Rapid Differentiation Between Nocardia and Streptomyces by Paper Chromatography of Whole-Cell Hydrolysates

Whole-cell hydrolysates were prepared from 58 strains of nocardiae and streptomycetes. Strains morphologically intermediate between the two genera and morphological variants of the same strains were included. Paper chromatograms made from the whole-cell hydrolysates clearly demonstrated meso-diaminopimelic acid as a major constituent of cultures of Nocardia spp., and LL-diaminopimelic acid as a major constituent of cultures of Streptomyces spp. In cultures of ten strains of N. madurae and of three of N. pelletieri, meso-diaminopimelic acid predominated, thereby supporting the assignment of these species to the genus Nocardia.     

Studies on the Hemolytic Properties of Protamine

The basic protein protamine causes a rapid hemolysis when incubated with the red blood cells of many mammalian species. The age of the cells does not affect the process. Neutralization of the active side groups of the protamine molecule with formalinization demonstrates that a specific degree of charge is necessary for hemolysis, as more than 30 per cent of the guanidine groups must remain unreacted to maintain activity. Unlike the hemolysis induced by the synthetic polypeptides polylysine and polyhomoarginine, protamine hemolysis is temperature-dependent. Whole lipoprotein material derived from red blood cell membranes inhibits protamine hemolysis to a greater extent than do the membranes themselves, serum, serum protein fractions, or cholesterol. The phosphatide and protein moieties derived from the membranes are quite avid in inhibiting protamine hemolysis. A probable explanation is that intracellular aggregation of these structural elements may cause changes in electrostatic charge and surface tension which result in increased permeability. The hemolytic and antitumor cell properties of protamine could not be segregated from its animal toxicity. Despite formalinization to a degree which eliminated the former, the compound remained quite toxic to mice and rabbits.     

Histochemical characteristics of chemoreceptor organs (Glomera)

Summary Some important histochemical characteristics of the carotid, aortic and coronary glomera have been studied in man and the rabbit.All glomera present a similar histochemical pattern. Type I glomus cells contain acetylcholinesterase, monoamine oxidase and norepinephrine. Type II glomus cells are highly positive for cholinesterase, carbonic anhydrase and nucleoside phosphatases hut they do not contain acetylcholinesterase nor catecholamines. It is postulated that the type I glomus cell is the true chemoreceptor cell. Together with the type II glomus cell, which is considered to be a special type of glial cell, a functional metabolic unit is established. Efferent nerve fibres could be adrenergic; by way of cholinergic transmission action potentials could be initiated in the afferent nerve fibres.The following Abbreviations will be used AChE acetylcholinesterase - ChE cholinesterase - iso-OMPA tetraisopropylpyrophosphoramide - DFP di-isopropylfluorophosphate - 62C47 15-bis-(4-trimethylammonium-phenyl) pentan-3-one-diiodide - CAH carbonic anhydrase - ATP-ase adenosine triphosphatase - NP-ases nucleoside phosphatases - UDP uridine diphosphate - UTP uridine triphosphate - IDP inosine diphosphate - CTP cytidine triphosphate - CaFoMa calcium-formol-macrodex - Glut glutaraldehyde - TPP-ase thiamine pyrophosphatase - MAO monoamine oxidase - CA catecholamines - NE norepinephrine     

Zur Blütenmorphologie und Bestäubungsökologie vonVeratrum album subsp.lobelianum (Bernh.)Rchb.

Zusammenfassung BeiVeratrum album subsp.lobelianum (Bernh.)Rchb. wurden im Gebirge Krkonoe (Riesengebirge) Blütenbau, Blütedauer und Blühverlauf studiert; besondere Berücksichtigung fanden dabei Vorkommen von Zwitterblüten und eingeschlechtlichen Blüten, Bau des Nektariums, Art und Weise der Nektarsekretion, Funktionsdauer der Narbe und Absinken der Keimfähigkeit des Pollens während der Anthese.Die Blütedauer der Zwitterblüten läßt eine deutliche Abhängigkeit von der Höhe ü. d. M. erkennen.Die (im Gegensatz zuVeratrum nigrum L.) weniger ausgeprägte Dichogamie erlaubt nur, ein männliches und ein Zwitterstadium der Blüte zu unterscheiden.Künstliche Bestäubungsversuche zeigten, daßV. album subsp.lobelianum weitgehend selbstfertil ist.Als regelmäßige Blumenbesucher und hauptsächlichste Bestäuber vonV. album susp.lobelianum wurden im obgenannten Gebirge 15 Dipteren-Arten (der Besucherzahl nach vorherrschend Aasfliegen) festgestellt, die ausgiebig Nachbar- und Fremdbestäubung (Geitonogamie, Allogamie), weniger schon Selbstbestäubung (Autogamie) bewirken.Die experimentelle Analyse des Blumenbesuches dieser Fliegen-Arten im Freiland ergab, daß ihre Fernanlockung durch den spezifischen Duft erfolgt, wobei die optische Wirkung der Blüten (Farbe, Form, Glanz der Nektarschicht) entbehrlich erscheint. Veratrum album susp.lobelianum kann bis zu einem gewissen Grade als aasblumig und ihre Blüte als Täuschblume bezeichnet werden.     

