Enzymic properties of intestinal aminopeptidase P: a new continuous assay

A continuous photometric assay of aminopeptidase P activity was developed which is based on a coupled enzymic assay with the substrate Gly-Pro-Pro-pNA and DPP IV as auxiliary enzyme. This assay was used to evaluate the kinetic parameters and inhibitory profile of intestinal brush border aminopeptidase P.     

Localization of a highly immunogenic region on the acetylcholine receptor alpha-subunit

Antibodies to synthetic peptides were employed in order to map domains on the alpha-subunit of the acetylcholine receptor to which several monoclonal antibodies are directed. Five peptides corresponding to residues 1-20, 126-143, 169-181, 330-340 and 351-368 of the receptor alpha-subunit were synthesized and antibodies against them were elicited. The anti-peptide antibodies were employed along with the monoclonal antibodies to identify fragments of S. aureus V8 protease digested- alpha-subunit in immunoblotting experiments. Our results demonstrate that a highly immunogenic region of the alpha-subunit is located on a carboxy-terminal 14 kDa portion of the alpha-subunit. This region also seems to undergo antigenic changes during muscle development. A monoclonal antibody directed against the cholinergic binding site of the acetylcholine receptor reacted with an 18 kDa segment of the alpha-subunit which bound alpha-bungarotoxin as well as antibodies directed against peptide 169-181.     

NMR, CD and IR spectroscopies of a tridecanucleotide containing a no-base residue: coexistence of B and Z conformations.

The synthesis of the tridecadeoxynucleotide d(CGm5CGCGxACATGT), where x is the 1-cyano-2-deoxy-beta-D-erythropentofuranose, is described. The NMR, IR, CD studies at various salt concentrations and temperatures of this oligomer show that the B and Z conformations are simultaneously present in the same short DNA fragment. A single apurinic residue is sufficient for the coexistence of the B and Z helices on this oligomer.     

Epidermal ultrastructure of Anoplodium stichopi (Plathelminthes,Dalyellioida), a flatworm endosymbiotic in Stichopus tremulus (Holothurioida)

Summary The epidermal ultrastructure of Anoplodium stichopi Bock 1925 (Platyhelminthes, Dalyellioida, Umagillidae) was studied using transmission and scanning electron microscopy. The species lives in the perivisceral coelom of the aspidochirote holothurian Stichopus tremulus Gunnerus 1767. Two types of cells were observed in the epidermis of A. stichopi: ciliated cuboidal epithelial cells and nonciliated pear-shaped cells. The surface of the ciliated epidermal cells is folded into anastomosing ridges. Numerous coated vesicles are subjacent to the surface folds and mitochondria are abundant just below them. Observations indicate that A. stichopi takes up nutrients pinocytically from the coelomic fluid of the host. The ciliation of A. stichopi is sparse.     

The incorporation of selenium and alterations of macro- and trace element levels in individual blood cells following supplementation with sodium selenite and vitamin E

Significant alterations in the selenium content of erythrocytes, thrombocytes, and neutrophil granulocytes were observed following a daily supplementation of 200 μg Se + 100 mg vitamin E during a period of 2 months. The neutrophil granulocytes incorporated more selenium than the thrombocytes. The iron content of the thrombocytes decreased on selenium supplementation, while the opposite was noted for the neutrophil granulocytes. The glutathione peroxidase activity was not significantly changed during the period of observation.     

Eine nicht-reziproke Kreuzungssterilität zwischen ökologischen Rassen der Mücke Clunio marinus

Zusammenfassung Die in der Gezeitenzone lebende Mücke Clunio marinus ist längs der europäischen Küstenlinie verbreitet. Die experimentell geprüften Stämme verschiedener geographischer Herkunft repräsentieren ökologische Rassen, die sich in der zeitlichen Programmierung ihrer Entwicklung unterscheiden. Es wurde die Kreuzbarkeit zwischen insgesamt 7 Stämmen geprüft.Zwischen einzelnen Stämmen wurde eine nicht-reziproke Kreuzungssterilität (abgekürzt n.r.St.) nachgewiesen, bei der jeweils in einer Kreuzungsrichtung fertile Nachkommen entstanden und in der reziproken Kreuzung Nachkommen fehlten.Die Vererbung der n.r.St. wurde zwischen 2 Stämmen benachbarter Rassen mit der Methode der wiederholten Rückkreuzung geprüft. Es ergab sich ein matrokliner Erbgang. Die Befunde werden mit entsprechenden Ergebnissen von Laven an Culex pipiens verglichen.Die populationsgenetischen Konsequenzen der n.r.St. werden in Hinblick auf die Elimination von Kreuzungstypen, Genfluß und reproduktive Isolation betrachtet. Für die Bedeutung der n.r.St. im Freiland werden 3 Hypothesen erörtert: 1. Begleiterscheinung der genetisch divergierenden Rassen, 2. in einer Richtung wirksamer Isolationsmechanismus zwischen benachbarten Rassen und 3. Speciation.

