Summary
The guaB gene is the first gene in GMP biosynthesis. It harbours a potential DnaA protein binding site (dnaA box, 5’-TTATCCACA) in its coding region. This box is in the active orientation for DnaA-mediated transcription termination. The location of the guaB promoter was defined using a promoter search plasmid with galK as a monitoring gene. Transcription originating at the promoter and entering the gene was quantified under varying levels of DnaA protein. The formation of the DnaA protein/dnaA box complex in the coding region of guaB resulted in a decrease in guaB expression due to transcription termination. DnaA protein, therefore, represents a regulatory element in guaB expression.
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© 1992 Springer-Verlag Berlin Heidelberg
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Schaefer, C., Holz, A., Messer, W. (1992). DnaA Protein Mediated Transcription Termination in the GUA Operon of Escherichia coli . In: Hughes, P., Fanning, E., Kohiyama, M. (eds) DNA Replication: The Regulatory Mechanisms. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-76988-7_15
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DOI: https://doi.org/10.1007/978-3-642-76988-7_15
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