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. 1999 Jun;181(12):3751–3760. doi: 10.1128/jb.181.12.3751-3760.1999

FIG. 1.

FIG. 1

Anaerobic stability and O2 regulation of stability of the chromosomal nifHDKTY mRNA in the wild-type background and the pUX40 nifHDKTY mRNA in the ΔnifDK background. Representative Northern blots of RNA isolated after rifampin addition from chromosomal (UN) (panel 1) and ΔnifDK/pUX40 (UN5442) (panel 2) anaerobic cells derepressed for nif expression and from chromosomal (panel 3) and ΔnifDK/pUX40 (panel 4) cells treated with O2. Sampling times are indicated in minutes above the lanes. The time of O2 addition relative to sampling is indicated with a downward arrow above the indicated sampling times. A nifTY-specific probe was used in panels 1 and 2, and a nifKTY-specific probe was used in panels 3 and 4. Arrows a indicate nifHDKTY mRNA, and arrows b indicate nifHDK mRNA.