Complete genome sequence of Pseudomonas aeruginosa PAO1, an opportunistic pathogen

By C. Stover, X. Pham, A. Erwin, S. Mizoguchi, P. Warrener, M. Hickey, Fiona S. L. Brinkman, W. O. Hufnagle, D. J. Kowalik, Lagrou Mj and 21 more. Nature, 2000

4,461 citations recorded by the source corpus.

Subfields: Molecular Biology, Molecular Medicine

View Paper: https://www.semanticscholar.org/paper/a1bd75dac9a95574a75f4ac0ff1b8de487744b74

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Citations in the corpus

Genomic analysis reveals that Pseudomonas aeruginosa virulence is combinatorial (2006, methodology): “Genome Biology 2006, 7:R90 PAO1-like arrangement of genome sequence between the two most distant copies of a large ribosomal RNA cluster (Figures 1 and 2a,b; also see Stover and coworkers [ 7 ]).”
Microarray-Based Analysis of the Staphylococcus aureus σB Regulon (2004, background): “... six alternative factors are produced by the enteric bacterium Escherichia coli (reviewed in reference 6). Genomic sequence analysis suggests that many alternative factors also exist in a number of other pathogenic species such as Treponema palladium (4 alternative factors) (21), Vibro cholerae (”
Metabolic-network-driven analysis of bacterial ecological strategies (2009, background): “The negative correlation between ESI and duplication time is also maintained in species that are evenly distributed among different habitat types and taxonomic groups (Additional data file 3). Pseudomonas aeruginosa, an organism with a high ESI score (Additional data file 1) provides an example of f”
A Type VI Secretion System of Pseudomonas aeruginosa Targets a Toxin to Bacteria (2010, neutral): “Tsi2 Is an Essential Protein that Protects P. aeruginosa from Tse2 The lack of transposon insertions within the tse2/tsi2 locus in a published transposon insertion library of P. aeruginosa PAO1 suggested that these ORFs may be essential for viability of the organism (Jacobs et al., 2003).”
BIOSYNTHESIS OF ANTIBIOTICS BY PGPR AND ITS RELATION IN BIOCONTROL OF PLANT DISEASES (2005, background): “The results thus provide evidence that production of CLPs is habitat specific (produced specifically in rhizosphere) 82 Fernando et al. rather than in the bulk soil, where the rate of degradation is faster (Nielsen et al., 2002).”
Mechanisms of biocontrol and plant growth-promoting activity in soil bacterial species of Bacillus and Pseudomonas: a review (2012, background): “…may have insecticidal activity (Péchy-Tarr et al. 2008; Pardo-López et al. 2009), while some Pseudomonas species may be pathogenic to humans (Stover et al. 2000); they may even be important in other areas, such as biotechnology and bioremediation (Rehman, Butt, and Hasnain 2010), although…”
Molecular basis of bacterial resistance to chloramphenicol and florfenicol. (2004, background): “The catB7 genes – representing group B-4 – were found in the chromosome of P. aeruginosa PAO222 [114] and PAO1 [115] whereas catB9 genes – representing group B-5 – were found in the chromosomal DNA of Vibrio cholerae [116,117] as part of a super-integron [116].”
Non‐coding RNAs: the architects of eukaryotic complexity (2001, background): “The fruitfly Drosophila melanogaster and the nematode Caenorhabditis elegans appear to have only about twice as many protein coding genes (∼12–14 000) as microorganisms such as Saccharomyces cerevisiae (∼6200) and Pseudomonas aeruginosa (∼5500) (Rubin et al., 2000; Stover et al., 2000).”