Xer Site-Specific Recombination, an Efficient Tool To Introduce Unmarked Deletions into Mycobacteria
Author:
Affiliation:
1. Department of Histology, Microbiology, and Medical Biotechnologies
2. Department of Biology, University of Padua, Padua, Italy
Abstract
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Link
https://journals.asm.org/doi/pdf/10.1128/AEM.00382-10
Reference24 articles.
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2. Bardarov, S., J. Kriakov, C. Carriere, S. Yu, C. Vaamonde, R. A. McAdam, B. R. Bloom, G. F. Hatfull, and W. R. Jacobs, Jr. 1997. Conditionally replicating mycobacteriophages: a system for transposon delivery to Mycobacterium tuberculosis. Proc. Natl. Acad. Sci. U. S. A.94:10961-10966.
3. Barik, S., K. Sureka, P. Mukherjee, J. Basu, and M. Kundu. 2010. RseA, the SigE specific anti-sigma factor of Mycobacterium tuberculosis, is inactivated by phosphorylation-dependent ClpC1P2 proteolysis. Mol. Microbiol.75:592-606.
4. An Efficient Method of Selectable Marker Gene Excision by Xer Recombination for Gene Replacement in Bacterial Chromosomes
5. Development of a repressible mycobacterial promoter system based on two transcriptional repressors
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