Hr. Statsgeolog

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Protective effect of bacterial lipopolysaccharides in the grapevine- Agrobacterium vitis interaction

Cell-associated lipopolysaccharides (LPS) were extracted by the phenol-chloroform-petroleum ether extraction method (PCP) from a nopaline strain of Agrobacterium vitis, purified by treatment with DNase/RNase, proteinase K and dialysis, characterized by polyacrylamide gel electrophoresis (SDS-PAGE), and bioassayed on grapevine shoot nodal segments. LPS preparation used for the experiments in planta was a mixture of rough-type LPS, obtained from precipitation with water after PCP-extraction, and some smooth- and rough-type LPS from the remaining phenol phase. Infiltration of an aqueous dispersion of the mixture in concentrations of 25-1000 µ g.ml-1 did not cause grapevine tissue necrosis, and callus formed within one month. When the LPS dispersions were infiltrated in the grapevine nodal segments, 24 h before challenge inoculation with A. vitis (5x102 cells per 5 µ l droplet), they prevented tumorgenesis and tissue necrosis; but, when the pathogen was inoculated at a higher concentration (5x105 cells per 5 CII droplet), these LS applications were active in protecting plant tissue from necrosis and did not prevent tumor induction. The potential role of LPS as candidate molecules in the protection of grapevine from A. vitis infection is discussed

Truncated glucagon-like peptide I, an insulin-releasing hormone from the distal gut

AbstractBy hydrophobic gel permeation and high pressure liquid chromatography we isolated from pig intestinal mucosa a peptide which corresponds to proglucagon 78–107 as suggested by chromatography and determination of its N-terminal sequence. Natural and synthetic proglucagon 78–107 dose dependently and potently increased insulin secretion from the isolated perfused pig pancreas. Proglucagon 78–107 also secreted by the small intestine may participate in the hormonal control of insulin secretion

Tp53 mutation is a prognostic factor in lower grade glioma and may influence chemotherapy efficacy

Background: Identification of prognostic biomarkers in cancers is a crucial step to improve overall survival (OS). Although mutations in tumour protein 53 (TP53) is prevalent in astrocytoma, the prognostic effects of TP53 mutation are unclear. Methods: In this retrospective study, we sequenced TP53 exons 1 to 10 in a cohort of 102 lower-grade glioma (LGG) subtypes and determined the prognostic effects of TP53 mutation in astrocytoma and oligodendroglioma. Publicly available datasets were analysed to confirm the findings. Results: In astrocytoma, mutations in TP53 codon 273 were associated with a significantly increased OS compared to the TP53 wild-type (HR (95% CI): 0.169 (0.036–0.766), p = 0.021). Public datasets confirmed these findings. TP53 codon 273 mutant astrocytomas were significantly more chemosensitive than TP53 wild-type astrocytomas (HR (95% CI): 0.344 (0.13–0.88), p = 0.0148). Post-chemotherapy, a significant correlation between TP53 and YAP1 mRNA was found (p = 0.01). In O (6)-methylguanine methyltransferase (MGMT) unmethylated chemotherapy-treated astrocytoma, both TP53 codon 273 and YAP1 mRNA were significant prognostic markers. In oligodendroglioma, TP53 mutations were associated with significantly decreased OS. Conclusions: Based on these findings, we propose that certain TP53 mutant astrocytomas are chemosensitive through the involvement of YAP1, and we outline a potential mech-anism. Thus, TP53 mutations may be key drivers of astrocytoma therapeutic efficacy and influence survival outcomes

Regional Impact of Retiring Whole Farms

Suppose the government adopted a program of returing marginal land on a whole farm basis. What would happen to the Corn Belt in 1965 if the major goal were to balance supply demand? Where would the nation stand in 1975

Identification and structural determination of the capsular polysaccharides from two Acinetobacter baumannii clinical isolates, MG1 and SMAL

The structures of the capsular polysaccharides (CPSs) of the two clinical isolates Acinetobacter baumannii SMAL and MG1 were elucidated. Hot phenol/water extractions of the dry biomasses, followed by enzymatic digestions and repeated ultracentrifugations led to the isolation of polysaccharides that were negative in Western blot analysis utilizing an anti-lipid A antibody, thus proving that they were not the LPS O-antigens but CPSs. Their structures were established on the basis of NMR spectroscopy and GC-MS analyses. The A. baumannii MG1 CPS consisted of a linear aminopolysaccharide with acyl substitution heterogeneity at the N-4 amino group of QuipN4N: 4)-alpha-D-GlcpNAc-(1 -> 4)-alpha-L-GalpNAcA-(1 -> 3)-beta-D-QuipNAc4NR-(1 -> R = -3-hydroxybutyrryl or acetyl. The repeating unit of the CPS produced by strain SMAL is a pentasaccharide, already reported for the O-antigen moiety from A. baumannii strain ATCC 17961: beta-D-GlcpNAc3NAcA-(1 down arrow 4) 6)-beta-D-Glcp-(1 -> 3)-beta-D-GalpNAc-(1 -> 3)-alpha-D-Galp-(1 -> 6)up arrow beta-D-GlcpNAc-(

Enriching Thermal Point Clouds of Buildings using Semantic 3D building Models

Thermal point clouds integrate thermal radiation and laser point clouds effectively. However, the semantic information for the interpretation of building thermal point clouds can hardly be precisely inferred. Transferring the semantics encapsulated in 3D building models at Level of Detail (LoD)3 has a potential to fill this gap. In this work, we propose a workflow enriching thermal point clouds with the geo-position and semantics of LoD3 building models, which utilizes features of both modalities: model point clouds are generated from LoD3 models, and thermal point clouds are co-registered by coarse-to-fine registration. The proposed method can automatically co-register the point clouds from different sources and enrich the thermal point cloud in facade-detailed semantics. The enriched thermal point cloud supports thermal analysis and can facilitate the development of currently scarce deep learning models operating directly on thermal point clouds