Effect of an Artificial RNA Marker on Gene Expression in Escherichia coli
Author:
Affiliation:
1. Department of Biology and Biochemistry
2. Department of Computer Science
3. Department of Chemical Engineering, University of Houston, Houston, Texas 77204-5001
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.71.7.4156-4159.2005
Reference27 articles.
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2. Ammons, D., J. Rampersad, and G. E. Fox. 1998. A genomically modified marker strain of Escherichia coli. Curr. Microbiol.37:341-346.
3. Ammons, D., J. Rampersad, and G. E. Fox. 1999. 5S rRNA gene deletions cause an unexpectedly high fitness loss in Escherichia coli. Nucleic Acids Res.27:637-642.
4. Amouyal, M., L. Mortensen, H. Buc, and K. Hammer. 1989. Single and double loop formation when deoR repressor binds to its natural operator sites. Cell58:545-551.
5. Arfin, S. M., A. D. Long, E. T. Ito, L. Tolleri, M. M. Riehle, E. S. Paegle, and G. W. Hatfield. 2000. Global gene expression profiling in Escherichia coli K12. The effects of integration host factor. J. Biol. Chem.275:29672-29684.
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