Wirkungen von L-glutaminsäure auf grösse und puff-muster der Larvalen Speicheldrüsenchromosomen von Drosophila melanogaster in vivo

The ratio DNA: RNA in the dry substance of Drosophila melanogaster larvae changes when L-glutamic acid is added to the substratum. The number of cells in the salivary glands is not affected (Fahrig et al., 1967). The present paper deals with the effect of this altered ratio on the puffing pattern of the salivary gland chromosomes.Compared to controls of the same game age, glutamic acid fed prepupae younger than 15 min have five additional puffs. In all, 98 pairs of homologous puffs were studied. In 54 of these, size differences were tested statistically; in the glutamic acid series, 20 puffs were larger and 18 smaller than in the controls whereas 16 had the same size. Size reduction was stronger in the more prominent puffs. In prepupae reared at lower temperatures, chromosomes were significantly longer. Glutamic acid causes a significant increase in chromosome width. Combined measurements of both effects were made by determining the surface area of tested segments. Lowering the temperature adds higher size classes, whereas addition of glutamic acid causes a significant shift of the distributional peak towards the higher size classes. This excludes the possibility of an additional replication cycle. In salivary glands of glutamic acid fed prepupae the majority of nuclei have reached the highest degree of polyteny, which in controls is never found at 25° C but sometimes at 18° C. The agent causing both additional puffing and enhanced growth is effective only via the alimentary tract of the larva.     

Catabolism of flavonol glucosides in plant cell suspension cultures

Catabolism of flavonol glucosides was investigated in plant cell suspension cultures using kaempferol 3-O-β-d-glucoside and kaempferol 7-O-β-d-glucoside labelled with ¹⁴C either in the glucose or in the flavonol moiety. Catabolic rates of glucosides were compared with those of free glucose and kaempferol. All substrates were degraded efficiently by cell cultures of mungbean, soybean, garbanzo bean and parsley. Based on ¹⁴CO₂-formation, glucose from position 3 of kaempferol is 3–5 times more rapidly metabolized than that from position 7. The flavonol nucleus from both isomers is, however, oxidized to the same extent with a considerable portion of the flavonol being incorporated into insoluble polymeric cell material.     

Photosynthetischer Elektronentransport der Alge Bumilleriopsis während der Zellentwicklung

Summary The alga Bumilleriopsis filiformis Vischer (Xanthophyceae) was synchronized by light intensity combined with temperature changes. During the 48-h cell cycle there is a stage of low cellular photosynthetic activity in the 34th hour after start of the cycle and one of high activity between the 39th and 41th hour. These activities were compared with the p-benzoquinone mediated Hill reaction of non-homogenized cells and electron transport rates measured with carefully isolated chloroplast material. Ferricyanide and methylviologen reduction was tested with water as donor and photosystem I reactions with reduced dichloro-phenolindophenol and diaminodurene. The influence of superoxide dismutase and ascorbate was examined. The data show parallel changes in the activities of electron transport and cellular photosynthesis during cell development and indicate corresponding alteration not only in the activity of photosystem II but also in that of system I.

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Abkürzungen pBQ p-Benzochinon - Chl Chlorophyll - DAD 2,3,5,6-Tetramethyl-p-phenylendiamin (Diaminodurol) - DCMU 3-(3,4-Dichlorphenyl)-1,1-dimethylharnstoff - DCIP 2,6-Dichlorphenolindophenol - FCCP Carbonylcyanid-p-trifluormethoxyphenyl-hydrazon - FeCy Kaliumhexacyano-(III)-ferrat - LST (Stark)-Licht-Schwachlicht-Temperaturwechsel (zur Synchronisierung) - MV Methylviologen (1,1-Dimethyl-4,4-dipyridylium-dichlorid) - PS-I, PS-II Photosystem I bzw, II - SOD Superoxid-Dismutase - TRICIN N-Tris-(hydroxymethyl)-methylglycin (Puffer)     

The estimation of phenylalanine ammonia-lyase (PAL)-activity in intact cells of higher plant tissue

From cell cultures of Haplopappus gracilis, an enzyme, catalyzing the glucosylation of cyanidin at the 3 position using uridine diphosphate-D-glucose (UDPG) as glucosyl-donor, has been isolated and purified 50-fold. The enzyme was not specific for cyanidin alone, but also glucosylated other anthocyanidins and flavonols in position 3. However, apigenin, luteolin, naringenin and dihydroquercetin were not glucosylated. The reaction has an optimum pH of approximately 8, and the apparent K _m values for UDPG and cyanidin were 0.5 and 0.33 mM respectively. The enzyme reaction is strongly inhibited by cyanidin (above 0.25 mM).     

Strukturelle Grundlagen des Parasitismus beiOrobanche III. Die Differenzierung des Xylemanschlusses beiO. crenata

Zusammenfassung Innerhalb des Wirtsxylems wurden Haustorialzellen des WurzelparasitenOrobanche lichtund elektronenoptisch untersucht. Diese Zellen durchlaufen eine ungewöhnliche Differenzierung bis sie wasserleitendes Xylemanschlu\element sind. Von Haustorialzellen mit stark verdickten FrontwÄnden entwickeln sie sich bei Eintritt in das Wirtsxylem zu einer typischen Transferzelle mit polar zum Holzelement des Wirts angelegtem Wandlabyrinth. Erst durch einen zweiten Differenzierungsschritt wird die Transferzelle zum Wasserleitelement, indem die typischen SekundÄrwandverdickungen des Xylems in der Zelle angelegt werden. Diese entstehen teilweise innerhalb des Wandlabyrinths und sind stets gegenüber denjenigen des Wirtselements angelegt. Zuletzt wird das Labyrinth — bis auf gelegentliche Reststrukturen — abgebaut, der Protoplast degeneriert, und es entsteht ein haustoriales Wasserleitelement, das über kommunizierende Tüpfel an das Wirtselement angeschlossen ist.

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Structural features of parasitism ofOrobanche III. The differentiation of xylem connexion ofO. crenata

Summary Haustorial cells of the root parasiteOrobanche within the xylem of the host tissue were investigated by light- and electronmicroscopy. Coming into contact with the tracheary elements of the host these cells show an unusual differentiation before turning into a water conducting xylem element. From haustorial cells with thickened front walls they develop into typical transfer cells, bearing wall ingrowth in those parts of the wall orientated towards the tracheary elements of the host. During further differentiation the transfer cell changes into a water conducting element by developing the typical secondary wall thickenings of xylem elements within the cell. Partly these wall thickenings are formed inside the labyrinth structures of the transfer cell, always situated opposite those of the tracheary element of the host. Simultaneously the labyrinth disintegrates—some small remnants of wall ingrowths may persist. The protoplast degenerates, and finally a haustorial water conducting element results. Host- und parasitic tracheary elements are connected by pits.

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Wir danken FrauChristl Glockmann für ihre stets verantwortungsvolle Mitarbeit. Den GÄrtnern des Botanischen Gartens in Kiel sei Dank für die oft schwierige Anzucht des Pflanzenmaterials. Die Untersuchungen wurden durch Mittel der Deutschen Forschungsgemeinschaft gefördert.