Nordic equiseticolous Pyrenomycetes

The Pyrenomycete flora on Equisetum has been studied, mainly on Nordic material. With regard to frequency and host specificity these fungi can be divided into three groups, viz. 1) true Equisetum fungi; 2) common species but not restricted to Equisetum; 3) accidental species. An annotated list is given of the two first categories which comprise the following taxa. 1: Didymosphaeria equiseti–hiemalis, Phaeosphaeria berlesei, P. equiseti, Mycosphaerella equiseti, M. equiseticola, Scirrhia castagnei, S. silvalica , and probably Didymella equisetina. 2: Phaeosphaeria eustoma, P. fuckelii, Mycosphaerella cf. aspidii.
Two new taxa and one new combination are published, viz. Phaeosphaeria equiseti (Karst.) L. & K. Holm comb, nov., P. equiseti var. lindii L. & K. Holm var. nov., Scirrhia silvalica L. & K. Holm sp. nov.     

Social interactions among breeding Brünnich's Guillemots Uria lomvia suggest constraints in relation to offspring vulnerability

Brünnich's Guillemots Uria lomvia are adapted to high-density breeding in large colonies on steep cliffs. Because they breed on narrow ledges, egg loss through dislodgement is an important cause of breeding failure. Fighting among breeders presumably raises the risk of accidental dislodgement. In this study, we investigated whether social behaviour among Brünnich's Guillemots shows any adaptations to reduce accidental egg loss by modifying behaviour during incubation. We found that the amount of aggression increased significantly at the time of hatching, perhaps in response to the reduced risk of breeding failure through dislodgement of a chick, compared with an egg. Allopreening followed an inverse trend, falling significantly after the day of hatch. This supports the hypothesis that allopreening is used to reduce aggressive interactions. At the same time, the frequency of allopreening was greatly increased on days when mosquitoes affected the birds, consistent with the hypothesis that allopreening is part of a defence strategy against ectoparasites.     

Biosorption of copper by yeasts

Summary The ability to accumulate copper from aqueous solutions was determined with different yeast species. Yeast cells did not show any significant differences in process kinetics. The uptake was very fast and was influenced by environmental factors. The metal-accumulating capacity differed among the tested strains. The yeastsCandida tropicalis andPichia guilliermondii were chosen for extensive research. Cells of the stationary growth phase were able to adsorb a high amount of copper. The uptake capacity decreased with increasing biomass concentration. Copper adsorption obeyed the Freundlich isotherm. Optimal pH range was between 5 and 7. The biomass could be used repeatedly for biosorption after desorption by mineral acids.     

Kinetics of lymphocyte stimulation in vitro by non-specific mitogens

The role of mitogens during lymphocyte activation was studied with kidney bean leucoagglutinin, concanavalin A and kidney bean phytohemagglutinin. The mitogens were removed by treatment with appropriate antisera, which was demonstrated to remove also mitogens already attached to the cells. The process of lymphocyte activation in vitro can be divided into four distinct steps, three of which are mitogen-dependent and the fourth is mitogen-independent. The first step consists of attachment of the stimulatory molecules to the cell membrane. The second step consists of reaction between mitogen and an activating system. During these two phases the cells become preactivated. The establishment of a preactivated state involves at least some synthesis of cytoplasmic RNA. The preactivated state is reversible and during the third step of lymphocyte activation the final result of preactivation is determined. Depending on the presence or absence of mitogen the cells may remain preactivated for over 60 h, they may return to the resting state or they may proceed through the final stages of the proliferation cycle and eventually divide. This fourth step is independent of the presence or absence of mitogen. A prolonged contact between cells and mitogen is required during the mitogen-dependent steps. The process of lymphocyte activation by mitogen is thus continuously being regulated by the stimulatory molecules on the lymphocyte membrane, which may be of considerable significance also for in vivo immunologicai reactions at the cellular level.     

Calcium dependency of the binding and mitogenicity of phytohemagglutinin: Differentiation between calcium-dependent and independent binding events

The same amount of phytohemagglutinin binds to lymphocytes at 37 °C and at 0 °C. The binding is inhibited by calcium chelators at 37 °C, but not at 0 °C, during the very first minutes of contact between lectin and cells. N-Acetylgalactosamine in high concentrations inhibits binding at both temperatures. The binding at 0 °C is abortive in the sense that it does not result in subsequent DNA synthesis. These findings indicate that the binding of phytohemagglutin (PHA) to the glycoprotein receptor on the cell surface does not in itself activate the immediate transducer of the mitogenic signal. The binding has to be accompanied by some change which involves calcium and occurs very rapidly, but cannot take place at 0 °C, to give a proper mitogenic anchorage of PHA to the cells.     

On the mechanism of action of 15-methyl-PGF2α as an abortifacient

Several hours following administration of long acting vaginal suppositories containing 3.0 mg of 15-methyl-PGF_2α for interruption of second trimester pregnancies there is an up to 10-fold increase in endogenous production of PGE₂ and PGF_2α before abortion as reflected by gas chromatographic-mass spectrometric determination of the major plasma metabolites of PGE₂ and PGF_2α. The data suggest that this increased formation of endogenous prostaglandins contributes to the induced uterine activity during the latter part of the abortion process.     

Identification of Akt pathway inhibitors using redistribution screening on the FLIPR and the IN Cell 3000 analyzer

The PI3-kinase/Akt pathway is an important cell survival pathway that is deregulated in the majority of human cancers. Despite the apparent druggability of several kinases in the pathway, no specific catalytic inhibitors have been reported in the literature. The authors describe the development of a fluorometric imaging plate reader (FLIPR)-based Akt1 translocation assay to discover inhibitors of Akt1 activation. Screening of a diverse chemical library of 45,000 compounds resulted in identification of several classes of Akt1 translocation inhibitors. Using a combination of classical in vitro assays and translocation assays directed at different steps of the Akt pathway, the mechanisms of action of 2 selected chemical classes were further defined. Protein translocation assays emerge as powerful tools for hit identification and characterization.     

Evidence for an RNA chaperone function of polypyrimidine tract-binding protein in picornavirus translation

The cellular polypyrimidine tract-binding protein (PTB) is recruited by the genomic RNAs of picornaviruses to stimulate translation initiation at their internal ribosome entry site (IRES) elements. We investigated the contribution of the individual RNA recognition motif (RRM) domains of PTB to its interaction with the IRES of foot-and-mouth disease virus (FMDV). Using a native gel system, we found that PTB is a monomer, confirming recent reports that challenged the previous view that PTB is a dimer. Mapping the spatial orientation of PTB relative to the bound IRES RNA, we found that the two C-terminal RRM domains III and IV of PTB bind in an oriented way to the IRES. Domain III contacts the IRES stem-loop 2, while domain IV contacts the separate IRES 3' region. PTB domain I appears not to be involved directly in RNA binding, but domain II stabilizes the RNA binding conferred by domains III and IV. A PTB protein containing only these two C-terminal PTB domains is sufficient to enhance the entry of initiation factor eIF4G to the IRES and stimulate IRES activity, and the long-lived PTB-IRES interaction stabilized by domain II is not a prerequisite for this function. Thus, PTB most likely acts as an RNA chaperone to stabilize IRES structure and, in that way, augment IRES activity.