaset.   

Abstract

In industrial scale recombinant protein production it is often of interest to be able to translocate the product to reduce downstream costs, and heterologous proteins may require the oxidative environment outside of the cytoplasm for correct folding. High-level expression combined with translocation to the periplasm is often toxic to the host, and expression systems that can be used to fine-tune the production levels are therefore important. We previously constructed vector pJB658, which harbors the broad-host-range RK2 minireplicon and the inducible Pm/xylS promoter system, and we here explore the potential of this unique system to manipulate the expression and translocation of a host-toxic single-chain antibody variable fragment with affinity for hapten 2-phenyloxazol-5-one (phOx) (scFv-phOx). Fine-tuning of scFv-phOx levels was achieved by varying the concentrations of inducers and the vector copy number and also different signal sequences. Our data show that periplasmic accumulation of scFv-phOx leads to cell lysis, and we demonstrate the importance of controlled and high expression rates to achieve high product yields. By optimizing such parameters we show that soluble scFv-phOx could be produced to a high volumetric yield (1.2 g/liter) in high-cell-density cultures of Escherichia coli.

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Year:  2004        PMID: 15574897      PMCID: PMC535149          DOI: 10.1128/AEM.70.12.7033-7039.2004

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  29 in total

Review 1.  Production of antibodies and antibody fragments in Escherichia coli and a comparison of their functions, uses and modification.

Authors:  David P Humphreys
Journal:  Curr Opin Drug Discov Devel       Date:  2003-03

2.  Identification of factors impeding the production of a single-chain antibody fragment in Escherichia coliby comparing in vivo and in vitro expression.

Authors:  P Oelschlaeger; S Lange; J Schmitt; M Siemann; M Reuss; R D Schmid
Journal:  Appl Microbiol Biotechnol       Date:  2003-01-28       Impact factor: 4.813

3.  Engineering stable cytoplasmic intrabodies with designed specificity.

Authors:  Marcello Donini; Veronica Morea; Angiola Desiderio; Dimitre Pashkoulov; Maria Elena Villani; Anna Tramontano; Eugenio Benvenuto
Journal:  J Mol Biol       Date:  2003-07-04       Impact factor: 5.469

Review 4.  Phage display of antibody fragments.

Authors:  A Pini; L Bracci
Journal:  Curr Protein Pept Sci       Date:  2000-09       Impact factor: 3.272

5.  Factors determining more efficient large-scale release of a periplasmic enzyme from E. coli using lysozyme.

Authors:  J J Pierce; C Turner; E Keshavarz-Moore; P Dunnill
Journal:  J Biotechnol       Date:  1997-10-02       Impact factor: 3.307

6.  High level production of soluble single chain antibodies in small-scale Escherichia coli cultures.

Authors:  S M Kipriyanov; G Moldenhauer; M Little
Journal:  J Immunol Methods       Date:  1997-01-15       Impact factor: 2.303

7.  Escherichia coli secretion of an active chimeric antibody fragment.

Authors:  M Better; C P Chang; R R Robinson; A H Horwitz
Journal:  Science       Date:  1988-05-20       Impact factor: 47.728

8.  High volumetric yields of functional dimeric miniantibodies in Escherichia coli, using an optimized expression vector and high-cell-density fermentation under non-limited growth conditions.

Authors:  U Horn; W Strittmatter; A Krebber; U Knüpfer; M Kujau; R Wenderoth; K Müller; S Matzku; A Plückthun; D Riesenberg
Journal:  Appl Microbiol Biotechnol       Date:  1996-12       Impact factor: 4.813

9.  Plasmid-encoded protein: the principal factor in the "metabolic burden" associated with recombinant bacteria.

Authors:  W E Bentley; N Mirjalili; D C Andersen; R H Davis; D S Kompala
Journal:  Biotechnol Bioeng       Date:  1990-03-25       Impact factor: 4.530

