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1.
Microbiology (Reading) ; 157(Pt 9): 2681-2693, 2011 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-21757492

RESUMO

Siderophores are high-affinity iron-chelating compounds produced by bacteria for iron uptake that can act as important virulence determinants for both plant and animal pathogens. Genome sequencing of the plant pathogen Streptomyces scabies 87-22 revealed the presence of a putative pyochelin biosynthetic gene cluster (PBGC). Liquid chromatography (LC)-MS analyses of culture supernatants of S. scabies mutants, in which expression of the cluster is upregulated and which lack a key biosynthetic gene from the cluster, indicated that pyochelin is a product of the PBGC. LC-MS comparisons with authentic standards on a homochiral stationary phase confirmed that pyochelin and not enantio-pyochelin (ent-pyochelin) is produced by S. scabies. Transcription of the S. scabies PBGC occurs via ~19 kb and ~3 kb operons and transcription of the ~19 kb operon is regulated by TetR- and AfsR-family proteins encoded by the cluster. This is the first report, to our knowledge, of pyochelin production by a Gram-positive bacterium; interestingly regulation of pyochelin production is distinct from characterized PBGCs in Gram-negative bacteria. Though pyochelin-mediated iron acquisition by Pseudomonas aeruginosa is important for virulence, in planta bioassays failed to demonstrate that pyochelin production by S. scabies is required for development of disease symptoms on excised potato tuber tissue or radish seedlings.


Assuntos
Fenóis/metabolismo , Proteínas Repressoras/metabolismo , Streptomyces/metabolismo , Tiazóis/metabolismo , Fatores de Transcrição/metabolismo , Vias Biossintéticas/genética , Regulação Bacteriana da Expressão Gênica , Ordem dos Genes , Modelos Biológicos , Família Multigênica , Plantas/metabolismo , Plantas/microbiologia , RNA Mensageiro , Raphanus/metabolismo , Raphanus/microbiologia , Proteínas Repressoras/genética , Solanum tuberosum/metabolismo , Solanum tuberosum/microbiologia , Streptomyces/genética , Fatores de Transcrição/genética , Transcrição Gênica
2.
Genome Biol ; 10(5): R51, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-19432983

RESUMO

BACKGROUND: Pseudomonas fluorescens are common soil bacteria that can improve plant health through nutrient cycling, pathogen antagonism and induction of plant defenses. The genome sequences of strains SBW25 and Pf0-1 were determined and compared to each other and with P. fluorescens Pf-5. A functional genomic in vivo expression technology (IVET) screen provided insight into genes used by P. fluorescens in its natural environment and an improved understanding of the ecological significance of diversity within this species. RESULTS: Comparisons of three P. fluorescens genomes (SBW25, Pf0-1, Pf-5) revealed considerable divergence: 61% of genes are shared, the majority located near the replication origin. Phylogenetic and average amino acid identity analyses showed a low overall relationship. A functional screen of SBW25 defined 125 plant-induced genes including a range of functions specific to the plant environment. Orthologues of 83 of these exist in Pf0-1 and Pf-5, with 73 shared by both strains. The P. fluorescens genomes carry numerous complex repetitive DNA sequences, some resembling Miniature Inverted-repeat Transposable Elements (MITEs). In SBW25, repeat density and distribution revealed 'repeat deserts' lacking repeats, covering approximately 40% of the genome. CONCLUSIONS: P. fluorescens genomes are highly diverse. Strain-specific regions around the replication terminus suggest genome compartmentalization. The genomic heterogeneity among the three strains is reminiscent of a species complex rather than a single species. That 42% of plant-inducible genes were not shared by all strains reinforces this conclusion and shows that ecological success requires specialized and core functions. The diversity also indicates the significant size of genetic information within the Pseudomonas pan genome.


Assuntos
Ecossistema , Genoma Bacteriano , Plantas/microbiologia , Pseudomonas fluorescens/genética , Plantas/metabolismo , Pseudomonas fluorescens/classificação , Pseudomonas fluorescens/metabolismo
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