Isolation of (−)-cryptosporiopsin,a chlorinated cyclopentenone fungitoxic metabolite fromPhialophora asteris f. sp.helianthi

Summary The (–)-enantiomer of cryptosporiopsin, a chlorinated cyclopentenone fungitoxic metabolite, was isolated fromPhialophora asteris f. sp.helianthi. Next to a comparable fungitoxic activity as shown by crypstosporiopsin, the product particularly inhibits growth ofSclerotinia sclerotiorum, an important pathogen on sunflower. Two further metabolites were tentatively identified as a stereoisomer of cryptosporiopsin and its dehydrated derivative.The authors are much indebted to Dr.G. M. Strunz (Canadian Forestry Service) for valuable suggestions and the generous gift of cryptosporiopsin and to the University of Utrecht for the part-time fellowship to one of us (Y.T.) given.     

On short adrenergic neurons in the accessory male genital organs of the bull

Zusammenfassung Basierend auf dem speziellen Betragen der isolierten Noradrenalingranula der inneren männlichen Geschlechtsdrüsen, die von kurzen adrenergischen Neuronen innerviert sind, werden Definitionen für 4 «übergangsformen» der peripheren katecholamin-enthaltenden Zellen diskutiert: chromaffine Zellen der Adrenomedulla, kleine verzweigte, nicht adrenale chromaffine Zellen,kurze adrenergische Neurone undlange adrenergische Neurone.     

Cytological demonstration of female heterogamety in isopods

Résumé Des chromosomes sexuels, inconnus jusqu'à présent chez les Isopodes, ont été trouvés dans 4 espèces de la superespèceJaera marina (Janiridae, Asellota). Il s'agit d'un système multiple de chromosomes sexuels, ce qui aboutit à la formation d'un trivalent sexuel dans la méiose femelle. Les femelles — hétérogamétiques — ont la constitution XY₁Y₂, les mâles étant XX. D'après les données chromosomiques présentées par les 4 espèces étudiées, la formation du système multiple sexuel est due à des processus cytologiques évolutifs d'ordre Robertsonien.

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Aided by a grant from the Janggen Pöhn Foundation (St. Gallen, Switzerland) and supported by the Swiss Commission for the Biological Station of Roscoff.     

Affinity chromatography of monoamine oxidase

Summary A method is described for the purification of pig liver monoamine oxidase by affinity chromatography, using a colum with covalently bound pargyline.Acknowledgment. The authors wish to thank the University Research Council for financial support.     

Strain difference in sex ratio response of mice to lactate dehydrogenase virus infection

Zusammenfassung Durch Infektion mit LDH-Virus wird bei Mäusen, deren Nachkommen normalerweise ein Geschlechtsverhältnis <1 aufweisen, ein solches von 1 erreicht. Da sich die Infektion der Eltern beider Stämme nicht in einer unterschiedlichen Zunahme der Serum-LDH, wohl aber in einer solchen der Spermien-LDH auswirkt, wird angenommen, dass die LDH-Aktivität der Spermien sich in einer zwar noch unbekannten Weise auf das Geschlechtsverhältnis der Nachkommen auswirkt.

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Supported by a grant from the Maryland Division of the American Cancer Society.     

Compte rendu des publications

Cellular and Molecular Life Sciences -     

Nouveaux livres

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The structure of amoorastatone and the cytotoxic limonoid 12-hydroxyamoorastatin

Summary 2 new limonoid-type terpenes have been isolated from an aqueous extract of seeds produced by the Eastern Himalayan (India) plantAphanamixis grandifolia Bl. By interpreting principally mass spectral and nuclear magnetic resonance data, the structures of 12-hydroxyamoorastatin (2b) and amoorastatone (3) were elucidated. Unequivocal evidence for the 12-hydroxyamoorastatin structural assignment was obtained by chemical conversion to sendanin (4). Amoorastatin derivative2b was found to significantly inhibit growth of the murine P388 lymphocytic leukemia cell lines but amoorastatone in the same system was inactive. In a comparative biological study, sendanin (4) and anthothecol (7) were also found significantly to inhibit growth of the P388 cell line, while rohitukin (8) and limonin (9) were found to be inactive.Part 63 of the series Antineoplastic Agents. For the previous contribution refer to G.R. Pettit, T.S. Krupa and R.M. Reynolds, Int. J. Peptide Protein Res., in preparation. The present investigation was supported in part by Public Health Research Grant No. CA-16049-05 from the National Cancer Institute, the Fannie E. Rippel Foundation, Mrs Mary Dell Pritzlaff, the Spencer T. and Ann W. Olin Foundation, Mr John F. Schmidt, and the Phoenix Coca-Cola Bottling Company.