Published online 9 February 2006
Methods Online |
Expression of Cre recombinase during transient phage infection permits efficient marker removal in Streptomyces
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
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
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