Inhibition of RNA Polymerase by Streptolydigin

TWO antibiotics inhibit RNA synthesis by interacting directly with RNA polymerase. The rifamycin series^1–3 inhibit before RNA chain initiation and are without apparent effect during polymerization. Streptolydigin, however, inhibits initiation and chain elongation^4–9. Using the d(A-T)-directed reaction as a model system¹⁰, we will show that streptolydigin stabilizes the polymerase-template interaction.     

Nest-site philopatry and selection for environmental sex determination

The reason for the frequent occurrence of environmental sex determination (ESD) in reptiles is still not well understood, although much effort has been devoted to solving the issue. Stimulated by the occurrence of nest-site philopatry in some species, this paper examines a diploid model of the influence of nest-site philopatry on the evolution of ESD. Analysis shows that nest-site philopatry can lead to ESD because the fitnesses of sons and daughters are not influenced in the same way by nest-site quality. Daughters inherit the nest site and thus benefit more than sons from a high-quality nest site. Conversely, the fitness of daughters at low-quality nest sites is lower compared to the fitness of sons. Therefore, genes causing ESD can spread by causing the production of more sons at low-quality nest sites and more daughters at high-quality nest sites. Suggestions are made to test empirically whether nest-site philopatry led to the evolution of ESD. This revised version was published online in July 2006 with corrections to the Cover Date.     

Inheritance of Autogamy and the Killer Trait in Euplotes minuta

SYNOPSIS. Eight interfertile strains of Euplotes minuta collected from two localities in the Mediterranean Sea are shown to comprise a single breeding system of multiple mating types. One strain regularly passes through autogamy and, in crosses to non-autogamous strains, preliminary evidence for the genic control of autogamy was obtained. The cytogenetic events of conjugation and autogamy are briefly described. Three strains are "killers." Killer cells liberate a substance into the surrounding medium which has a lethal effect on cells of other strains called "sensitives." This substance, "euplotein," is not produced by sensitives. The inheritance of the killer trait is apparently under the control of a cytoplasmic factor but present attempts to identify the factor microscopically were without success. The discussion stresses the potential usefulness of this species for studies of protozoan genetics and development.     

The Effect of N-nutrients on the Acceptor Pool of PS I and Thylakoid Energization as Measured by Chlorophyll Fluorescence of Dunaliella salina

Changes of PS II chlorophyll fluorescence of Dunaliella salinawere used to study the effect of micromolar concentrations ofN-nutrients (nitrate, nitrite and ammonia) on photosyntheticelectron flow. The responses were evoked by changes in lightintensity which were controlled by a special protocol. Thisenabled the splitting of the overall response into individualcomponents by curve fitting and the assignment of these componentsto particular reactions of the photosynthetic apparatus. Byvirtue of a comparison with simultaneously measured changesin transmission at 532 ran, the identification could be madeof the component which is related to redox changes of the acceptorpool of PS I. The time-constant related to this acceptor pool was found toincrease by a factor of up to 5 after the addition of N-nutrients.The results indicate that the addition of N-nutrients increasesthe acceptor pool of PS I. The relationship between nutrientconcentration and effect is not consistent. In contrast to theelectron flow to the Calvin cycle, the electron flow to nitrogenassimilation is not related to a strong consumption of ATP.Thus, it gives rise to an increase in the transthylakoid pHgradient. The expected increase in the kinetic component ofchlorophyll fluorescence related to thylakoid energization isobserved after the addition of nitrate. Key words: Chlorophyll fluorescence, noise, N-nutrient metabolism, time-constants, thylakoid energization     

Comparative size,biomass, elemental composition (C,N, H), and energy concentration of caridean shrimp eggs

