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| 2. |
- Coenen, J. W., et al.
(författare)
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Transient induced tungsten melting at the Joint European Torus (JET)
- 2017
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Ingår i: Physica Scripta. - : IOP PUBLISHING LTD. - 0031-8949 .- 1402-4896. ; T170
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Tidskriftsartikel (refereegranskat)abstract
- Melting is one of the major risks associated with tungsten (W) plasma-facing components (PFCs) in tokamaks like JET or ITER. These components are designed such that leading edges and hence excessive plasma heat loads deposited at near normal incidence are avoided. Due to the high stored energies in ITER discharges, shallow surface melting can occur under insufficiently mitigated plasma disruption and so-called edge localised modes-power load transients. A dedicated program was carried out at the JET to study the physics and consequences of W transient melting. Following initial exposures in 2013 (ILW-1) of a W-lamella with leading edge, new experiments have been performed on a sloped surface (15 degrees slope) during the 2015/2016 (ILW-3) campaign. This new experiment allows significantly improved infrared thermography measurements and thus resolved important issue of power loading in the context of the previous leading edge exposures. The new lamella was monitored by local diagnostics: spectroscopy, thermography and high-resolution photography in between discharges. No impact on the main plasma was observed despite a strong increase of the local W source consistent with evaporation. In contrast to the earlier exposure, no droplet emission was observed from the sloped surface. Topological modifications resulting from the melting are clearly visible between discharges on the photographic images. Melt damage can be clearly linked to the infrared measurements: the emissivity drops in zones where melting occurs. In comparison with the previous leading edge experiment, no runaway melt motion is observed, consistent with the hypothesis that the escape of thermionic electrons emitted from the melt zone is largely suppressed in this geometry, where the magnetic field intersects the surface at lower angles than in the case of perpendicular impact on a leading edge. Utilising both exposures allows us to further test the model of the forces driving melt motion that successfully reproduced the findings from the original leading edge exposure. Since the ILW-1 experiments, the exposed misaligned lamella has now been retrieved from the JET machine and post mortem analysis has been performed. No obvious mass loss is observed. Profilometry of the ILW-1 lamella shows the structure of the melt damage which is in line with the modell predictions thus allowing further model validation. Nuclear reaction analysis shows a tenfold reduction in surface deuterium concentration in the molten surface in comparison to the non-molten part of the lamella.
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| 3. |
- Hood, D W, et al.
(författare)
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Biosynthesis of cryptic lipopolysaccharide glycoforms in Haemophilus influenzae involves a mechanism similar to that required for O-antigen synthesis
- 2004
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Ingår i: Journal of Bacteriology. - 0021-9193 .- 1098-5530. ; 186:21, s. 7429-7439
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Tidskriftsartikel (refereegranskat)abstract
- It is generally thought that mucosal bacterial pathogens of the genera Haemophilus, Neisseria, and Moraxella elaborate lipopolysaccharide (LPS) that is fundamentally different from that of enteric organisms that express O-specific polysaccharide side chains. Haemophilus influenzae elaborates short-chain LPS that has a role in the pathogenesis of H. influenzae infections. We show that the synthesis of LPS in this organism can no longer be as clearly distinguished from that in other gram-negative bacteria that express an O antigen. We provide evidence that a region of the H. influenzae genome, the hmg locus, is involved in the synthesis of glycoforms in which tetrasaccharide units are added en bloc, not stepwise, to the normal core glycoforms, similar to the biosynthesis of an O-antigen.
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| 4. |
- Hood, Derek W., et al.
(författare)
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Genes required for the synthesis of heptose-containing oligosaccharide outer core extensions in Haemophilus influenzae lipopolysaccharide
- 2010
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Ingår i: Microbiology. - : Microbiology Society. - 1350-0872 .- 1465-2080. ; 156, s. 3421-3431
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Tidskriftsartikel (refereegranskat)abstract
- Heptose-containing oligosaccharides (OSs) are found in the outer core of the lipopolysaccharide (LPS) of a subset of non-typable Haemophilus influenzae (NTHi) strains. Candidate genes for the addition of either L-glycero-D-manno-heptose (LD-Hep) or D-glycero-D-manno-heptose (DD-Hep) and subsequent hexose sugars to these OSs have been identified from the recently completed genome sequences available for NTHi strains. losA1/losB1 and losA2/losB2 are two sets of related genes in which losA has homology to genes encoding glycosyltransferases and losB to genes encoding heptosyltransferases. Each set of genes is variably present across NTHi strains and is located in a region of the genome with an alternative gene organization between strains that contributes to LPS heterogeneity. Dependent upon the strain background, the LPS phenotype, structure and serum resistance of strains mutated in these genes were altered when compared with the relevant parent strain. Our studies confirm that losB1 and losB2 usually encode DD-heptosyl- and LD-heptosyl transferases, respectively, and that losA1 and losA2 encode glycosyltransferases that play a role in OS extensions of NTHi LPS.
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| 6. |
- Fox, Kate L., et al.
(författare)
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Duplicate copies of lic1 direct the addition of multiple phosphocholine residues in the lipopolysaccharide of Haemophilus influenzae
- 2008
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Ingår i: Infection and Immunity. - 0019-9567 .- 1098-5522. ; 76:2, s. 588-600
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Tidskriftsartikel (refereegranskat)abstract
- The genes of the lic1 operon (lic1A to lic1D) are responsible for incorporation of phosphocholine (PCho) into the lipopolysaccharide (LPS) of Haemophilus influenzae. PCho plays a multifaceted role in the commensal and pathogenic lifestyles of a range of mucosal pathogens, including H. influenzae. Structural studies of the LPS of nontypeable H. influenzae (NTHI) have revealed that PCho can be linked to a hexose on any one of the oligosaccharide chain extensions from the conserved inner core triheptosyl backbone. In a collection of NTHI strains we found several strains in which there were two distinct but variant lic1D DNA sequences, genes predicted to encode the transferase responsible for directing the addition of PCho to LPS. The same isolates were also found to express concomitantly two PCho residues at distinct positions in their LPS. In one such NTHI isolate, isolate 1158, structural analysis of LPS from lic1 mutants confirmed that each of the two copies of lic1D directs the addition of PCho to a distinct location on the LPS. One position for PCho addition is a novel heptose, which is part of the oligosaccharide extension from the proximal heptose of the LPS inner core. Modification of the LPS by addition of two PCho residues resulted in increased binding of C-reactive protein and had consequential effects on the resistance of the organism to the killing effects of normal human serum compared to the effects of glycoforms containing one or no PCho. When bound, C-reactive protein leads to complement-mediated killing, indicating the potential biological significance of multiple PCho residues.
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