Isolation and identification of spirorenone metabolites from the monkey (Macaca fascicularis)

The plasma level of spirorenone was determined 3 h after 1, 8, 22 and 46 daily oral administrations of 20 mg/kg to two female and two male monkeys ($\text{Macaca fascicularis}$). A fifth animal, female, was treated with eight daily doses of tritium-labelled drug and was completely bled from the carotid vein 4 h after the last administration in order to isolate and identify plasma metabolites.After repeated daily doses of spirorenone the mean plasma level of unchanged drug was 711 ± 213 ng/ml. In the plasma of the fifth animal four radioactively labelled compounds could be detected after extraction and subsequent HPLC separation. Mass spectrometric identification of three of the substances indicated 1,2-dihydrospirorenone, hydroxy-1,2-dihydrospirorenone and the unchanged drug itself.     

Electrophoretic and biochemical studies of human aldehyde dehydrogenase isozymes in various tissues

Four major ALDH isozymes have been identified in human tissues using starch gel electrophoresis and isoelectric focusing. The isozyme bands have been termed as ALDH I, II, III and IV according to their decreasing electrophoretic migration and increasing isoelectric point. The isozymes have been partially purified via preparative isoelectric focusing. Kinetic characteristics of ALDH I and II were found to be quite similar to ALDH enzyme 2 and enzyme 1 described earlier by Greenfield and Pietruszko (Biochem Biophys Acta, $\text{483}$ 35–45 1977). ALDH III and IV showed a very high Km for propionaldehyde (1.0–1.5 mM at pH 9.5) and were not inhibited by disulfiram at pH 9.5. A variant phenotype of ALDH which lacked in isozyme I was detected in various tissues from Japanese individuals. Comparative kinetic properties of normal and variant enzyme are given.     

The metabolic interactions between Paramecium bursaria Ehrbg. and Chlorella spec. in the Paramecium bursaria-symbiosis

In an organism (strain C 1/2 from Dr. P. R. Hayes, Leeds) regarded as a typical representative of the genus Flavobacterium, flexirubin-type pigments have been identified. The Flavobacterium pigments contain structural elements of both, the pigments of the genus Flexibacter and the pigments of the genus Cytophaga. As flexirubin-type pigments seem to have a rather restricted distribution among bacteria, and have formerly proved to be useful chemosystematic markers for the flexibacteria, this new observation may indicate that there is a relatively close phylogenetic relationship between this type of flavobacteria and the Cytophaga-Flexibacter group.     

A fast and simple radiometric assay for adenosine deaminase using reversed-phase thin-layer chromatography

A new quantitative radiometric assay for adenosine deaminase is described. The reaction conditions are similar to those used in other radioassays and are shown to result in an activity which increases linearly with time and with enzyme concentration. An original feature of the technique resides in the use of reversed-phase thin-layer chromatography to separate adenosine from inosine. The separation is complete, fast, and reproducible. Both compounds can be recovered almost quantitatively from the plates. The assay is very simple and allows the determination of up to 36 samples in 3 h.     

Ferritin as an exogenous yolk protein in snails

Summary A main yolk component in the oocytes of the pulmonate snailPlanorbarius corneus L. has been isolated and identified as the iron storage protein ferritin by its ultrastructure, iron content, immuunological properties and behaviour in disc electrophoresis. As judged from acrylamide electrophoresis data and ultrastructural observations, yolk ferritin is an exogenous protein which is synthesised in the hepatopancreas and taken up by the oocytes by endocytosis.     

Entwicklung und Bau der Doppelspermien bei den DytiscidenAcilius sulcatus L.,Dytiscus marginalis L. undHydaticus transversalis Pont. (Coleoptera)

