Pyruvate Fermentation by Oenococcus oeni and Leuconostoc mesenteroides and Role of Pyruvate Dehydrogenase in Anaerobic Fermentation

The heterofermentative lactic acid bacteria Oenococcus oeni and Leuconostoc mesenteroides are able to grow by fermentation of pyruvate as the carbon source (2 pyruvate → 1 lactate + 1 acetate + 1 CO₂). The growth yields amount to 4.0 and 5.3 g (dry weight)/mol of pyruvate, respectively, suggesting formation of 0.5 mol ATP/mol pyruvate. Pyruvate is oxidatively decarboxylated by pyruvate dehydrogenase to acetyl coenzyme A, which is then converted to acetate, yielding 1 mol of ATP. For NADH reoxidation, one further pyruvate molecule is reduced to lactate. The enzymes of the pathway were present after growth on pyruvate, and genome analysis showed the presence of the corresponding structural genes. The bacteria contain, in addition, pyruvate oxidase activity which is induced under microoxic conditions. Other homo- or heterofermentative lactic acid bacteria showed only low pyruvate fermentation activity.     

Association of Shiga toxin glycosphingolipid receptors with membrane microdomains of toxin-sensitive lymphoid and myeloid cells

Glycosphingolipids (GSLs) of the globo-series constitute specific receptors for Shiga toxins (Stxs) released by certain types of pathogenic Escherichia coli strains. Stx-loaded leukocytes may act as transporter cells in the blood and transfer the toxin to endothelial target cells. Therefore, we performed a thorough investigation on the expression of globo-series GSLs in serum-free cultivated Raji and Jurkat cells, representing B- and T-lymphocyte descendants, respectively, as well as THP-1 and HL-60 cells of the monocyte and granulocyte lineage, respectively. The presence of Stx-receptors in GSL preparations of Raji and THP-1 cells and the absence in Jurkat and HL-60 cells revealed high compliance of solid-phase immunodetection assays with the expression profiles of receptor-related glycosyltransferases, performed by qRT-PCR analysis, and Stx2-caused cellular damage. Canonical microdomain association of Stx GSL receptors, sphingomyelin, and cholesterol in membranes of Raji and THP-1 cells was assessed by comparative analysis of detergent-resistant membrane (DRM) and nonDRM fractions obtained by density gradient centrifugation and showed high correlation based on nonparametric statistical analysis. Our comprehensive study on the expression of Stx-receptors and their subcellular distribution provides the basis for exploring the functional role of lipid raft-associated Stx-receptors in cells of leukocyte origin.     

Seed dispersal strategies and the threat of defaunation in a Congo forest

Seed dispersal mode of plants and primary interactions with animals are studied in the evergreen Afrotropical forest of LuiKotale, at the south-western part of Salonga National Park (DR Congo). We first analysed seed dispersal strategies for (a) the plant species inventoried over a decade at the study site and (b) the tree community in 12 × 1 ha census plots. Our analyses of dispersal syndromes for 735 identified plant species show that 85 % produce fleshy fruits and rely on animals for primary seed dispersal. Trees depending on animals for primary dispersal dominate the tree community (95 %), while wind-dispersed and autochorous trees are rare in mixed tropical forests. A list of frugivorous vertebrate species of the ecosystem was established. Among the fruit-eating vertebrate species identified in the ecosystem, forest elephants and bonobos are threatened with extinction (IUCN, The IUCN red list of threatened species, 2012). Although most of the species listed previously are internationally and regionally protected, all the species we observed dispersing seeds are hunted, fished or trapped by humans in the area. With the exception of bush pigs, seed predators, mainly small-sized animals, are generally not targeted by hunters. As a consequence, we expect human pressure on key animal species to impact the plant community. We suggest defaunation to be considered as major conservation problem. Thus, not only for the sake of animal species but also for that of plant species conservation, anti-poaching measures should have priority in both “protected” and unprotected areas. Defaunation could bring a new impoverished era for plants in tropical forests.     