Summary

In the evolution of decapod crustaceans, interspecific variation in egg size is considered as an important life-history trait that is linked with the duration of embryonic and larval development, the number and type of larval stages, and with juvenile size. Aiming to provide a quantitative characterization of reproductive traits in related decapod taxa differing in lifestyle (freshwater, estuarine, marine) and geographic-climatic distribution (tropical-temperate), we compared size, biomass, and elemental composition of eggs of caridean shrimps from three families: seven species of Palaemonidae (three congeners of Macrobrachium: M. olfersii, M. carcinus, M. acanthurus; four species of Palaemon: P. northropi, P. pandaliformis, P. elegans, P. adspersus), two Atyidae (Potimirim potimirim, Atya scabra), and one Pandalid (Pandalus montagui). Egg size was measured as larger and smaller diameter (D₁ D₂), volume was calculated from D₁ and D₂, and biomass was measured as dry mass (W), carbon (C), nitrogen (N), hydrogen (H), and energy (E, estimated from C) contents. The smallest size and lowest biomass were found in the eggs of two freshwater atyids (both originating from Brazil); the largest size occurred in a marine species, P. montagui (from the North Sea); and intermediate values in freshwater, estuarine, and marine palaemonid species (from Brazil and the Baltic Sea, respectively). Among the Palaemon species, the most limnic (P. pandaliformis) showed a significantly larger egg size and volume (P<0.001) than the estuarine and marine congeners, P. elegans, P. adspersus and P. northropi. This suggests that the generally postulated relationship between egg size and lifestyle (freshwater vs. estuarine or marine) may appear at a generic but not at the family level. On the other hand, individual biomass (in μg or Joules per egg) of early eggs was significantly higher in P. elegans and P. adspersus, indicating interspecific variability in biomass and energy concentration (in μg or Joules per unit volume, mm³). Generally lower biomass concentrations in early eggs of freshwater shrimps may be caused by a higher average water content. Eggs in late embryonic stages were generally larger than earlier eggs of the same species, reflecting an increase in the water content, while an increasing D₁:D₂ quotient indicated an increasingly elongated egg shape. The biomass per egg decreased during embryonic development due to metabolic degradation of organic reserves. As a consequence of inverse ontogenetic changes in size and organic biomass of developing eggs, the mass-specific biomass values (C, N, H in percent of W; E in Joules per mg W) and volume-specific concentrations (μg or Joules per unit volume) decreased. This change was consistently stronger in the C, H, and E contents than in other measures of biomass (W, N). In consequence, the C:N mass ratio also decreased, suggesting that lipid degradation rather than protein utilization was the principal fuel for embryonic development. Our results indicate high intra- (mainly developmental) and interspecific variation in reproductive traits of closely related species. While volume-specific biomass and energy concentrations of early eggs appear to be associated with variation in habitat salinity (freshwater, brackish, marine), individual egg size and biomass may be related more with the climatic-geographic distribution (temperate, tropical) of different taxa.     

Inhibition of Pair Formation by Concanavalin A and Concanavalin A-Binding Glycoconjugates in Euplotes octocarinatus

ABSTRACT. Concanavalin A (≥ 50 μg/ml) inhibits pair formation in both of the two complementary mating types of Euplotes octocarinatus studied in this investigation. This effect can be reversed by methyl-α- d -mannose. Concanavalin A is accessible for methyl-α- d -mannose until pairs are formed. Methyl-α- d -mannose as well as methyl-α- d -glucose and 2-acetamido-2-deoxy- d -glucose alone do not inhibit pair formation unless applied in concentrations ≥ 60 mM. The Concanavalin A-sensitive phase of preconjugant interaction starts 2 h after cells are induced to conjugate. Based on these observations we suggest that Concanavalin A might exhibit its action by binding to carbohydrate moieties of preconjugation-specific adhesion molecules and thereby might allosterically block interactions with their counterparts. To identify preconjugation-specific alterations in number or localization of Concanavalin A-binding glycoconjugates, we probed western blots of total cell proteins or fixed cells, respectively, with digoxigenin-labeled Concanavalin A. On Concanavalin A blots 20 different Concanavalin A-binding glycoconjugates were identified in mating-competent cells. Localization of Concanavalin A-binding sites on mating-competent cells by light microscopy resulted in predominant labeling of a comma-shaped structure near the paroral membranelle. During the preconjugation period no changes in number or localization of Con A-binding glycoconjugates were detected. Possible reasons are discussed.