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1.
Astrobiology ; 13(1): 57-67, 2013 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-23276206

RESUMO

Opaline silica was detected, with Raman spectroscopy, in carbonaceous microfossils (especially Myxococcoides) in silicified filamentous microbial mats within dolomitized conglomerates of the Draken Formation (-800 to -700 Ma). High-resolution electron microscopy (HRTEM) and microprobe analyses were used to confirm the nature of this phase in the quartz matrix of the microbial mats. The silica likely precipitated in a microcrystalline form onto the organic macromolecules around, and within, the degrading microorganisms and preserved them by inhibiting the natural phase change to quartz. The Raman signal of opaline silica associated with carbonaceous matter and other biosignatures could be a potential indicator of biogenicity. This kind of association could be very useful during the future ExoMars mission (ESA/Roscosmos, 2018) that will search for traces of past life on Mars.


Assuntos
Carbono/química , Fósseis , Sedimentos Geológicos/química , Sedimentos Geológicos/microbiologia , Dióxido de Silício/química , Myxococcus/ultraestrutura , Noruega , Quartzo/química , Análise Espectral Raman
2.
Curr Biol ; 12(5): 369-77, 2002 Mar 05.
Artigo em Inglês | MEDLINE | ID: mdl-11882287

RESUMO

BACKGROUND: Many microorganisms, including myxobacteria, cyanobacteria, and flexibacteria, move by gliding. Although gliding always describes a slow surface-associated translocation in the direction of the cell's long axis, it can result from two very different propulsion mechanisms: social (S) motility and adventurous (A) motility. The force for S motility is generated by retraction of type 4 pili. A motility may be associated with the extrusion of slime, but evidence has been lacking, and how force might be generated has remained an enigma. Recently, nozzle-like structures were discovered in cyanobacteria from which slime emanated at the same rate at which the bacteria moved. This strongly implicates slime extrusion as a propulsion mechanism for gliding. RESULTS: Here we show that similar but smaller nozzle-like structures are found in Myxococcus xanthus and that they are clustered at both cell poles, where one might expect propulsive organelles. Furthermore, light and electron microscopical observations show that slime is secreted in ribbons from the ends of cells. To test whether the slime propulsion hypothesis is physically reasonable, we construct a mathematical model of the slime nozzle to see if it can generate a force sufficient to propel M. xanthus at the observed velocities. The model assumes that the hydration of slime, a cationic polyelectrolyte, is the force-generating mechanism. CONCLUSIONS: The discovery of nozzle-like organelles in various gliding bacteria suggests their role in prokaryotic gliding. Our calculations and our observations of slime trails demonstrate that slime extrusion from such nozzles can account for most of the observed properties of A motile gliding.


Assuntos
Myxococcus/fisiologia , Cianobactérias/fisiologia , Cianobactérias/ultraestrutura , Microscopia Eletrônica , Modelos Biológicos , Movimento , Muco/fisiologia , Myxococcus/ultraestrutura , Organelas/fisiologia , Organelas/ultraestrutura
3.
J Bacteriol ; 179(4): 1246-52, 1997 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-9023208

RESUMO

For the first time, chain-like aggregates, called "strands," have been enriched from crude cell wall preparations of liquid-grown vegetative cells of two strains of Myxococcus xanthus. These strands are highly isomorphic to macromolecular structures, previously described for Myxococcus fulvus (Lünsdorf and Reichenbach, J. Gen. Microbiol. 135:1633-1641, 1989). The strands are morphologically composed of ring elements, consisting of six or more peripheral protein masses and possibly three small central masses. The ring elements are linked by two parallel strings of filamentous proteins, called elongated elements, which keep the ring elements at a constant distance. The overall dimensions of the ring elements are 16.6 +/- 1.0 nm (n = 55) for M. xanthus Mx x48 and 16.4 +/- 1.5 nm (n = 37) for M. xanthus DK 1622. The distance between the ring elements, as a measure of the length of the elongated elements, is 16.6 +/- 1.1 nm (n = 59) for strain Mx x48 and 15.5 +/- 0.6 nm (n = 41) for strain DK 1622. Characteristically, the strands and oligomeric forms thereof show a strict association with the outer membrane. In situ studies of freeze-fractured cells of M. fulvus showed ring elements, isomorphic to those described for M. xanthus, within the periplasm; they appeared in parallel rows just below the outer membrane but not in direct contact with the cytoplasmic membrane. A three-dimensional model summarizes the morphological data. It is hypothesized that the chain-like strands, as building blocks of a more complex belt-like continuum, represent the peripheral part of the gliding machinery, which transforms membrane potential energy into mechanical work.


Assuntos
Myxococcus xanthus/ultraestrutura , Myxococcus/ultraestrutura , Proteínas de Bactérias/análise , Fracionamento Celular , Membrana Celular/química , Membrana Celular/ultraestrutura , Parede Celular/química , Parede Celular/ultraestrutura , Eletroforese em Gel de Poliacrilamida , Técnica de Fratura por Congelamento , Lipopolissacarídeos/análise , Microscopia Eletrônica , Movimento , Myxococcus/química , Myxococcus/fisiologia , Myxococcus xanthus/química , Myxococcus xanthus/fisiologia , Peptídeos/análise
4.
New Microbiol ; 18(4): 399-407, 1995 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-8590393

RESUMO

Twelve monoclonal antibodies (mAbs) directed against cell-surface antigens of Myxococcus virescens cells were developed and partially characterized. All of them recognized multiple, diffuse proteic bands in Western blot and four were also reactive to living bacteria, as assessed by flow cytometry. The four latter mAbs recognized antigens common to a number of vegetative forms and spores. The selective expression of proteins recognized by mAbs on the microorganisms and the possible applications of mAbs to the study of myxobacterial cell interaction are discussed.


Assuntos
Anticorpos Monoclonais , Antígenos de Bactérias , Antígenos de Superfície , Myxococcus/imunologia , Anticorpos Antibacterianos , Especificidade de Anticorpos , Proteínas de Bactérias/imunologia , Microscopia Imunoeletrônica , Myxococcus/crescimento & desenvolvimento , Myxococcus/ultraestrutura , Esporos Bacterianos/imunologia
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