Use of Edman's method for splitting actinoidin peptides and aglycone

Phenylthiohydantoins of amino acids isolated from actinoidine (n-oxyphenylglycine, 3-chlor-4-oxyphenylglycine, actinoidinic amino acid) were prepared. Their spectral and chromagraphic properties were studied. Splitting of the aglycone of actinoidine and the prodlcts of its incomplete acid hydrolysis (peptides Y-Phe and B-Y-Phe) was achieved with the Edman method. Parital structure of tripeptide B-Y-Phe (4NH2-group) was proposed. Tripeptide B-Y Phe constitutes about 80 per cent of the antibiotic aglycone part.     

Prioritisation of abstraction boreholes at risk from chlorinated solvent contamination on the UK Permo-Triassic Sandstone aquifer using a GIS

A 250 km2 area of the Permo-Triassic Sandstone aquifer in the West Midlands of England, UK, was selected as a test region for the development of a geographic information system (GIS)-based risk assessment methodology that incorporates contaminant source, groundwater vulnerability and groundwater abstraction catchment elements in order to prioritise areas and boreholes potentially at risk from chlorinated solvent pollution on a regional scale. Factors incorporated in the vulnerability assessment include the nature of soils, presence or absence of superficial or glacial deposits, fault density and depth to water table. ARCVIEW GIS was employed with a simple ranking system from which the derived vulnerability assessment index was combined with current chlorinated solvent user industry data and source protection zone components. Results indicate the presence of high-risk areas in urban locations where locally dense distributions of chlorinated solvent user industries combine with high vulnerability aquifers within the catchment of supply boreholes. Ranking of catchment-specific risk reveals the abstraction points under greatest stress. The proposed methodology has applications as a regional-scale initial screening tool to guide site selection for regulatory inspections and assist in prioritising monitoring strategies for existing boreholes. Future developments will provide guidance for locating new urban boreholes in areas of lowest risk.     

Suppression of breast xenograft growth and progression in nude mice: implications for the use of orally administered sphingolipids as chemopreventive agents against breast cancer

Sphingolipids are lipid messengers involved in the regulation of many different cellular processes. Sphingolipid enzymes and bioactive metabolites have been targets of in vitro and in vivo efforts to suppress cancer growth, progression and metastasis of various cancer types. Dietary sphingomyelin effectively suppressed colon cancer in several rodent models without causing toxic side effects. In the present study, we determined if the effect of sphingolipid metabolites derived from the hydrolysis of dietary sphingomyelin is restricted to the intestinal tract or if their systemic concentrations are sufficient to suppress cancers of distant sites. For these studies, we used MCF10AT1 cells, a model for progressive breast cancer, injected into the mammary fatpad of nude mice as a single cell suspension. The mice were fed 0.1% sphingomyelin supplements in a semi-purified AIN76A control diet when the lesions were palpable. The study was terminated when the first lesions had grown to 5 mm. In the sphingomyelin-fed group, there was a trend to smaller lesion size and, importantly, a delayed progression to more malignant stages without apparent side effects. This may be the result of significantly reduced rates of proliferation and angiogenesis, while no increase of apoptosis was detected. Changes in aberrantly expressed proteins in the sphingomyelin-fed group, such as E-cadherin, VEGF and sphingosine kinase-1, may be associated with the suppression of tumor growth. These results demonstrate that diet-derived sphingolipids can efficiently suppress the growth and progression of MCF10AT1 xenografts, suggesting that dietary sphingomyelin may also be effective against cancers of other sites.