Skip Navigation

Nucleic Acids Research 2006 34(3):e20; doi:10.1093/nar/gnj019
This Article
Right arrow Full Text Freely available
Right arrow Print PDF (683K) Freely available
Right arrow Screen PDF (156K) 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 arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Khodakaramian, G.
Right arrow Articles by Smith, M. C. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Khodakaramian, G.
Right arrow Articles by Smith, M. C. M.
Related Collections
Right arrow Recombination
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Published online 9 February 2006

© The Author 2006. Published by Oxford University Press. All rights reserved
The online version of this article has been published under an open access model. Users are entitled to use, reproduce, disseminate, or display the open access version of this article for non-commercial purposes provided that: the original authorship is properly and fully attributed; the Journal and Oxford University Press are attributed as the original place of publication with the correct citation details given; if an article is subsequently reproduced or disseminated not in its entirety but only in part or as a derivative work this must be clearly indicated. For commercial re-use, please contact journals.permissions{at}oxfordjournals.org


Methods Online

Expression of Cre recombinase during transient phage infection permits efficient marker removal in Streptomyces

Gholam Khodakaramian, Sarah Lissenden, Bertolt Gust1, Laura Moir2, Paul A. Hoskisson2, Keith F. Chater1 and Margaret C. M. Smith2,*

Institute of Genetics, University of Nottingham Nottingham NG7 2UH, UK 1John Innes Centre, Norwich Research Park Colney Lane, Norwich NR4 7UH, UK 2Institute of Medical Sciences, University of Aberdeen Foresterhill, Aberdeen AB25 2ZD, UK

*To whom correspondence should be addressed. Tel: +44 1224 555739; Fax: + 44 1224 555844; Email: Maggie.smith{at}abdn.ac.uk

Received October 11, 2005. Revised December 12, 2005. Accepted January 19, 2006.

We report a system for the efficient removal of a marker flanked by two loxP sites in Streptomyces coelicolor, using a derivative of the temperate phage {varphi}C31 that expresses Cre recombinase during a transient infection. As the test case for this recombinant phage (called Cre-phage), we present the construction of an in-frame deletion of a gene, pglW, required for phage growth limitation or Pgl in S.coelicolor. Cre-phage was also used for marker deletion in other strains of S.coelicolor.


Present addresses: Gholam Khodakaramian, Department of Plant Protection, Abourayhan Campus, Tehran University, PO Box 11365/4117 (Pakdasht), Tehran, Iran

Bertolt Gust, Institute of Pharmacy, University of Tuebingen, Auf der Morgenstelle 8, 72076 Tuebingen, Germany


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
Appl. Environ. Microbiol.Home page
M. Leibig, B. Krismer, M. Kolb, A. Friede, F. Gotz, and R. Bertram
Marker Removal in Staphylococci via Cre Recombinase and Different lox Sites
Appl. Envir. Microbiol., March 1, 2008; 74(5): 1316 - 1323.
[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.