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. Author manuscript; available in PMC: 2010 May 8.
Published in final edited form as: J Mol Biol. 2009 Mar 14;388(3):415–430. doi: 10.1016/j.jmb.2009.03.023

Table 1.

Effects of DIP and DEC on colony size and determination of the half-life of wild type and variant Rob proteins

Addition to lactose tetrazolium plates containing 0.2% or 2% arabinose
No treatment
DIP (1 mM)
DEC (3 mM)
Rob Allele Representative Western Blot Half-life 0.2% 2% 0.2% 2% 0.2% 2%
None normal normal normal normal normal normal
Wild type graphic file with name nihms117122t1.jpg >20 hr normal normal SMALL NO GROWTH SMALL NO GROWTH
RobR40A graphic file with name nihms117122t2.jpg >20 hr normal normal normal normal normal normal
Rob107 graphic file with name nihms117122t3.jpg <1 min normal normal normal normal normal normal
Rob249 graphic file with name nihms117122t4.jpg 20 min normal SMALL normal SMALL normal SMALL
SoxS-Rob graphic file with name nihms117122t5.jpg >20 hr normal normal NO GROWTH NO GROWTH NO GROWTH NO GROWTH
SoxS 2 min normal normal normal normal normal normal

Overnight cultures of strain RA4468 [pBAD18-Rob] carrying different rob alleles were diluted10−6 and 0.1 ml plated on lactose tetrazolium plates with 0.2% or 2% arabinose along with DIP (1 mM), or DEC (3 mM). Growth phenotypes were determined after incubating the plates at 37°C for 15 hr. In separate experiments, the half-life of the respective proteins was determined by western blotting. The half-life of native SoxS27 was determined previously and the value is included here.