Etude de la composition en sucres de souches de Conidiobolus saprophytes ou pathogenes pour l'homme et l'animal

Résumé La composition en sucres des parois de 13 souches de Conidiobolus coronatus et de 1 souche de Conidiobolus incongruus a été étudiée par chromatographie en phase gazeuse. Deux sucres principaux ont été mis en évidence: du glucose et du mannose. L'étude du rapport mannose/ glucose montre que les souches se répartissent en 3 groupes. Dans le premier groupe figurent les souches de C. coronatus ayant un rapport compris entre 0,92 et 1,3; ces souches ont été isolées de l'homme et du chimpanzé. Dans le second groupe figurent les souches de C. coronatus isolées du sol ou des lésions du cheval dont le rapport varie de 2,7 à 4,1; enfin, à part, Conidiobolus incongruus qui est caractérisé par un rapport de 0,44. La température léthale de chacune des souches étudiées ainsi que la présence éventuelle de spores villeuses est également signalée. Deux séries apparaissent donc chez Conidiobolus coronatus qui correspondent peut-être à des groupes biologiques différents.

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The composition in the cell wall sugars of 13 strains of Conidiobolus coronatus and 1 strain of Conidiobolus incongruus has been determined. Glucose and mannose were found to be the main sugars. The study of the ratio mannose/glucose has shown that there are 3 groups of strains. The first group which contains the strain of C. coronatus isolated from man or chimpanzee is characterized by a ratio lying between 0.92 and 1.3. The second group containing the strains of C. coronatus isolated from horse lesion or from soil is characterized by a ratio lying between 2.7 and 4.1. The last group which contains C. incongruus whose ratio mannose/glucose is 0.44. These results suggest the existence of two groups among the strains of C. coronatus. Lethal temperature of each strain and eventual presence of villosus spores are also mentioned.

     

Le Protoaurignacien : première culture de l'homme moderne de Provence et Ligurie

G. Laplace defined the Protoaurignacian in Liguria (“abri Mochi”) as the earliest occurrences of Upper Paleolithic in Italy. Stratigraphic sequences in Var exemplify that the Protoaurignacian is the first sequence of Upper Paleolithic in Provence and widely different from classic Aurignacian defined in southwestern France. Recorded in Languedoc-Roussillon, that one is documented in some other stratigraphic sequences from Monaco to southern Spain (“cueva del boquete de Zafarraya”). The Protoaurignacian argue that first modern humans arrived and occupied all along the Mediterranean coasts from Gibraltar to Toscana.     

Etude de quelques propriétés de la phosphofructokinase érythrocytaire de l'homme normal

Human erythrocyte phosphofructokinase was purified 150 fold by DEAE cellulose adsorption and ammonium sulfate precipitation.At pH 7,5 the enzyme exhibits allosteric kinetics with respect to ATP, fructose 6 phosphate, and Mg²⁺.ATP at high concentration acted as an inhibitor and ADP, 5′AMP, 3′,5′, AMP, acted as activators. Both effectors seemed to decrease the homotropic interactions beetween the fructose 6 phosphate molecules.The activators increased the affinity of phosphofructokinase for the substrate (F6P), the inhibitor decreased it.These ligands had no effect on the maximum velocity of the reaction except in the case of ADP.Interactions between the substrates and the effector ligands on the enzyme were considered in terms of the Monod - Changeux - Wyman model for allosteric proteins.With GTP and ITP, no inhibition was observed. At saturing concentration of GTP, ATP still inhibited phosphofructokinase.Both 3′5′ AMP and fructose 6 phosphate increased the concentration of ATP required to produce an inhibition of 50 %.Citrate, like ATP, inhibited phosphofructokinase by binding most likely at the same allosteric site. Erythrocyte phosphofructokinase is inhibited by 2–3 DPG.The study of the relation log V max = f (pH) suggested, that the active center contains at least one imidazole and one sulfhydryl group.     

