The integration of PFGI-1 probably is controlled by a phage-like tyrosine integrase encoded by PFL_4752 located 335 bp upstream from tRNALys. Figure 6 Organization of genomic island PFGI-1.

Predicted open reading frames are shaded according to their category and their orientation is shown by arrows. DNA regions unique to P. fluorescens Pf-5 and not found in closely related GIs from other Pseudomonas spp. are indicated by grey shading. Figure 7 Dot plot comparison of genomic island PFGI-1 with related genomic islands from other Pseudomonas spp. Sequences of GI from P. fluorescens Pf0-1 [GenBank acc. CP000094; locus tags Pfl_O1_2993 through Pfl_O1_R50], PPHGI-1 from P. syringae pv. phaseolicola 1302A Nirogacestat [33], GI-6 from P. syringae pv. syringae B728a [36], pKCL102 from P. aeruginosa C [30], PAPI-1 from P. aeruginosa UCBPP-PA14 [32], GI from P. aeruginosa PA7 [GenBank acc. CP000744; locus tags PSPA7_4437 through PSPA7_4531], ExoU-A island from P. aeruginosa 6077 [31], PAGI-2 and PAGI-4 from P. aeruginosa selleck screening library C [29], PAGI-3 from P. aeruginosa SGM17M [29], PAGI-5 from

P. aeruginosa PSE9 [GenBank acc. EF611301], and clc element from Pseudomonas sp. B13 [34] were concatenated and aligned with PFGI-1 using a dot plot function from OMIGA 2.0 with sliding window of 45 and hash value of 6. Lower panel shows a 500-bp sliding window plot of G+C content for PFGI-1 with dotted line tracing the average G+C content (63%) of Pf-5 genome. Genes involved in plasmid replication, recombination, conjugative transfer, and possible origin of PFGI-1 Whether PFGI-1 exists in strain Pf-5 or in any other Pseudomonas host as an episome is not known. However, the first two-thirds of PFGI-1 contain putative plasmid replication, partitioning and conjugation genes that are readily aligned at the DNA level with those from plasmid pKLC102 of P. aeruginosa C [30]. The putative origin of replication, oriV, is situated immediately upstream of PFL_4669

and spans about 1,100 bp. Plasmid origins of replication often contain arrays of specific ~20 bp repeats, called iterons, that serve as binding sites for the cognate replication initiator Rep protein and Dapagliflozin are involved in replication and partitioning [39, 40]. In addition to plasmid-specific iterons, some plasmid origins contain A+T-rich repeats where host replication initiation factors bind and open DNA, as well as repeats serving as binding sites for the host DnaA initiator protein. The putative oriV from PFGI-1 exhibits typical features of a plasmid replication origin. The first half is A+T-rich and has four conserved https://www.selleckchem.com/products/MDV3100.html direct repeats of a perfect 23-bp palindrome (5′-CTGAGTTCGGAATCCGAACTCAGT-3′). The second half is represented by a G+C-rich stretch that overlaps with the region between PFL_4668 and PFL_4669 and contains four conserved 46-bp direct repeats, each of which includes an imperfect 21-bp inverted repeat (5′-AGTGTTGTGGGCCACACCACT-3′).

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