Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow Print PDF (153K) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Cranenburgh, R. M.
Right arrow Articles by Sherratt, D. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Cranenburgh, R. M.
Right arrow Articles by Sherratt, D. J.
Related Collections
Right arrow Cloning
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 2001, Vol. 29, No. 5 e26
© 2001 Oxford University Press

Escherichia coli strains that allow antibiotic-free plasmid selection and maintenance by repressor titration

Rocky M. Cranenburgh1,2, Julian A. J. Hanak1,*, Steven G. Williams1 and David J. Sherratt2

1Cobra Therapeutics Ltd, The Science Park, Keele, Staffordshire ST5 5SP, UK and 2Division of Molecular Genetics, Department of Biochemistry, University of Oxford, South Parks Road, Oxford OX1 3QU, UK

We report the construction of two novel Escherichia coli strains (DH1lacdapD and DH1lacP2dapD) that facilitate the antibiotic-free selection and stable maintenance of recombinant plasmids in complex media. They contain the essential chromosomal gene, dapD, under the control of the lac operator/promoter. Unless supplemented with IPTG (which induces expression of dapD) or DAP, these cells lyse. However, when the strains are transformed with a multicopy plasmid containing the lac operator, the operator competitively titrates the LacI repressor and allows expression of dapD from the lac promoter. Thus transformants can be isolated and propagated simply by their ability to grow on any medium by repressor titration selection. No antibiotic resistance genes or other protein expressing sequences are required on the plasmid, and antibiotics are not necessary for plasmid selection, making these strains a valuable tool for therapeutic DNA and recombinant protein production. We describe the construction of these strains and demonstrate plasmid selection and maintenance by repressor titration, using the new pORT plasmid vectors designed to facilitate recombinant DNA exploitation.

* To whom correspondence should be addressed. Tel: +44 1782 714 181; Fax: +44 1782 714 167; Email: julian.hanak{at}cobrat.com


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J. Gen. Virol.Home page
W. A. Burgers, J. H. van Harmelen, E. Shephard, C. Adams, T. Mgwebi, W. Bourn, T. Hanke, A.-L. Williamson, and C. Williamson
Design and preclinical evaluation of a multigene human immunodeficiency virus type 1 subtype C DNA vaccine for clinical trial
J. Gen. Virol., February 1, 2006; 87(2): 399 - 410.
[Abstract] [Full Text] [PDF]


Home page
Infect. Immun.Home page
H. S. Garmory, M. W. Leckenby, K. F. Griffin, S. J. Elvin, R. R. Taylor, M. G. Hartley, J. A. J. Hanak, E. D. Williamson, and R. M. Cranenburgh
Antibiotic-Free Plasmid Stabilization by Operator-Repressor Titration for Vaccine Delivery by Using Live Salmonella enterica Serovar Typhimurium
Infect. Immun., April 1, 2005; 73(4): 2005 - 2011.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.