Das Verhalten von Ameisenarbeiterinnen gegenüber der Königin nach vorangegangener weisellosigkeit

Zusammenfassung Arbeiterinnen vonMyrmica ruginodis Nyl. werden im weisellosen Zustand fertil. Sie legen aber keine Eier, wenn sie mehr als 3 Larven je Arbeiterin zu versorgen haben (Mamsch, 1965). Arbeiterinnengruppen wurden mit und ohne Larven von der Königin abgetrennt. In den eierlegenden Gruppen wurde die erneut zugesetzte eigene Königin entweder nicht beachtet oder angegriffen. In den Gruppen, in denen die Arbeiterinnen durch Larvenpflege unfruchtbar blieben, wurde die Königin intensiv beleckt und in das engere Nest eingetragen. Isolierte eierlegende Arbeitergruppen zeigten im Gegensatz zu Arbeiterinnen mit inaktiven Ovarien keine Tendenz, sich mit der Königingruppe zu vereinigen. Das veränderte Verhalten der Arbeiterinnen gegenüber der Königin ist demnach nicht vom Zeitraum der Weisellosigkeit abhängig. Es wurde nur bei eierlegenden Arbeiterinnen beobachtet.

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Summary Workers ofMyrmica ruginodis Nyl. start laying eggs after being separated from their queen. No deposition of eggs occurs in groups in which each worker has to feed 3 or more larvae (Mamsch, 1965). Worker groups rearing larvae and those without brood were separated from the queen.When the queen was put again into an egg-laying worker group, either no attention was paid to her or she was attacked. In groups of workers sterile due to rearing larvae the queen was licked intensively and carried into the nest cavity. Fertile worker groups showed no tendency to join the queen group. The change in the workers' behaviour does not depend on the time of the separation from the queen. It only occurs in groups of fertile workers.

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Résumé Des ouvrières deMyrmica ruginodis Nyl. deviennent fertiles après avoir été séparées de la reine. Mais elles ne pondent pas d'ufs, si elles ont chacune trois larves ou plus à nourrir (Mamsch, 1965). Des groupes d'ouvrières, d'une part avec larves et d'autre part sans, ont été séparés de la reine. Les groupes d'ouvrières pondeuses n'attachaient pas d'attention à la reine replacée dans le nid ou encore l'attaquaient. Dans les groupes où les ouvrières étaient restées infertiles à cause du nourrissement du couvain, la reine était léchée d'une façon intensive et portée à l'intérieur du nid. A l'opposé des ouvrières stériles, les groupes d'ouvrières pondeuses isolées ne montraient aucune tendance à joindre le groupe de la reine. Le changement du comportement des ouvrières ne dépend donc pas de la durée de l'état orphelin; il n'est observé que chez les ouvrières pondeuses.

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Herrn Prof. Dr.K. Gösswald, zum 60. Geburtstag gewidmet.     

Die Ultrastruktur der Kapillarwand in der menschlichen Placenta zur Zeit der Schwangerschaftsmitte

Zusammenfassung Die Wand der Kapillaren in der menschlichen Placenta aus der Schwangerschaftsmitte wird elektronenmikroskopisch untersucht und zu der Wand des Sinusoides der reifen Placenta in Beziehung gesetzt. Bereits zur Zeit der Schwangerschaftsmitte sind vereinzelt Sinusoide nachweisbar, doch treten sie gegenüber den Kapillaren zahlenmäßig in den Hintergrund.Die Kapillaren des Zottenbinnenraumes besitzen keine Basalmembran; sie sitzen meist, nur durch einen Spalt getrennt, einer Pericytenschicht auf. Die Pericyten haben häufig fußförmige Ausläufer, die die Basalmembran des Cytotrophoblasten erreichen. Die Kapillarendothelien sind zwar einreihig angeordnet, überlappen aber einander in ausgedehnter Weise.Im Cytoplasma der Kapillarendothelien findet man häufig eine feinfilamentäre Zeichnung, jedoch nur nach Kaliumpermanganat-Kontrastierung.Die Kapillaren der unreifen Placenta sind durch das Fehlen der Basalmembran, durch die ungewöhnliche Dicke und durch die starke Überlappung ihres Endothels für eine Gefügedilatation besonders geeignet.Mit Unterstützung durch die Deutsche Forschungsgemeinschaft.     

