Figure 1 Alignment of E. coli AmpG, PA4218 and PA4393. The primary sequence of E. coli AmpG, PA4218 (AmpP) and PA4393 (AmpG) were used as an input to M-Coffee, which Entinostat solubility dmso combines multiple sequence alignments using the T-Coffee platform [45, 46]. Identical and similar amino

acids were shaded black and gray, respectively, using BOXSHADE. Analysis of the sequences around ampG and ampP revealed that they were in close proximity to two respective upstream ORFs. Based upon sequence analysis, it is likely that ampG and ampP constitute two two-gene operons with their respective upstream ORFs (Figures 2A and 2B). PA4219 (ampO) overlaps the first seven base pairs of ampP (Figure 2A). AmpO is a putative seven-transmembrane protein with a strong lipoprotein signal peptide that has a potential cleavage site between amino acids 18 and 19 [23]. The ampG gene is located 43 bp downstream from PA4392 (ampF), which encodes a putative protein with a DNA-protein cysteine methyltransferase domain (Figure 2B). The function of this domain remains unknown. PFT�� No lipoprotein signal was detected in AmpF. Figure 2 Physical

map of the ampO-ampP (A) and ampF-ampG (B) loci. The restriction map is based on PAO1 genome sequence with relevant restriction sites. (A) The 2779-bp ampO-ampP fragment has the PAO1 coordinates of 4721496 to 4724275. (B) The 2904-bp ampF-ampG fragment corresponds to the PAO1 coordinates of 4921591 to 4924494. The plasmids pKKF03 and pKKF04 are derivatives of pCRII-TOPO (Invitrogen, CA), whereas pKKF157 and pKKF161 are derivatives of pME6030 [41]. The Gm cassette (black Carbohydrate inverted triangle) was inserted into the HincII and AscI sites of pKKF03 and pKKF04, respectively. To determine if ampG and ampP constitute two-gene operons with their upstream ORFs, RNA isolated from PAO1 was analyzed by reverse transcription polymerase chain reaction (PCR) using

primers flanking the intergenic (ampF-ampG) (Figure 3A) and the overlapping (ampO-ampP) region (Figure 3B). The expected amplicon sizes are 136 and 158 bp for the ampF-G junction and ampO-P junction, respectively [23]. As expected, amplification was observed with genomic DNA (Figures 3A and 3B, Lane 3). In the RNA analyses, PCR products were observed in reverse transcription PCR when the template was prepared in the presence of reverse transcriptase (Figures 3A and 3B, Lane 1), but not in the control reaction when reverse transcriptase was omitted (Figures 3A and 3B, Lane 2). This confirms that ampO and ampP constitute a two-gene operon and ampF and ampG constitute another. In addition, reverse transcriptase real time PCR data is in agreement with ampO and ampP belonging to the same operon and ampF and ampG comprising another operon (data not shown). Figure 3 PCR analysis of ampFG and ampOP operon cDNA. Polyacrylamide gel electrophoresis of PCR products of the junctions of the ampOP and ampFG operons.