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1.
Int J Syst Evol Microbiol ; 70(4): 2440-2448, 2020 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-32100697

RESUMEN

Pectobacterium strains isolated from potato stems in Finland, Poland and the Netherlands were subjected to polyphasic analyses to characterize their genomic and phenotypic features. Phylogenetic analysis based on 382 core proteins showed that the isolates clustered closest to Pectobacterium polaris but could be divided into two clades. Average nucleotide identity (ANI) analysis revealed that the isolates in one of the clades included the P. polaris type strain, whereas the second clade was at the border of the species P. polaris with a 96 % ANI value. In silico genome-to-genome comparisons between the isolates revealed values below 70%, patristic distances based on 1294 core proteins were at the level observed between closely related Pectobacterium species, and the two groups of bacteria differed in genome size, G+C content and results of amplified fragment length polymorphism and Biolog analyses. Comparisons between the genomes revealed that the isolates of the atypical group contained SPI-1-type Type III secretion island and genes coding for proteins known for toxic effects on nematodes or insects, and lacked many genes coding for previously characterized virulence determinants affecting rotting of plant tissue by soft rot bacteria. Furthermore, the atypical isolates could be differentiated from P. polaris by their low virulence, production of antibacterial metabolites and a citrate-negative phenotype. Based on the results of a polyphasic approach including genome-to-genome comparisons, biochemical and virulence assays, presented in this report, we propose delineation of the atypical isolates as a novel species Pectobacterium parvum, for which the isolate s0421T (CFBP 8630T=LMG 30828T) is suggested as a type strain.


Asunto(s)
Pectobacterium/clasificación , Filogenia , Solanum tuberosum/microbiología , Sistemas de Secreción Tipo III , Análisis del Polimorfismo de Longitud de Fragmentos Amplificados , Técnicas de Tipificación Bacteriana , Composición de Base , ADN Bacteriano/genética , Finlandia , Países Bajos , Pectobacterium/aislamiento & purificación , Enfermedades de las Plantas/microbiología , Tallos de la Planta/microbiología , Polonia , ARN Ribosómico 16S/genética , Análisis de Secuencia de ADN , Virulencia
2.
ISME J ; 13(5): 1198-1208, 2019 05.
Artículo en Inglés | MEDLINE | ID: mdl-30643197

RESUMEN

The Black Sea is the world's largest anoxic basin and a model system for studying processes across redox gradients. In between the oxic surface and the deeper sulfidic waters there is an unusually broad layer of 10-40 m, where neither oxygen nor sulfide are detectable. In this suboxic zone, dissolved phosphate profiles display a pronounced minimum at the upper and a maximum at the lower boundary, with a peak of particulate phosphorus in between, which was suggested to be caused by the sorption of phosphate on sinking particles of metal oxides. Here we show that bacterial polyphosphate inclusions within large magnetotactic bacteria related to the genus Magnetococcus contribute substantially to the observed phosphorus peak, as they contain 26-34% phosphorus compared to only 1-5% in metal-rich particles. Furthermore, we found increased gene expression for polyphosphate kinases by several groups of bacteria including Magnetococcaceae at the phosphate maximum, indicating active bacterial polyphosphate degradation. We propose that large magnetotactic bacteria shuttle up and down within the suboxic zone, scavenging phosphate at the upper and releasing it at the lower boundary. In contrast to a passive transport via metal oxides, this bacterial transport can quantitatively explain the observed phosphate profiles.


Asunto(s)
Alphaproteobacteria/metabolismo , Polifosfatos/metabolismo , Agua de Mar/química , Agua de Mar/microbiología , Alphaproteobacteria/genética , Mar Negro , Fenómenos Magnéticos , Fosfatos/análisis , Fósforo/análisis , Fosfotransferasas (Aceptor del Grupo Fosfato)/genética , Fosfotransferasas (Aceptor del Grupo Fosfato)/metabolismo
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