The results are presented as the difference in the average cycle threshold (ΔCt) with the control rpoD gene. Statistical

comparisons were performed by an anova and Tukey’s post-tests using prism 4.0 software (Graphpad Software). Total RNA (2.5 μg) Ruxolitinib cell line isolated from a culture of 2787 at an OD600 nm of 2.0 was converted to cDNA using the High-Capacity cDNA Reverse Transcription Kits (Applied Biosystems) according to the instructions of the manufacturer. PCR reactions were performed on the cDNA using the primers promo-R (5′-ACAATATGTTTCCTGACTCCTCAT-3′) and promo1-F (5′- ATTAGATTAACAAAAAGGATAACGTCAGATCT-3′), promo2-F (5′-CTTTTATTCGCCACGACACAAG-3′), promo3-F (5′-CCGTTCTAGTTATCTTGGATATTACATTAT-3′) or promo4-F (5′-TATTACATTATATAGGAGGGATTATGACTTTC-3′). The PCR amplification products were visualized on an agarose gel. RACE was performed using the 5′ RACE System, version 2.0 (Invitrogen), according to the instructions of the manufacturer with 3 μg of RNA extracted from E. coli 2787 grown to an OD600 nm this website of 0.7 or 2.0, with

gene-specific primers RACE_aah1 (5′-GGCTGGTTATCCGTATCGCC-3′), and RACE_aah2 (5′-CCAATTCTGTACGTTGCATAAGGC-3′) or RACE_aidA1 (5′-TGATATTTGTACTATCAGTTATACCTCCTG-3′ and RACE_aidA2 (5′AATCGTCTGATTTCCACCGC-3′). The amplified products were analyzed by agarose gel electrophoresis and sequenced. Samples of bacterial cultures were drawn at several times during growth and normalized at the same OD600 nm. The bacteria were pelleted and resuspended in 50 mM Tris-HCl, pH 7.5,

150 mM NaCl (TBS). Whole-cell samples were then diluted in twice-concentrated SDS-PAGE loading buffer Florfenicol containing β-mercaptoethanol, and denatured by heating at 100 °C for 10 min. The samples were then separated by SDS-PAGE on 10% acrylamide gels and transferred to polyvinylidene fluoride membranes (Millipore). Immunodetection was performed with a serum raised against glycosylated heat-extracted mature AIDA-I (Charbonneau et al., 2006) or antibodies against GroEL protein (Sigma). Immune complexes were revealed using secondary antibodies coupled to horseradish peroxidase and 3,3′,5,5′-tetramethylbenzidine (Sigma). Using primers extending upstream of aah and downstream of aidA, we completely sequenced the insert of plasmid pIB264 (Benz & Schmidt, 1989). The insert is 6241 nucleotides long, with a G+C content of 44.6% and the sequence has been deposited in GenBank (GU810159). The sequence upstream of aah reveals the 5′-end of an ORF (Fig. 1).