Reclassification of the specialized metabolite producer Pseudomonas mesoacidophila ATCC 31433 as a member of the Burkholderia cepacia complex
Pseudomonas mesoacidophila ATCC 31433 is a Gram-negative bacterium, first isolated from Japanese soil samples, that produces the monobactam isosulfazecin and the β-lactam-potentiating bulgecins. To characterize the biosynthetic potential of P. mesoacidophila ATCC 31433, its complete genome was determined using single-molecule real-time DNA sequence analysis. The 7.8-Mb genome comprised four replicons, three chromosomal (each encoding rRNA) and one plasmid. Phylogenetic analysis demonstrated that P. mesoacidophila ATCC 31433 was misclassified at the time of its deposition and is a member of the Burkholderia cepacia complex, most closely related to Burkholderia ubonensis. The sequenced genome shows considerable additional biosynthetic potential; known gene clusters for malleilactone, ornibactin, isosulfazecin, alkylhydroxyquinoline, and pyrrolnitrin biosynthesis and several uncharacterized biosynthetic gene clusters for polyketides, nonribosomal peptides, and other metabolites were identified. Furthermore, P. mesoacidophila ATCC 31433 harbors many genes associated with environmental resilience and antibiotic resistance and was resistant to a range of antibiotics and metal ions. In summary, this bioactive strain should be designated B. cepacia complex strain ATCC 31433, pending further detailed taxonomic characterization. © 2017 American Society for Microbiology.
Autores principales: | Loveridge, E. J., Jones, C., Bull, M. J., Moody, S. C., Kahl, M. W., Khan, Z., Neilson, L., Tomeva, M., Adams, S. E., Wood, A. C., Rodriguez-Martin, D., Pinel, I., Parkhill, J., Mahenthiralingam, E., Crosby, J. |
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Formato: | journal article biblioteca |
Idioma: | English |
Publicado: |
American Society for Microbiology
2017
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Materias: | Genome, Identification, Antibiotic resistance, Metal resistance, Antibacterial, Biosynthesis, Bulgecin, |
Acceso en línea: | http://hdl.handle.net/20.500.12792/2524 http://hdl.handle.net/10261/293365 |
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