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Summary The intertidal midge Clunio marinus is distributed along the European coast-line. Stocks from distinct locations differ in the programming of their emergence time. They represent ecological races. The crossability between 7 stocks was examined.Between some stocks a non-reciprocal cross sterility has been found, characterized by fertile hybrids in one cross direction, and no offspring in the reciprocal crosses.The cross Jean xSan was fertile, while the cross San xJean was sterile. After three backcrosses of the hybrid females to San males, the sterility in the reciprocal crosses with San females had not been changed. The maternal inheritance of this non-reciprocal sterility is compared with similar studies in Culex pipiens by Laven.According to aspects of population genetics, the non-reciprocal cross sterility is considered in view of elimination of crossing types, of gene flow and reproductive isolation. With regard to the significance of the non-reciprocal cross sterility in the field, three hypotheses are discussed: 1. by-product of evolutionary divergence in ecological races, 2. unilateral reproductive isolation which blocks the gene flow between adjacent populations only in one direction, and 3. speciation.

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Mit Unterstützung durch die Deutsche Forschungsgemeinschaft.

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Herrn Professor Dr. Gerhard Krause zu seinem 65. Geburtstag.     

Degradation of heparin in mouse mastocytoma tissue

1. Heparin was prepared from mouse mastocytoma tissue by mild procedures, including extraction of mast-cell granules with 2m-potassium chloride, precipitation of the extracted polysaccharide with cetylpyridinium chloride from 0.8m-potassium chloride and finally digestion of the isolated material with testicular hyaluronidase. The resulting product (fraction GE(H)) represented approx. 40% of the total heparin content of the tissue. 2. Fraction GE(H) was fractionated by gel chromatography on Sepharose 4B into three subfractions, with average molecular weights ( M(w)) of approx. 60000-70000 (highly polydisperse material), 26000 and 9000 respectively. Treatment of each of the subfractions with alkali or with papain did not affect their behaviour on gel chromatography. Amino acid and neutral sugar analyses indicated that the two low-molecular-weight fractions consisted largely of single polysaccharide chains lacking the carbohydrate-protein linkage region. It was suggested that these heparin molecules had been degraded by an endopolysaccharidase. 3. Pulse labelling in vivo of mastocytoma heparin with [(35)S]sulphate showed initial labelling of large molecules followed by a progressive shift of radioactivity toward fractions of lower molecular weight. Further, heparin-depolymerizing activity was demonstrated by incubating (35)S-labelled heparin in vitro with a mastocytoma 10000g-supernatant fraction. Appreciable degradation of the polysaccharide occurred, as demonstrated by gel chromatography. In contrast, no depolymerization was observed on subjecting (14)C-labelled chondroitin sulphate to the same procedure.     

The distribution of sulphate residues in the chondroitin sulphate chain

1. Electrophoresis of chondroitin sulphate, before and after partial degradation with testicular hyaluronidase, revealed charge heterogeneity of the degraded but not of the intact polymer. 2. Hyaluronidase-treated chondroitin sulphate was fractionated by gel chromatography. Two subfractions which were essentially monodisperse with regard to molecular weight (values of 8600 and 4800, respectively) were separated further by chromatography on Dowex 1. The resulting subfractions differed considerably with respect to their sulphate/disaccharide molar ratios. 3. Amino acid and neutral-sugar analyses of the Dowex 1 subfractions showed that the less sulphated fragments contained the carbohydrate-protein linkage region, whereas the high-sulphated fragments essentially lacked this constituent. It was concluded that chondroitin sulphate contains relatively less sulphate in the vicinity of the carbohydrate-protein linkage region than in the more peripheral portion of the polysaccharide chain.