| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Previous Article | Next Article ![]()
Applied and Environmental Microbiology, April 2007, p. 2758-2761, Vol. 73, No. 8
0099-2240/07/$08.00+0 doi:10.1128/AEM.02844-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Alan Pavinski Bitar, and
Hélène Marquis*
Department of Microbiology and Immunology, Cornell University, Ithaca, New York 14853
Received 6 December 2006/ Accepted 12 February 2007
In this study, we developed a new mariner-based transposition system for Listeria monocytogenes. The mariner-based system has a high rate of transposition and a low rate of plasmid retention, and transposition is very random, making it an ideal tool for high-throughput transposon mutagenesis in L. monocytogenes.
Published ahead of print on 16 February 2007.
Present address: Department of Biological Sciences, Clemson University, Clemson, SC 29634.
This article has been cited by other articles:
| J. Bacteriol. | Microbiol. Mol. Biol. Rev. | Eukaryot. Cell | All ASM Journals |
|---|