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Reclassification of the Specialized Metabolite Producer Pseudomonas mesoacidophila ATCC 31433 as a Member of the Burkholderia cepacia Complex.
Loveridge, E Joel; Jones, Cerith; Bull, Matthew J; Moody, Suzy C; Kahl, Malgorzata W; Khan, Zainab; Neilson, Louis; Tomeva, Marina; Adams, Sarah E; Wood, Andrew C; Rodriguez-Martin, Daniel; Pinel, Ingrid; Parkhill, Julian; Mahenthiralingam, Eshwar; Crosby, John.
Afiliação
  • Loveridge EJ; Department of Chemistry, Swansea University, Swansea, United Kingdom e.j.loveridge@swansea.ac.uk john.crosby@bristol.ac.uk.
  • Jones C; School of Chemistry, Cardiff University, Cardiff, United Kingdom.
  • Bull MJ; School of Biosciences, Cardiff University, Cardiff, United Kingdom.
  • Moody SC; School of Biosciences, Cardiff University, Cardiff, United Kingdom.
  • Kahl MW; Department of Biosciences, Swansea University, Swansea, United Kingdom.
  • Khan Z; School of Chemistry, Cardiff University, Cardiff, United Kingdom.
  • Neilson L; School of Chemistry, Cardiff University, Cardiff, United Kingdom.
  • Tomeva M; Department of Chemistry, Swansea University, Swansea, United Kingdom.
  • Adams SE; School of Medicine, Swansea University, Swansea, United Kingdom.
  • Wood AC; Department of Chemistry, Swansea University, Swansea, United Kingdom.
  • Rodriguez-Martin D; School of Medicine, Swansea University, Swansea, United Kingdom.
  • Pinel I; School of Chemistry, Cardiff University, Cardiff, United Kingdom.
  • Parkhill J; School of Chemistry, Cardiff University, Cardiff, United Kingdom.
  • Mahenthiralingam E; School of Chemistry, Cardiff University, Cardiff, United Kingdom.
  • Crosby J; School of Chemistry, Cardiff University, Cardiff, United Kingdom.
J Bacteriol ; 199(13)2017 07 01.
Article em En | MEDLINE | ID: mdl-28439036
Pseudomonas mesoacidophila ATCC 31433 is a Gram-negative bacterium, first isolated from Japanese soil samples, that produces the monobactam isosulfazecin and the ß-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.IMPORTANCE This work reports the complete genome sequence of Pseudomonas mesoacidophila ATCC 31433, a known producer of bioactive compounds. Large numbers of both known and novel biosynthetic gene clusters were identified, indicating that P. mesoacidophila ATCC 31433 is an untapped resource for discovery of novel bioactive compounds. Phylogenetic analysis demonstrated that P. mesoacidophila ATCC 31433 is in fact a member of the Burkholderia cepacia complex, most closely related to the species Burkholderia ubonensis Further investigation of the classification and biosynthetic potential of P. mesoacidophila ATCC 31433 is warranted.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pseudomonas / Complexo Burkholderia cepacia Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pseudomonas / Complexo Burkholderia cepacia Idioma: En Ano de publicação: 2017 Tipo de documento: Article