Cooperative Use of VCD and XRD for the Determination of Tetrahydrobenzoisoquinolines Absolute Configuration: A Reliable Proof of Memory of Chirality and Retention of Configuration in Enediyne Rearrangements

The absolute configurations (AC) of azaheterocylic compounds resulting from the cascade rearrangement of enediynes involving only light atoms were unambiguously assigned by the joint use of vibrational circular dichroism (VCD) and copper radiation single crystal X‐ray diffraction (XRD). These AC determinations proved that the rearrangements of enediynes proceeded with memory of chirality and retention of configuration. Chirality 25:832–839, 2013. © 2013 Wiley Periodicals, Inc.     

Respiratory components in acidophilic bacteria that respire on iron

Abstract

Microorganisms capable of aerobic respiration on ferrous ions are spread throughout eubacterial and archaebacterial phyla. Phylogenetically distinct organisms were shown to express spectrally distinct redox‐active biomolecules during autotrophic growth on soluble iron. A new iron‐oxidizing eubacterium, designated as strain Funis, was investigated. Strain Funis was judged to be different from other known iron‐oxidizing bacteria on the bases of comparative lipid analyses, 16S rRNA sequence analyses, and cytochrome composition studies. When grown autotrophically on ferrous ions, Funis produced conspicuous levels of a novel acid‐stable, acid‐soluble yellow cytochrome with a distinctive absorbance peak at 579 nm in the reduced state.

Stopped‐flow spectrophotometric kinetic studies were conducted on respiratory chain components isolated from cell‐free extracts of Thiobacillus ferrooxidans. Experimental results were consistent with a model where the primary oxidant of ferrous ions is a highly aggregated c‐type cytochrome that then reduces the periplasmic rusticyanin. The Fe(II)‐dependent, cytochrome c‐catalyzed reduction of the rusticyanin possessed three kinetic properties in common with corresponding intact cells that respire on iron: the same anion specificity, a similar dependence of the rate on the concentration of ferrous ions, and similar rates at saturating concentrations of ferrous ions     

Fluorometric, Chromatographic, and Spectronic Evidence for the Non-indolic Nature of Citrus Auxin

Evidence for the non-indolic nature of the new citrus auxinis presented on the basis of fluorometric properties, thin-layerchromatography, Ehrlich's colour reaction, paper electrophoresis,and the infra-red spectra determinations. Citrus auxin had alower Rf in TLC than IAA, did not give the typical indole reactionwith Ehrlich's reagent, and behaved differently in electrophoresis.The infra-red spectra also provided preliminary informationconcerning chemical structure. The hypothesis that indolic compoundsconstitute the only natural auxins in higher plants should berevised in view of this evidence that a non-indole auxin existsin higher plants.     

Thermopreferendum de l'Araignée socialeAgelena consociata Denis

Résumé Le présent article a pour but d'analyser les multiples facteurs pouvant perturber l'étude duthermopreferendum de l'Araignée socialeAgelena consociata Denis et d'exposer les résultats obtenus.Pour satisfaire lethigmotactisme très développé de ces Araignées, la boîte servant à cette étude est cloisonnée et sa hauteur est de 1 cm.Un abreuvoir placé dans chaque compartiment maintient une humidité saturante pour compenser le gradient hygrométrique résultant du gradient thermique.L'expérience doit durer plusieurs jours et ne commencer que 24 heures après l'introduction des Araignées: premièrement, parce que cela permet aux Araignées de recouvrir le fond de la boîte d'une nappe de soie, ce qui contribue à les rapprocher de leurs conditions naturelles; deuxièmement, parce que la phase d'activité de ces Araignées est nocturne. Or, il semble que c'est lors de cette phase que les animaux choisissent leurthermopreferendum.Il ne faut pas effectuer plus de trois relevés par jour, sans quoi les Araignées, très sensibles aux perturbations, ont tendance à se diriger vers l'extrémité froide.Lethermopreferendum desAgelena consociata se situe à 22°65±0,10 pour la température de l'air et à 22°89±0,12 par rapport à la température du sol.

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Summary This article aims at analysing the various causes which can disturb the study of thethermopreferendum of social SpidersAgelena consociata Denis and aims at explaining the achieved results.In order to satisfy the extremely developedthigmotactisme of these Spiders, the box used for that study has been partitioned off; its height is 1 cm.A small piece of wet cotton-wool placed into each partition maintains a saturated humidity to compensate the hygrometric gradient resulting from the thermic gradient.The experiment must go on during several days and must only begin a day after having put the Spiders into the box: first because the Spiders can cover the bottom with a cobweb, which contributes to create almost natural conditions; secondly because the period of activity of these Spiders takes place at night. As a fact it seems that it is during this period that the Spiders choose theirthermopreferendum.More than three readings a day must not be performed because otherwise the Spiders, wich are very sensitive to disturbances, are inclined to go towards the cold end of the box.Thethermopreferendum of theAgelena consociata takes place at 22°65 C±0,10 C as for the temperature of the air and at 22°89 C±0,12 C as for the temperature of the ground.

     

Azure a-Schiff, Alcian Blue, HIO4-Schiff, Naphthol Yellow S—A Sequential Staining Method for Paraffin Sections

Paraffin sections from tissue fixed 4-12 hr in 10% formalin containing 0.5% cetyl pyridinium chloride, and washed 2 hr, were stained as follows: (1) Hydrolyze in 5 N HCl at room temperature for 8.5-9 min, or use standard Feulgen hydrolysis at 60 C. (2) Stain in azure A-Schiff, 0.5% in bisulfite bleach (1 N HCl, 5; 10% Na₂S₂O₅, 5; and distilled water 90—parts by volume) for 10 min. (3) Place in bisulfite bleach 2 changes, 2 min each; wash in water, 1-2 min. (4) Stain in Alcian blue (0.1% in 0.01 2V HCl, pH 2.0) for 10 min. (5) Place in 0.01 N HCl for 2-3 min; wash in water for 1-2 min. (6) Oxidize in 0.5% HIO₄ for 5 min; wash in water, 1-2 min. (7) Stain in Schiff's leucofuchsiu, 10 min. (8) Treat with bisulfite bleach as in step 3; wash in running water, 10 min. (9) Stain in naphthol yellow S (0.01% in 1% acetic acid) for 1-2 min. (10) Place in 1% acetic acid for 2 min, dehydrate in tertiary butanol, clear and cover. Result: DNA is deep blue; acidic mucins are light blue; neutral polysaccharides, red to magenta; and proteins, yellow. Proper timing of the hydrolysis for the Feulgen reaction is the most critical step. Overhydrolysis results in green nuclei (staining by naphthol yellow S) whereas purplish nuclei are the results of insufficient hydrolysis.     

Fibrinogen and platelet aggregation. Role of the glycopeptidic part and of the fibrinopeptide B: Description of a new technique of fibrinoglycopeptide isolation

In order to determine the active groups of the fibrinogen molecule in ADP induced aggregation, various cleavage fragments of fibrinogen were tested on plasma protein-free platelets. An original technique is described for the isolation of fibrinogen glycopeptides. The glycopeptides thus obtained exert an inhibition on platelet aggregation by ADP in the presence of fibrinogen, when incubated previously with the plasma protein free platelets. The carbohydrate fraction seems thus to have an important role on ADP platelet aggregation.The N. DSK and E fragments are inactive as cofactors of ADP induced aggregation.It is suggested that the N-terminal part of the Bβ chain does not have an important role in the cofactor activity of fibrinogen. Moreover, the importance of an intact fibrinogen molecule is underlined.