La dormance embryonnaire chez Taxus baccata: Influence de la composition du milieu liquide sur I'induction de la germination Par

Embryo dormancy of Taxus baccata var. fastigiata is eliminated when cultured continuously in nutritive liquid medium. An equivalent percentage of germination is obtained when the embryos are transferred to agar medium after 8 days of liquid culture. There is no morphological development of the embryo during the period in the liquid medium. But we have ascertained that water-soluble germination inhibitors present in the embryo are leached out into the medium, permitting germination. Germination is totally absent when the embryos are cultured continuously in distilled water, alone or with minerals; incidental in sucrose solution; and maximal when the medium contains sucrose and Ca²⁺ or K⁺ ions. The extent of germination on agar medium depends upon the composition of the liquid medium in which the embryos are cultured for the initial 8 days. But this preliminary culture in the liquid medium does not always remove the endogenous inhibitors, irrespective of its composition. This can be achieved only in the presence of sucrose; and this process can be made more effective by the addition of Ca²⁺ ions.     

Facilitated Penetration of Amanitin—Albumin Conjugates into Hepatocytes after Coupling with Fluorescein

α-AMANITIN, a cyclic peptide of the toadstool Amanita phalloides^1,2, causes necrosis of liver and kidney cells, the first morphological lesions occurring in the nuclei^3,4. It acts by binding to RNA polymerase in eukaryotic .cells and inhibiting the enzyme^5–9. The hepatotoxicity of amanitin increases several times when it is conjugated to albumin, probably because of a slower rate of elimination of the toxin through the glomeruli^4,10. It is unlikely that the amanitin-albumin conjugate enters the hepatocyte by a mechanism involving its albumin moiety; it was therefore suggested¹¹ that penetration of the liver cells is consequent on binding of the amanitin group to the carrier involved in transport of this peptide. This led us to consider more generally the facilitation of penetration into cells by large molecules by means of binding to another molecule for which a carrier exists on the cell membrane^12,13.     

Differential regulation of rat insulin I and II messenger RNA synthesis: effects of fasting and cyproheptadine

Rats and mice retain a duplicated insulin (I) gene. Because the duplicated gene shares only incomplete homology with the ancestral insulin (II) gene it may be regulated differently. In the studies presented here we measured changes in abundance of these distinct insulin mRNAs and their precursors in response to fasting and fasting plus a single dose of cyproheptadine, two experimental manipulations that cause changes in the level of total insulin mRNA in rats. Both diminished rat insulin II mRNA to a greater extent than rat insulin I mRNA. Rat insulin II mRNA comprised 41% of the total insulin mRNA in 0 h controls and decreased to 33% of the total insulin mRNA after a 10-h fast. Insulin II mRNA decreased to 26% of the total insulin mRNA 10 h after treatment with cyproheptadine. To determine whether these manipulations had effects on insulin mRNA synthesis, precursors for each of the two mRNAs were quantified. Fasting for 24 h had only small effects on insulin I mRNA precursor, but diminished rat insulin II pre-mRNA to 32% of the 0 h control values. One and a half hours after fasting plus cyproheptadine administration, pre-mRNA for rat insulin II levels had decreased to 38%, while rat insulin I pre-mRNA remained at levels present in 0 h controls. Levels of rat insulin I and II pre-mRNAs were both maximally depressed at 10 h, but rat insulin II pre-mRNA decreased to 3%, while rat insulin I pre-mRNA diminished to only 49% of controls.(ABSTRACT TRUNCATED AT 250 WORDS)     

Facies-dependent δ13C variation from a Cryogenian platform margin,South Australia: Evidence for stratified Neoproterozoic oceans?

Analysis of a Cryogenian interglacial platform margin in the Adelaide Geosyncline reveals a strong carbonate δ¹³C-facies relationship. Detailed chronostratigraphic correlation between sections ranging from shallow platform facies to deep basinal facies indicates the presence of a carbon isotopic gradient of between 8 and 11‰ in time-equivalent strata. Shallow-water back-reef facies have δ¹³C values up to 8.2‰, while equivalent basinal sediments have δ¹³C values between ? 3 and 0‰. Allochthonous blocks that have been transported from the platform margin into basinal environments retain their heavy δ¹³C values (4–9‰) and are surrounded by basinal calcareous shales with light δ¹³C values (ave. 0.8‰). The regional and stratigraphic consistency of these δ¹³C trends suggests a primary marine origin.We interpret this δ¹³C-facies correlation to be the result of ocean stratification/stagnation that significantly reduced the rate of deep-ocean ventilation and produced a large deep-water, organically derived carbon reservoir. We suggest that stratification may have been a persistent feature of the global ocean throughout much of Neoproterozoic time. Ocean stratification may explain many of the unusual features that characterise the sedimentary record of this era, including large-scale δ¹³C variation, extreme climatic fluctuations, and the presence of cap carbonates. A highly variable climatic regime would be expected with the development of a large deep-water carbon reservoir. Small changes in ocean circulation could rapidly transfer or remove large volumes of carbon to and from the surface-ocean and atmospheric reservoirs, leading to intense greenhouse or icehouse conditions respectively.     

Conversion of Phosphatidyl Choline to Phosphatidic Acid in Freeze Injured Rye and Wheat Cultivars

The effect of exposure to freezing temperature (?15°C) on leaf phospholipid composition of hardened rye (Secale cereale L.) and hardened wheat cultivars (‘Miranovskaja 808’, ‘Bezostaja 1’, ‘Short Mexican’ and ‘Penjamo 62’), which differ in their resistance to frost, was investigated. Hardening took place under natural conditions. All the seedlings attained an equal level of linolenic acid in their leaves during hardening. Exposure to freezing temperatures resulted in a loss of phosphatidyl choline and accumulation of phosphatidic acid in the leaves. The ratio of phosphatidic acid to phosphatidyl choline, but not the level of poly-unsaturated fatty acids in the leaves, was related to their ability to survive at low temperatures. As freezing injury is caused by the formation of ice crystals in both extra- and intracellular space, it is probable that the plasma membranes of the investigated cultivars differed with respect to their water permeability. It is concluded that the plants, depending on the degree of their resistance to cold, produce an unknown substance of lipidic nature upon exposure to cold, with the aid of which they adjust the transitional state of their membranes to the prevailing temperature and, at the same time, facilitate the efflux of water from the cells.