Table 1.
Antibiogram assay.
Table 2.
MIC and MBEC assays with different Pseudomonas putida strains.
Figure 1.
Genetic organization of pPC9, in white, genes forming the backbone of pPC9, in grey genes from the insert with homology to genes related to transposition, in black genes from the insert with antibiotic resistance function.
Figure 2.
Genetic organization of the pPC9 “insert.”
Black arrows represent genes with functions related to antibiotic resistance. In grey are genes with functions related to transposition and insertion machinery. Non-colored genes are those that encode hypothetical proteins, those with unknown function, or those with functions unrelated to antibiotic resistance, transposition or integration. Horizontal lines over genes represent DNA homology to different microorganisms, and percentages indicate the degree of homology.
Figure 3.
Location of the antibiotic and solvent efflux ttgGHI pumps within a genomic island in the chromosome of strain HB3267.
ttgGHI efflux genes are indicated in black; genes involved in transposition events are in light grey; the cbz operon, which is involved in chlorobenzene degradation, is in medium grey. Vertical lines indicate the insertion point; arrows above the sequence indicate the inverted repeat sequences of the Tn552-like transposon, which are within the magnesium chelatase.
Figure 4.
Potential chromosomal determinants for chloramphenicol resistance of HB3267.
(A) In black, chromosomal location of the additional pqqC gene of HB3267.; in grey, the region of the HB3267 chromosome that is not present in KT2440; in white, genes in synteny with KT2440. (B) Protein alignment of AgmR from P. putida HB3267 (HB3267, Locus B479_11475), P. putida S16 (S16, PPS_2213), P. putida KT2440 (PPS_2213, PP_2665), P. putida BIRD-1 (BIRD1, PPUBIRD1_3011), P. putida GB-1 (GB1, PputGB1_3138), P. aeruginosa PA7 (PA7, PSPA7_3317), and P. aeruginosa PAO1 (PAO1, PA1978) strains. Amino acid mutations referred to in the text are indicated in bold.