Stable Escherichia coli-Clostridium acetobutylicum Shuttle Vector for Secretion of Murine Tumor Necrosis Factor Alpha

Author:

Theys J.1,Nuyts S.2,Landuyt W.2,Van Mellaert L.1,Dillen C.3,Böhringer M.4,Dürre P.4,Lambin P.2,Anné J.1

Affiliation:

1. Laboratories of Bacteriology1 and

2. Experimental Radiobiology, University Hospital Gasthuisberg,2Leuven, Belgium, and

3. Immunobiology,3 Rega Institute, Katholieke Universiteit Leuven, and

4. Microbiology and Biotechnology, University Ulm, Ulm, Germany4

Abstract

ABSTRACT Recombinant plasmids were constructed to secrete mouse tumor necrosis factor alpha (mTNF-α) from Clostridium acetobutylicum . The shuttle plasmids contained the clostridial endo-β1,4-glucanase ( eglA ) promoter and signal sequence that was fused in frame to the mTNF-α cDNA. The construction was first tested in Escherichia coli and then introduced in C. acetobutylicum DSM792 by electroporation. Controls confirmed the presence and stability of the recombinant plasmids in this organism. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis and an in vitro cytotoxic assay were used to monitor expression and secretion of mTNF-α during growth. Significant levels of biologically active mTNF-α were measured in both lysates and supernatants. The present report deals with investigations on the elaboration of a gene transfer system for cancer treatment using anaerobic bacteria.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

Reference40 articles.

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2. Stable inheritance of shuttle vectors based on plasmid pIM13 in a mutant strain of Clostridium acetobutylicum.;Azzedoug H.;J. Gen. Microbiol.,1992

3. Tumor necrosis factor. Characterization at the molecular, cellular and in vivo level.;Fiers W.;FEBS Lett.,1991

4. Anaerobic bacteria as a delivery system for cancer gene therapy: in vitro activation of 5-fluorocytosine by genetically engineered clostridia.;Fox M. E.;Gene Ther.,1996

5. Recombinant tumor necrosis factor: species specificity for a variety of human and murine transformed cell lines.;Fransen L.;Cell. Immunol.,1986

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