The amino-terminal domain of the P-pilus adhesin determines receptor specificity

Pyelonephritic isolates of Escherichia coli commonly express P-pili, which mediate bacterial attachment to glycolipids on epithelial cell surfaces. Three classes of P-pili have been defined, based on varying specificity for galabiose-containing glycolipids. Variation in adhesive capacity is correlated with a shift in preferred host, suggesting that host tropism depends largely on detailed specificity for the globoseries glycolipids. In this study we examined the importance of the PapG adhesin in determining receptor specificity. Translational fusions were constructed between the ammo-terminus of the PapG adhesin from each of the three pilus classes and a reporter protein. The binding specificity of the purified fusion proteins in vitro was identical to that seen with whole bacteria. Adherence of intact bacteria to cultured kidney cells was markedly reduced by a monoclonal antibody specific for the Class III adhesin (previously denoted PrsG), confirming the importance of the ammo-terminus of PapG in mediating attachment to a receptor when presented on the eukaryotic cell surface. These results suggest that the detailed receptor specificity resides solely within the amino-terminus of the PapG adhesin and is independent of the complex pilus architecture.     

Deoxyribonucleoside triphosphate metabolism and the mammalian cell cycle: Effects of thymidine on wild-type and dCMP deaminase-deficient mouse S49 T-lymphoma cells

The size of the dCTP pool has been implicated as a possible regulator of DNA synthesis. In this investigation we correlate large intracellular variations in deoxyribonucleoside triphosphate levels to the growth rates and cell-cycle kinetics of mouse S49 T-lymphoma cells. Wild-type and a mutant line AzidoC-100-5, lacking dCMP-deaminase activity resulting in a 10-fold expanded dCTP pool were studied and compared using flow cytometry, centrifugal elutriation and nucleoside triphosphate determinations. An increase in the dCTP pool was closely correlated to the passage of cells from G1 to S phase in both cell types. Addition of thymidine to wild-type and mutant cells resulted in an accumulation of cells in early S phase, concomitant with a decreased dCTP level. Mutant cells excreted large amounts of deoxycytidine into the medium which partially protected the cells from thymidine inhibition. The doubling times for the mutant and wild-type cells were very similar but the mutant had a somewhat prolonged S phase and shortened G1 phase compared with the wild-type cells. Large changes in the DNA precursor levels were produced by addition of thymidine to mutant cultures. This gave no change in the growth rate but a somewhat shortened S phase and prolonged G1. The biochemical background for these effects is discussed.     

Is the range size of migratory birds constrained by their migratory program?

Aim Intuitively, species in which the individuals migrate long distances between summer and winter quarters should be more likely to disperse and colonize new breeding areas than resident species. However, it has repeatedly been noted that many bird species with large ranges are residents. This paradox was tested on land birds breeding in the boreal forest of the Palaearctic, the largest uninterrupted stretch of habitat on earth. Methods The longitudinal distribution of two land bird communities on each side of the Eurasian continent, in Scandinavia and eastern Siberia, were used to test whether migratory birds indeed have a lower colonization success than resident birds. Results The migratory species are significantly less likely than resident species to have a range including both regions. The pattern held true even after controlling for latitudinal effects and local abundance, and was also observed at the level of genus and family. Main conclusions The relatively low colonization success of migratory species into new breeding areas may be because these new areas require novel migratory programs (migratory distance, direction and timing) in order for the birds to reach suitable wintering grounds.     

Photosystem I Is an Early Target of Photoinhibition in Barley Illuminated at Chilling Temperatures

Light-induced damage to photosystem I (PSI) was studied during low-light illumination of barley (Hordeum vulgare L.) at chilling temperatures. A 4-h illumination period induced a significant inactivation of PSI electron transport activity. Flash-induced P700 absorption decay measurements revealed progressive damage to (a) the iron-sulfur clusters F_A and F_B, (b) the iron-sulfur clusters F_A, F_B, and F_X, and (c) the phylloquinone A₁ and the chlorophyll A₀ or P700 of the PSI electron acceptor chain. Light-induced PSI damage was also evidenced by partial degradation of the PSI-A and PSI-B proteins and was correlated with the appearance of smaller proteins. Aggravated photodamage was observed upon illumination of barley leaves infiltrated with KCN, which inhibits Cu,Zn-superoxide dismutase and ascorbate peroxidase. This indicates that the photodamage of PSI in barley observed during low-light illumination at chilling temperatures arises because the defense against active oxygen species by active oxygen-scavenging enzymes is insufficient at these specific conditions. The data obtained demonstrate that photoinhibition of PSI at chilling temperatures is an important phenomenon in a cold-tolerant plant species.     

Experimental Lake Fertilization in the Kuokkel Area,Northern Sweden. Phytoplankton Biomass and Algal Composition in Natural and Fertilized Subarctic Lakes

Based on 500 quantitative algal analyses from 1971–1980 the seasonal variations of phytoplankton biomass and species diversity have been evaluated in one natural and three fertilized subarctic lakes. Enrichment with P alone did not cause any biomass increase and inhibited dinoflagellates and Dinobryon. Enrichment with N alone stimulated Uroglena and Gymnodinium and the biomass increased. No species were inhibited. Enrichment with both N and P made the biomass increase 50–60 times and the stimulated genera were: Chlorella, Choricystis, Chromulina, Chrysochromulina, Gymnodinium, Monoraphidium, Ochromonas, Spiniferomonas, Rhodomonas and Uroglena. In all fertilized lakes monocultures of chlorococcal green algae finally developed.