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  • 1
    ISSN: 1432-072X
    Keywords: Bacterial cell wall ; Crystalline surface layer (S-layer) ; Eubacterial glycoproteins ; Clostridium thermohydrosulfuricum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The location of the covalently attached carbohydrate residue of the S-layer glycoprotein from Clostridium thermohydrosulfuricum L111-69 was determined by electron microscopical procedures after converting the hydroxyl groups of the carbohydrate chains into carboxyl groups by succinylation. The introduction of carboxyl groups was examined by labelling with polycationized ferritin (PCF; a net positively charged topographical marker for electron microscopy). Cyanogen bromide was used for activating vicinal hydroxyl groups of the carbohydrate chains which could then react with amino groups of amino carbonic acids or ferritin. The amount of covalently bound ferritin was determined by freeze-etching and UV-measurement. Both, succinylation experiments and covalent attachment of ferritin confirmed that at least a considerable portion of the carbohydrate residue must be located on the S-layer surface.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-072X
    Keywords: Evolution ; Eubacteria ; Thermophile ; Anaerobe ; Thermotoga maritima
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A novel type of bacterium has been isolated from various geothermally heated locales on the sea floor. The organisms are strictly anaerobic, rod-shaped, fermentative, extremely thermophilic and grow between 55 and 90°C with an optimum of around 80°C. Cells show a unique sheath-like structure and monotrichous flagellation. By 16S rRNA sequencing they clearly belong to the eubacteria, although no close relationship to any known group could be detected. The majority of their lipids appear to be unique in structure among the eubacteria. Isolate MSB8 is described as Thermotoga maritima, representing the new genus Thermotoga.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-072X
    Keywords: Bacterial cell wall ; S-layer ; Crystalline surface layers ; Cell surface ; Glycoprotein ; Bacillaceae
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The structures, amino acid- and neutral sugar compositions of the crystalline surface layers (S-layers) of four selected strains each ofBacillus stearothermophilus andDesulfotomaculum nigrificans were compared. Among the four strains of each species a remarkable diversity in the molecular weights of the S-layer subunits and in the geometry and constants of the S-layer lattices was apparent. The crystalline arrays included hexagonal (p6), square (p4) and oblique (p2) lattices. In vitro self-assembly of isolated S-layer subunits (or S-layer fragments) led to the formation of flat sheets or open-ended cylindrical assembly products. The amino acid composition of the S-layers exhibited great similarities and was predominantly acidic. With the exception of the S-layers of two strains ofB. stearothermophilus (where only traces of neutral sugars could be detected), all other S-layer proteins seemed to be glycosylated. Among these strains significant differences in the amount and composition of the glycan portions were found. Based on this diversity interesting questions may be asked about the biological significance of the carbohydrate units of glycoproteins in prokaryotic organisms.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-072X
    Keywords: Methanogens ; Methanogenium liminatans spec. nov. ; 2-Propanol ; 2-Butanol ; Cyclopentanol ; S-layer ; Glycoprotein ; Polar lipids ; Polyamines
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A new mesophilic, coccoid methanogen, assigned as Methanogenium liminatans spec. nov. strain DSM 4140, was isolated from effluent of a reactor for the anaerobic treatment of industrial waste water. Cells of M. Liminatans formed irregular cocci, about 1.5 μm in size, and occurred singly. The cell envelope was an S-layer with hexagonally arranged glycoprotein subunits (Mr=118000). The center-to-center spacings were 15.4 nm. The polar lipid pattern was similar to that of Methanogenium tationis, the polyamine content similar to that found in several Methanogenium species. Strain DSM 4140 grew with H2/CO2, formate, 2-propanol/CO2, 2-butanol/CO2 and cyclopentanol/CO2. For growth with the different substrates acetate was required as an additional carbon source. Growth on H2/CO2 was stimulated by the addition of tungstate. The optimal concentration was 1–2 μM Na2WO4. 185WO inf4 sup2- was incorporated into cells. Growth was not influenced by 0–600 mM NaCl, but no growth occurred in the presence of ≥800 mM NaCl. Increasing concentrations of KCl up to 100 mM were slightly inhibitory for growth. The optimal growth temperature was around 40°C. The G+C content of the DNA was 59.3 mol% (Tm) or 60.5 mol% (HPLC).
