Parameters related to lacZ expression from Pspc in strain SL106
Range | Table - link |
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Organism | Bacteria Escherichia coli |
Reference | Liang ST, Xu YC, Dennis P, Bremer H. mRNA composition and control of bacterial gene expression. J Bacteriol. 2000 Jun182(11):3037-44. p.3041 table 2PubMed ID10809680 |
Method | "Values are interpolated from observed data to match growth rate values in [Bremer, H., and P. P. Dennis. 1996. Modulation of chemical composition and other parameters of the cell by growth rate, p. 1553–1569. In F. C. Neidhardt, R. Curtiss III, J. L. Ingraham, E. C. C. Lin, K. B. Low, B. Magasanik, W. S. Reznikoff, M. Riley, M. Schaechter, and H. E. Umbarger (ed.), Escherichia coli and Salmonella: cellular and molecular biology, 2nd ed. ASM Press, Washington, D.C.], Tables 2 and 3" |
Comments | "In this report, [researchers] have considered the effects of bulk mRNA and free ribosomes on the synthesis of ß-galactosidase expressed from three artificial promoter-lacZ fusions carrying the promoters for the spc ribosomal protein operon (Pspc), the pBR322 plasmid replication inhibitor RNAI (PRNAI), and the pBR322 replication primer RNAII (PRNAII)." See notes beneath table |
Entered by | Uri M |
ID | 110061 |