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. 1999 Oct;181(19):6042–6052. doi: 10.1128/jb.181.19.6042-6052.1999

FIG. 6.

FIG. 6

(A) β-Galactosidase assays of E. carotovora subsp. carotovora AC5047 or its RsmC mutant AC5050 carrying the cloning vector pNM481Spr, pAKC887 (rsmAEcc-lacZ fusion), pAKC888 (rsmAEa-lacZ fusion), pAKC889 (rsmAEhg-lacZ fusion), and pAKC890 (csrA-lacZ fusion). Bacteria were grown at 28°C in minimal salts medium plus sucrose and spectinomycin to an A600 of 2.0 and assayed for β-galactosidase activity. (B) β-Galactosidase assays of E. carotovora subsp. carotovora AC5047 or its RsmC mutant AC5050 carrying the cloning vector pMP220 or the rsmB-lacZ plasmid pAKC1002. Bacteria were grown at 28°C in minimal salts medium plus sucrose and tetracycline to an A600 of 2.0 and assayed for β-galactosidase activity.