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-072X
    Keywords: Crystalline surface layer ; S-layer ; Bacillaceae ; Lysozyme ; Mutanolysin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The structure of the S-layers from eight mesophilic Bacillaceae was investigated by freeze-etching of whole cells. The S-layer lattices from Bacillus alvei CCM 2051 and B. circulans CCM 1048 exhibited oblique symmetry. Square S-layer lattices were identified for B. polymyxa CCM 1459, B. circulans CCM 2048 and B. sphaericus strains CCM 2120 and CCM 2177. Two superimposed, structurally different S-layers were detected for B. brevis strains CCM 1089 and CCM 1463. In both organisms the outer S-layer lattice showed oblique and the inner S-layer lattice hexagonal symmetry. Labelling with polycationized ferritin (a net positively charged topographical marker for electron microscopy) revealed that the S-layer surface from all strains is not net negatively charged. In thin-section preparations all strains exhibited only a 5 nm thick peptidoglycan-containing layer. Whole cells from B. circulans CCM 2048 and from both B. brevis strains were rapidly lysed by the muramidases lysozyme (MW 14,600) and mutanolysine (MW 24,000) showing that their S-layers which allowed free passage for both enzymes must possess pores larger than 3.5 nm. By contrast, whole cells from B. circulans CCM 1048, B. alvei CCM 2051, B. polymyxa CCM 1459 and B. sphaericus strains CCM 2120 and CCM 2177 were resistant to both muramidases. It could be shown that these strains possess muramidase resistant peptidoglycan-containing layers. Therefore, the latter results did not confirm the claim in the literature that muramidase resistance of S-layer carrying mesophilic Bacillaceae is caused by the S-layer itself acting as a protective coat.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 156 (1991), S. 181-185 
    ISSN: 1432-072X
    Keywords: Bacterial cell wall ; S-layer ; Surface charge ; Surface hydrophobicity ; Bacterial adsorption ; Bacillus stearothermophilus
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Various aspects of surface properties of the S-layer-carrying Bacillus stearothermophilus PV72 and of an S-layer-deficient mutant (strain PV72/T5) have been tested by adsorption assays on solid surfaces, electrostatic interaction chromatography and hydrophobic interaction chromatography. The adsorption assays have shown that cell adhesion of the S-layer-carrying strain was less influenced by environmental changes than it was with the S-layer-deficient mutant. Electrostatic interaction chromatography indicated that both strains have positively and negatively charged groups exposed on the cell surface but the S-layer-carrying strain reveals more positively charged groups than does the S-layer-deficient mutant. Hydrophobic interaction chromatography showed that both strains have a hydrophilic surface but that the hydrophilic properties are more pronounced with the strain lacking an S-layer.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1432-072X
    Keywords: Bacterial cell wall ; S-layer ; Crystalline surface layers ; Surface charge ; Surface hydrophobicity ; Clostridium thermohydrosulfuricum ; Clostridium thermosaccharolyticum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Labelling experiments using a positively charged topographical marker for electron microscopy, polycationized ferritin, showed that the S-layers of two closely related clostridia Clostridium thermohydrosulfuricum L111-69 and C. thermosaccharolyticum D120-70 do not exhibit a net negative charge, as usually observed for bacterial cell surfaces. Chemical modification of reactive sites confirmed that amino and carboxyl groups are exposed on the S-layer surface of both strains. Amino-specific, bifunctional agents crosslinked both S-layer lattices. Studies with carbodiimides revealed that only the S-layer surface of C. thermohydrosulfuricum L111-69 had amino and carboxyl groups closely enough aligned to permit electrostatic interactions between the constituent protomers. The regular structure of this S-layer lattice was lost upon converting the carboxyl groups into neutral groups by amidation. Disintegration of both S-layer lattices occurred upon N-acetylation or N-succinylation of the free amino groups. Adhesion experiments showed that in neutral and weakly alkaline environment whole cells of C. thermosaccharolyticum D120-70 exhibited a stronger tendency to bind to charged surfaces than whole cells of C. thermohydrosulfuricum L111-69, but showed a lower tendency to bind to hydrophobic materials.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 149 (1988), S. 485-491 
    ISSN: 1432-072X
    Keywords: Crystalline cell surface layer ; S-layer ; Cell wall growth ; Bacillus stearothermophilus
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Bacillus stearothermophilus strains PV 72 and ATCC 12980 carry a crystalline surface layer (S-layer) with hexagonal (p6) and oblique (p2) symmetry, respectively. Sites of insertions of new subunits into the regular lattice during cell growth have been determined by the indirect fluorescent antibody technique and the protein A/colloidal gold technique. During S-layer growth on both bacillus strains the following common features were noted: 1. shedding of intact S-layer or turnover of individual subunits was not seen; 2. new S-layer was deposited in helically-arranged bands over the cylindrical surface of the cell at a pitch angle related to the orientation of the lattice vectors of the crystalline array; 3. little or no S-layer was inserted into pre-existing S-layer at the poles, and 4. septal regions and, subsequently, newly formed cell poles were covered with new S-layer protein.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    European biophysics journal 28 (1999), S. 583-590 
    ISSN: 1432-1017
    Keywords: Key words Crystalline bacterial surface layer ; S-layer ; Lipid membrane ; Irreversible breakdown
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Physics
    Notes: Abstract Isolated protein subunits of the crystalline bacterial cell surface layer (S-layer) of Bacillus coagulans E38-66 have been recrystallized on one side of planar black lipid membranes (BLMs) and their influence on the electrical properties, rupture kinetics and mechanical stability of the BLM was investigated. The effect on the boundary potential, the capacitance or the conductance of the membrane was negligible whereas the mechanical properties were considerably changed. The mechanical stability was characterized by applying voltage pulses or ramps to induce irreversible rupture. The amplitude of the voltage pulse leading to rupture allows conclusions on the ability of membranes to resist external forces. Surprisingly, these amplitudes were significantly lower for composite S-layer/lipid membranes compared to undecorated BLMs. In contrast, the delay time between the voltage pulse and the appearance of the initial defect was found to be drastically longer for the S-layer-supported lipid bilayer. Furthermore, the kinetics of the rupture process was recorded. Undecorated membranes show a fast linear increase of the pore conductance in time, indicating an inertia-limited defect growth. The attachment of an S-layer causes a slow exponential increase in the conductance during rupture, indicating a viscosity-determined widening of the pore. In addition, the mechanical properties on a longer time scale were investigated by applying a hydrostatic pressure across the BLMs. This causes the BLM to bulge, as monitored by an increase in capacitance. Compared to undecorated BLMs, a significantly higher pressure gradient has to be applied on the S-layer face of the composite BLMs to observe any change in capacitance.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    [s.l.] : Macmillan Magazines Ltd.
    Nature 389 (1997), S. 585-587 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Methods for organizing materials at the nanometre scale have advanced tremendously in recent years,. One important objective is the synthesis of patterned arrays of inorganic nanocrystals, whose optical, electronic and magnetic properties might find technological uses, for example as memory ...
    Type of Medium: Electronic Resource
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