Zusammenfassung BeiAcilius sulcatus undDytiscus marginalis wurde die Spermiogenese bis zu den reifen Doppelspermien, beiHydaticus transversalis wurden nur die reifen Doppelspermien untersucht. Die Konjugation der Spermien dieser Arten erfolgt als letzter Schritt erst im distalen Teil des Hodenausführungsganges. Voraussetzungen für ihr Zustandekommen sind sowohl lokale Differenzierungen der Spermienmembran, alsauch spezifische polysaccharidhaltige Beläge, von denen nach dem Aussehen sowie nach Zeitpunkt und Ort ihres Auftretens vier unterschieden werden können, die teils schon im Zystenlumen, teils erst nach Eindringen des Spermienvorderendes in tiefe Fächer der Zystenwandzellen gebildet werden. Die mit allen Belägen versehenen Einzelspermien treten zusammen mit abgeschnürten Resten der Zystenwandzellen in den Ausführungsgang ein, dessen Epithel die Plasmareste der Zystenwandzellen phagozytiert. Die Beläge der Spermien sind nach der Konjugation verändert. Damit muß als letzte Bedingung für das Zustandekommen des Aneinanderhaftens noch eine Reaktion im Ausführungsgang stattfinden. Weiterhin wurde die Entwicklung des als microtubular border beschriebenen Strukturelements im Schwanz verfolgt und als centriole adjunct identifiziert, welches sich aus Kernmaterial herleitet und zu einem Geißelbegleitkörper modifiziert hat. Schließlich wird auf anscheinend regelmäßige und in zeitlich abgestimmter Folge auftretende Beziehungen des Endomembransystems zu den sich differenzierenden Strukturen der Spermatide hingewiesen.

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Development and structure of the conjugate sperm of the dytiscidaeAcilius sulcatus L.,Dytiscus marginalis L. andHydaticus transversalis pont. (Coleoptera)

Summary Spermiogenesis and structure of the double sperm have been investigated inAcilius sulcatus andDytiscus marginalis whereas only mature double sperm have been studied inHydaticus transversalis. The conjugation of the sperm in these species is accomplished as a last step in the distal part of the vas deferens. Preconditions for the pairing are local differentiations of the sperm membrane in combination with specific layers of polysaccharids. According to their aspect as well as the chronological order and place of their appearance four such layers can be discerned. These are formed in part still in the lumen of the cyst, in part not earlier than after the anterior ends of the sperm have deeply entered into recesses of the surrounding cyst wall cells. Single sperm supplied with all layers and cytoplasmic remnants pinched off from the cyst wall cells enter the vas deferens where the cytoplasmic remainders are phagocytised by its epithelial cells. The layers of the sperm are transformed after conjugation. Thus as a last precondition for the occurrance of pairing a reaction in the vas deferens must take place. Furthermore, the development of the structural element of the tail described as microtubular border has been traced and identified as a centriole adjunct derived from nuclear material and modified to a body accompanying the flagellum. Finally, it is pointed out that apparently regular relationships in temporally correlated sequence exist between the endomembranous system and differentiating structures of the spermatid.

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Mit Unterstützung durch die Deutsche Forschungsgemeinschaft.

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För die rasterelektronenmikroskopischen Aufnahmen der Abb. 9 danke ich Frau L. Schulz, Homburg, verbindlichst. Die Teilbilder 16g u. h konnten mit einem Siemens Elmiskop 102 aufgenommen werden. För die Anfertigung dieser Aufnahmen bin ich Frau Dr. C. Weichan, Berlin, zu Dank verpflichtet.     

A special class of nonlinear interactions in the visual system of the fly

Flies can detect a small object in front of a randomly contrasted background if the object undergoes small motions. The effect was investigated in fixed flying flies under open-loop conditions. The results suggest that nonlinear inhibitory interactions underly this elementary case of figure-ground discrimination.     

Esterase-D polymorphism in Assam by cellulose acetate electrophoresis

Summary With the help of a simplifed and quick method, cellulose acetate electrophoresis, the phenotypes of esterase D were determined in an Assamese population. The gene frequencies of Es D¹ were 0.7263 and 0.2737 for Es D².

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Zusammenfassung In einer Stichprobe aus Assam wurde mit Hilfe einer einfachen und schnellen Methode, der Cellulose-Acetat-Elektrophorese, die Bestimmung der Esterase D-Phänotypen durchgeführt. Die Genfrequenzen wurden für Es D¹ zu 0,.7263 und für Es D² zu 0.2737 bestimmt.

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Supported by the Deutsche Forschungsgemeinschaft, the Stiftung VW and the Fonds der Chemischen Industries.