Rearrangement of VHa1-encoding Ig gene segment to the a2 chromosome in an a1/a2 heterozygous rabbit. Evidence for trans recombination

VDJ genes were cloned from leukemic B cells of an a1/a2 heterozygous Emu-cmyc transgenic rabbit. Restriction mapping and nucleotide sequence analysis indicated that one clone, 5C3, had a VHa1-encoding gene segment functionally rearranged to a JH gene segment from the a2 chromosome. This VDJ gene may be the result of a trans recombination between a VH gene on the a1 chromosome and a JH gene segment on the a2 chromosome or, it may be the result of a cis recombination if the a2 chromosome contains VHa1-encoding gene segments.     

Lectin binding to cells of Schistosoma mansoni sporocysts and surrounding Biomphalaria glabrata tissue

The binding of different lectins to the surface of mother and daughter sporocysts of Schistosoma mansoni (Trematoda) and to cells of its intermediate host Biomphalaria glabrata (Gastropoda) was investigated. The test system consisted of several biotin-labeled lectins, an avidin-biotin-peroxidase complex and 3,3'-diaminobenzidine. The fixatives used were Formalin, Bouin's and Zenker's solutions; unfixed material was also studied. Most lectins reacted equally with host tissue and parasite tissue. However, receptors for Ulex europaeus I (most probably fucose) were only demonstrated on daughter sporocysts. Thus, a method was found to specifically mark Schistosoma mansoni daughter sporocysts in the digestive gland tissue of its intermediate host. Mother sporocysts and surrounding host tissue differed in their distribution of galactosyl groups. Both lack fucose and N-acetyl-galactosamine. The differences in lectin binding of galactosyl determinants were also observed during the in vitro development of mother to daughter sporocysts.     

Origin of ultraviolet damage in DNA

A novel ultraviolet (u.v.) footprinting technique has been used to analyze the formation of u.v. photoproducts at 250 bases of a 5 S rRNA gene under conditions where the gene is either double or single-stranded. Because many more types of u.v. damage can be detected by the u.v. footprinting technique than has been previously possible, we have been able to examine in detail why certain bases in DNA are damaged by u.v. light while others are not. Our measurements demonstrate that the ability of u.v. light to damage a given base in DNA is determined by two factors, the sequence of the DNA in the immediate vicinity of the photoproduct, and the flexibility of the DNA at the site of the photoproduct. For pyrimidines, the predominant photoreaction in double-stranded DNA involves covalent dimerization between adjacent pyrimidine residues. Dimerization is much easier in melted DNA because the geometrical changes required for adjacent pyrimidine residues to dimerize are easier in single-stranded DNA. The absorption of a u.v. photon cannot simultaneously induce the geometrical changes required for adjacent pyrimidines or other bases to dimerize with one another. Rather, upon the absorption of a u.v. photon, only those thermally excited bases that are in a geometry capable of easily forming a photodimer during excitation, can photoreact. In contrast to adjacent pyrimidines, non-adjacent pyrimidines (pyrimidines flanked on either side by a purine) do not readily form u.v. photoproducts in double-stranded DNA. Because photoreactions at non-adjacent pyrimidine residues are greatly enhanced in single-stranded DNA, their failure to form in double-helical DNA is attributed to torsional constraints imposed by the double helix which make it difficult for non-adjacent pyrimidines to adopt a geometry necessary for photoreaction. Although purines are believed to be resistant to u.v. damage, our measurements demonstrate that at moderate u.v. dosages purines which are flanked on their 5' side by two or more contiguous pyrimidines readily form u.v. photoproducts in double-stranded DNA. Flanking pyrimidines appear to activate purine photoreactions by transferring triplet excitation energy to the purine. Melting of the DNA helix greatly inhibits the ability of flanking pyrimidines to activate purine photoreactions, presumably by disrupting intimate orbital overlap required for triplet transfer.