Etude comparative d'activites enzymatiques microsomiques dans les hepatocytes de singe adulte et foetal: Comparative study of microsomal enzymic activities in adult and foetal monkey hepatocytes

Differential centrifugation was applied to adult and foetal liver of monkey. Obtained fractions were: F₁ (800 × g); F₂ (12 500 × g); F₃ (200 000 × g); and cell sap. Analysis of chemical compounds of these fractions shows that: (1) adult and foetal nucleic acids levels are similar; (2) there are more proteins in adult than in foetal hepatocytes; (3) most of the glycogen is located in F₃; the foetal level is twenty times higher than the adult level.Plasma membrane enzymes (5′-nucleotidase, adenylate cyclase) show a nucleomicrosomic distribution. The distribution of alkaline phosphatase is not significant.Mitochondrial enzymes (monoamine oxydase, succinate cytochrome c reductase, cytochrome oxydase) are enriched in F₂ without any sedimentation in F₃ There is more malate dehydrogenase liberated in cell sap during foetal liver fractionation. This indicates the foetal mitochondria are more sensitive to the homogenisation method.Lysosomal enzymes (acid phosphatase, N-acetylglucosaminidase) are enriched in F₂. The same observation for N-acetylglucosaminidase as for malate dehydrogenase leads to the same conclusion for foetal lysosomes.Endoplasmic reticulum and Golgi enzymes (glucose-6-phosphatase and related phosphotransferase activity, NADPH-cytochrome c reductase and sialyltransferase) are much enriched in F₃. Thus this fraction F₃ is pure enough to allow the observation of the modification produced on endoplasmic reticulum and Golgi apparatus during foetal and neonatal development.     

Over de verdeeling van de agglutininen over de serumeiwitten

Ohne Zusammenfassung Voordracht voor de Vergadering van de Ned. Ver. v. Microbiologie, gehouden te Utrecht op 12 November 1938. Uitvoerige publicatie met literatuur volgt in den vorm van een dissertatie.     

Essai de localisation subcellulaire de trois glycosyltransferases microsomiques de la muqueuse intestinale de rat

The present studies are concerned with the subcellular localisation of an active multiglycosyltransferase system involved in the transfer of galactose, N-acetylglucosamine and mannose to various glycoprotein acceptors. Smooth microsomes, obtained according to the method of Dallner, were the main loci of the three glycosyltransferases. After placing smooth microsomes in the bottom of a sucrose gradient, we recovered galactosyltransferase and mannosyltransferase in a fraction (density 1.12) containing Golgi apparatus and endoplasmic reticulum and N-acetylglucosaminyltransferase in a non-identified fraction with a density from 1.14 to 1.16; these results are obtained when performing all enzyme assays on endogenous acceptors. When exogenous acceptors was used, galactosyltransferase N-acetylglucosaminlytransferase and mannosyltransferase appear to be present in fractions having density of 1.14–1.16, 1.18 and 1.12, respectively.Un essai de localisation subcellulaire de trois glycosyltransferases présentes dans l'épithelium intestinal de rat est décrit. La caractérisation des diverses fractions obtenues est réalisée par le dosage d'enzymes marqueurs et par microscopic électronique.Dans le fractionnement selon la méthode de Dallner, les trois transférases: galactosyltransferase, N-acetylglucosaminyltransférase et mannosyltransferase sont présentes dans la fraction des membranes agranulaires.En gradient discontinu de saccharose, les activités endogènes de la galactosyltransferase, de la N-acetylglucosaminyltransférase et de la mannosyltransferase apparaissent dans des fractions de densité 1,12,1,15 et 1,12 respectivement. Dosés sur accepteur exogène, ces enzymes se répartissent préférentiellement dans les fractions de densité 1,12, 1,15 et 1,18 respectivement pour la mannosyltransferase, la galactosyltransferase et la N-acetylglucosaminyltransférase.     

Comparaison des modeles de neurone de Hodgkin-Huxley et de Nelson

Le modèle de Nelson peut-être considéré comme une approximation du modèle de Hodgkin-Huxley. Moins précis, il est plus maniable. Le modèle de Nelson peut également être considéré comme une généralisation du modèle de Hodgkin-Huxley. En effet, il introduit des liaisons synaptiques localisées ou diffusantes, et un processus de facilitation. Le mécanisme des liaisons synaptiques ne se traduit pas facilement dans le langage de Hodgkin-Huxley. Par contre, le processus de facilitation s'interprète facilement. Nelson's model can be taken as an approximation of Hodgkin-Huxley's model. Its precision is lesser, but it is more usable. Nelson's model can also be taken as a generalization of Hodgkin-Huxley's one; for it introduces localized or diffusing synaptic connexions and a facilitating process. The mechanism of synaptic connexions cannot be easily translated into Hodgkin-Huxley's language. On the contrary, the facilitating process is easily interpreted.