10.  Hapten-directed targeting to single-chain antibody receptors.

Authors:  Tian-Lu Cheng; Kuang-Wen Liao; Shey-Cherng Tzou; Chiu-Min Cheng; Bing-Mae Chen; Steve R Roffler
Journal:  Cancer Gene Ther       Date:  2004-05       Impact factor: 5.987

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  28 in total

1.  Multicopy integration and expression of heterologous genes in Methylobacterium extorquens ATCC 55366.

Authors:  Young J Choi; Denis Bourque; Lyne Morel; Denis Groleau; Carlos B Míguez
Journal:  Appl Environ Microbiol       Date:  2006-01       Impact factor: 4.792

2.  Role of the Pseudomonas fluorescens alginate lyase (AlgL) in clearing the periplasm of alginates not exported to the extracellular environment.

Authors:  Karianne Bakkevig; Håvard Sletta; Martin Gimmestad; Randi Aune; Helga Ertesvåg; Kristin Degnes; Bjørn Erik Christensen; Trond E Ellingsen; Svein Valla
Journal:  J Bacteriol       Date:  2005-12       Impact factor: 3.490

3.  Design and optimization of short DNA sequences that can be used as 5' fusion partners for high-level expression of heterologous genes in Escherichia coli.

Authors:  Veronika Kucharova; Jørgen Skancke; Trygve Brautaset; Svein Valla
Journal:  Appl Environ Microbiol       Date:  2013-08-23       Impact factor: 4.792

4.  Combinatorial engineering for heterologous gene expression.

Authors:  Friederike Zwick; Rahmi Lale; Svein Valla
Journal:  Bioengineered       Date:  2013-04-22       Impact factor: 3.269

5.  Mutational Analyses of Glucose Dehydrogenase and Glucose-6-Phosphate Dehydrogenase Genes in Pseudomonas fluorescens Reveal Their Effects on Growth and Alginate Production.

Authors:  Susan Maleki; Mali Mærk; Svein Valla; Helga Ertesvåg
Journal:  Appl Environ Microbiol       Date:  2015-03-06       Impact factor: 4.792

6.  The presence of N-terminal secretion signal sequences leads to strong stimulation of the total expression levels of three tested medically important proteins during high-cell-density cultivations of Escherichia coli.

Authors:  H Sletta; A Tøndervik; S Hakvåg; T E Vee Aune; A Nedal; R Aune; G Evensen; S Valla; T E Ellingsen; T Brautaset
Journal:  Appl Environ Microbiol       Date:  2006-12-01       Impact factor: 4.792

7.  Combinatorial mutagenesis and selection of improved signal sequences and their application for high-level production of translocated heterologous proteins in Escherichia coli.

Authors:  Tonje Marita Bjerkan Heggeset; Veronika Kucharova; Ingemar Naerdal; Svein Valla; Håvard Sletta; Trond Erling Ellingsen; Trygve Brautaset
Journal:  Appl Environ Microbiol       Date:  2012-11-09       Impact factor: 4.792

8.  Continuous control of the flow in biochemical pathways through 5' untranslated region sequence modifications in mRNA expressed from the broad-host-range promoter Pm.

Authors:  Rahmi Lale; Laila Berg; Friederike Stüttgen; Roman Netzer; Marit Stafsnes; Trygve Brautaset; Trond Erik Vee Aune; Svein Valla
Journal:  Appl Environ Microbiol       Date:  2011-02-18       Impact factor: 4.792

9.  Random mutagenesis of the PM promoter as a powerful strategy for improvement of recombinant-gene expression.

Authors:  Ingrid Bakke; Laila Berg; Trond Erik Vee Aune; Trygve Brautaset; Håvard Sletta; Anne Tøndervik; Svein Valla
Journal:  Appl Environ Microbiol       Date:  2009-02-05       Impact factor: 4.792

10.  Strategies for successful recombinant expression of disulfide bond-dependent proteins in Escherichia coli.

Authors:  Ario de Marco
Journal:  Microb Cell Fact       Date:  2009-05-14       Impact factor: 5.328

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