Three-Dimensional Protein Fold Determination from Backbone Amide Pseudocontact Shifts Generated by Lanthanide Tags at Multiple Sites

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Prospects for Bonobo Insectivory: Lui Kotal, Democratic Republic of Congo

Chimpanzees (Pan troglodytes) are well-known to eat invertebrates, especially social insects, across Africa, but allopatric bonobos (P. paniscus) are not. Bonobo insectivory is sparsely documented and apparently sporadic. However, the availability to bonobos of social insect prey and raw materials with which to make tools to exploit them is unknown. Here, we test a set of hypotheses that relates to questions of presence, abundance, density, and distribution of taxa that Pan consume and of vegetation suitable for making extractive foraging tools. We worked at Lui Kotal, Democratic Republic of Congo, where unprovisioned bonobos live in intact forest, far from villages. We collected insect and fecal specimens, transected for prey and assessed raw materials, and monitored mounds of Macrotermes. All but 1 of the major taxa of relevant termites, ants, and (stinging) honey bees were present. The 3 main taxa of insects that chimpanzees elsewhere eat —Macrotermes (fungus-growing termites), Dorylus (Anomma; army or driver ants), and Apis (honey bees)— were abundant and widespread, and usually at densities exceeding those at well-known chimpanzee study-sites. Similarly, woody and nonwoody vegetation suitable for making fishing probes was common at mounds of Macrotermes. There is no obvious ecological reason why bonobos should not use elementary technology in extractive foraging, e.g., termite-fish, ant-fish, ant-dip, honey-dip, to obtain social insects.     

The <Emphasis Type="Italic">Yersinia enterocolitica</Emphasis> type three secretion chaperone SycO is integrated into the Yop regulatory network and binds to the Yop secretion protein YscM1

Background  

Pathogenic yersiniae (Y. pestis, Y. pseudotuberculosis, Y. enterocolitica) share a virulence plasmid encoding a type three secretion system (T3SS). This T3SS comprises more than 40 constituents. Among these are the transport substrates called Yops (Yersinia outer proteins), the specific Yop chaperones (Sycs), and the Ysc (Yop secretion) proteins which form the transport machinery. The effectors YopO and YopP are encoded on an operon together with SycO, the chaperone of YopO. The characterization of SycO is the focus of this study.     

Der Zug des Sperbers(Accipiter nisus) auf Helgoland

Zusammenfassung Der Sperber ist auf Helgoland nur Durchzügler. Im langjährigen Mittel werden pro Jahr im Winter 0,4, auf dem Heimzug 2,1 und im Herbst 23,0 Fänglinge festgestellt. Der Zugablauf läßt eine Trennung der Zugzeiten der Alt- und Jungvögel einerseits sowie der und andererseits erkennen. Altvögel stellen 14,1%, 40,1% der Fänglinge. Anhand der Flügelmaße und Gewichte läßt sich mit fortschreitender Zugzeit keine klinale Variation nachweisen. Ältere Literaturangaben, Helgoland betreffend, werden teils korrigiert, teils präzisiert. Der geringe Anteil der Altvögel bzw. wird auf deren geringer ausgeprägten Zugtrieb zurückgeführt.

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The migration of the sparrow-hawk on Heligoland

Summary On Heligoland the Sparrow-Hawk occurs as a passage visitor only. Mean numbers (17 years) of birds trapped are 0.4 in winter, 2.1 during spring and 23.0 in autumn. Adults and juveniles as males and females as well show different periods of migration. Among birds trapped there are 14.1% adults and 40.1% females. No clinal variation of wing length and weight according to time of passage could be found. Former literature concerning Heligoland is partly corrected, partly rendered more precise. The low proportions of adults and females respectively are caused by weaker migratory urge.

     

Metabolism of polycyclic aromatic hydrocarbons in cultured human leukocytes under genetic control

Summary Metabolism of the polycyclic hydrocarbon benzo(a)pyrene(BP) to watersoluble products was measured in cultured human leukocytes from 35 healthy volunteers. The classification into 3 different groups with respect to degree of BP metabolism fits that obtained in a previous population and family study, where only the ratio of aryl hydrocarbon hydroxylase (AHH) activity of 3-methylcholanthrene (3MC) treated cultures to the activity of control cultures was measured. These data support previous observations that metabolism of polycyclic hydrocarbons is under genetic control.

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Zusammenfassung In der vorliegenden Arbeit wurde der Metabolismus des carcinogenen Kohlen wasserstoffes Benzpyren zu wasserlöslichen Produkten in Leukocytenkulturen von 35 gesunden Individuen untersucht. Hinsichtlich der Geschwindigkeit im Benzpyrenmetabolismus können 3 Gruppen unterschieden werden. Diese Einteilung ist in völliger Übereinstimmung mit der einer Populations-und Familienstudie, wo das Verhältnis der Aryl-Hydrocarbon-Hydroxylase-Aktivität von 3-Methylcholanthren-behandelten Leukocytenkulturen zu der von Kontrollkulturen bestimmt wurde. Diese Ergebnisse stützen die Beobachtung, daß der Metabolismus von carcinogenen Kohlenwasserstoffen unter genetischer Kontrolle ist.

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This work was supported in part by NIH Research Grant GM 15597 and Grant Ke 217/1 Deutsche Forschungsgemeinschaft (DFG).