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1.
Genome Announc ; 5(11)2017 Mar 16.
Article in English | MEDLINE | ID: mdl-28302790

ABSTRACT

This paper describes the complete genome sequences and methylome analysis of six psychrotrophic strains isolated from perennially ice-covered Lake Untersee in Antarctica.

2.
Carbohydr Res ; 381: 138-41, 2013 Nov 15.
Article in English | MEDLINE | ID: mdl-24096274

ABSTRACT

The O-polysaccharide isolated by mild acid hydrolysis of the lipopolysaccharide of Pseudomonas mandelii CYar1 was studied by sugar analysis and 1D and 2D (1)H and (13)C NMR spectroscopies. The following structure of the O-polysaccharide was established:


Subject(s)
Deoxy Sugars/chemistry , Oligosaccharides/chemistry , Polysaccharides/chemistry , Pseudomonas/chemistry , Carbohydrate Conformation , Hydrolysis , Magnetic Resonance Spectroscopy , Polysaccharides/isolation & purification
3.
Int J Syst Evol Microbiol ; 62(Pt 1): 33-37, 2012 Jan.
Article in English | MEDLINE | ID: mdl-21317277

ABSTRACT

A psychrotolerant sulfate-reducing bacterium, designated B15(T), was isolated from supercooled water brine from within permafrost of the Varandey Peninsula, on the southern coast of the Barents Sea. Cells were Gram-negative, motile vibrions (3.0-4.0×0.4-0.5 µm) with a single polar flagellum. The isolate was positive for desulfoviridin as a bisulfite reductase. Strain B15(T) grew at -2 to 28 °C (optimum 24 °C) and with 0-2.0% NaCl (optimum 0.2%). The isolate used H(2) plus acetate, formate, ethanol, lactate, pyruvate and choline as electron donors and used sulfate, sulfite, thiosulfate, elemental sulfur, DMSO and Fe(3+) as electron acceptors. Pyruvate and lactate were not fermented in the absence of sulfate. The G+C content of genomic DNA was 55.2 mol%. Analysis of the 16S rRNA gene sequence showed that the isolate belonged to the genus Desulfovibrio. Its closest relatives were Desulfovibrio idahonensis CY1(T) (98.8% 16S rRNA gene sequence similarity) and Desulfovibrio mexicanus Lup1(T) (96.5%). On the basis of genotypic, phenotypic and phylogenetic characteristics, the isolate represents a novel species, for which the name Desulfovibrio arcticus sp. nov. is proposed; the type strain is B15(T) (=VKM B-2367(T)=DSM 21064(T)).


Subject(s)
Desulfovibrio/classification , Desulfovibrio/isolation & purification , Environmental Microbiology , Sulfates/metabolism , Bacterial Typing Techniques , Base Composition , Cluster Analysis , DNA, Bacterial/chemistry , DNA, Bacterial/genetics , DNA, Ribosomal/chemistry , DNA, Ribosomal/genetics , Desulfovibrio/genetics , Desulfovibrio/physiology , Flagella/physiology , Hydrogensulfite Reductase/analysis , Molecular Sequence Data , Oxidation-Reduction , Phylogeny , RNA, Ribosomal, 16S/genetics , Sequence Analysis, DNA , Sodium Chloride/metabolism , Temperature
4.
FEMS Microbiol Ecol ; 69(2): 180-93, 2009 Aug.
Article in English | MEDLINE | ID: mdl-19486154

ABSTRACT

Two strains (NF1 and NF3) of free-living chemoorganotrophic bacteria have been isolated from multiyear oil slime and Pedilanthus tithymaloides rhizosphere and ascribed to the genus Kaistia of the class Alphaproteobacteria on the basis of the nucleotide sequences of 16S rRNA gene and phenotypic characteristics. These strains can be assigned to ultramicrobacteria as their populations are represented by two subpopulations: (1) ultrasmall cells, on average 200-300 nm in diameter and <0.1 microm(3) in volume, of up to 60% of the total number of cells in a population, and (2) cells 400-800 nm in diameter and 0.15-0.5 microm(3) in volume, of up to 40% of the total number of cells in a population. The interaction of the isolated ultramicrobacteria strains (IUMB) with different bacterial species has been studied in cocultures grown under starvation and in complete nutrient media. It has been found that IUMB can be facultative parasites on certain species of chemoorganotrophic and phototrophic bacteria. The interaction of IUMB with prey bacteria exhibits the extracellular type of parasitism and involves establishing stable cell-cell contacts between the parasites and their prey to cause destruction of host cells.


Subject(s)
Rhizobiaceae/isolation & purification , Rhizobiaceae/physiology , Soil Microbiology , Culture Media , Gram-Negative Bacteria/growth & development , Gram-Positive Bacteria/growth & development , Microscopy, Electron , RNA, Bacterial/genetics , RNA, Ribosomal, 16S/genetics , Rhizobiaceae/genetics , Rhizobiaceae/ultrastructure
5.
J Invertebr Pathol ; 88(1): 17-26, 2005 Jan.
Article in English | MEDLINE | ID: mdl-15707865

ABSTRACT

Parasitic bacteria of the genus Pasteuria are reported for three Anaplectus and four identified and several unidentified Plectus species found in eight countries in various habitats. The pasteurias from plectids agree in essential morphological characters of sporangia and endospores as well as in developmental cycle with those of the Pasteuria species and strains described from tylenchid nematodes, but appear to be mainly distinguished from these by absence of a distinct perisporium in the spores and the endospores obviously not being cup- or saucer-shaped. The wide range of measurements and morphological peculiarities of sporangia and endospores suggest that probably several Pasteuria species have to be distinguished as parasites in Plectidae. From an infected juvenile of an unidentified plectid species the 16S rRNA gene sequence of Pasteuria sp. was obtained. Substantial sequence divergence from described Pasteuria species and its phylogenetic position on molecular trees indicate that this Pasteuria sp. could be considered as a new species. Preliminary results of the analysis of DNA phylogeny of Pasteuria spp. and their nematode hosts provide evidence for incongruence of their phylogenetic history and of host switching events during evolution of the bacterial parasites.


Subject(s)
Bacterial Physiological Phenomena , Gram-Positive Endospore-Forming Bacteria/classification , Gram-Positive Endospore-Forming Bacteria/physiology , Nematoda/parasitology , Animals , Base Sequence , DNA, Bacterial/analysis , Host-Parasite Interactions , Molecular Sequence Data , Phylogeny , Polymerase Chain Reaction , RNA, Ribosomal, 16S/genetics
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