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. 2005 May;11(5):728–738. doi: 10.1261/rna.7134305

TABLE 1.

L20Δ1 and L20Δ2 repress rpmI expression

Overproduced L20 β-Galactosidase activity (Miller units) Repression factor
None 102.8
Wild-type 1.67 61.6
L20Δ1 1.37 75.0
L20Δ2 1.17 87.9

The E. coli IBPC5311[λMQ21ΔNB] lysogen, carrying an rpml’-‘lacZ translational fusion, was transformed either with plasmid pBR322 or with plasmid pBL6ec expressing wild-type L20 and its two derivatives pBL6ecΔ6-20 and pBL6ecΔ6-29 expressing the L20Δ1 and L20Δ2 truncations, respectively. pBL6ec is a pBR322 derivative carrying rplT, which is constitutively expressed from a lac promoter and is not subjected to autogenous control. The repression factor is defined as the ratio of the β-galactosidase activity assayed in the presence of control plasmid pBR322 to the activity assayed in the presence of wild-type L20- or truncated L20-overproducing plasmid.