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The O-K-spectra of α- and γ-Al2O3, β-Ga2O3 and In2O3 were measured with a high-resolution grating spectrograph using the method of electron excitation. The spectra were corrected for the nonlinear response of the photographic emulsions. A shift of the O - K-emission band edge of γ-Al2O3 to lower energy with respect to that of α-Al2O3 and a fine structure within all O -K-bands were observed for the first time. The details of the spectra are discussed in relation to the energy level diagrams, crystal structure, and chemical bond of these oxides.
Differential derepression of the genome of potato tuber cells causes the onset of a vigorous metabolic activity, which is initiated by rapid synthesis of different RNA species, various proteins and phospholipids. Consequently enhanced respiration and the build up of cell compartments such as ribosomes and mitochondria as well as the performance of cell divisions and suberization of new-formed cell walls occur. Although there is an activation of metabolism in general with a concomitant rise in concentration of most glycolytic metabolites — as was proved for fructose-1.6-diphosphate, dihydroxyacetone, glyceraldehade-3-phosphate, phosphoenolepyruvate and pyruvate — the activities of the corresponding enzymes do not reflect these uniform metabolic changes. Aldolase and in a pronounced manner enolase and glutamate — pyruvate — transaminase lower their activities suddenly after derepression. The activity of triosephosphateisomerase remains constant. In contrast phosphoglyceromutase, pyruvate kinase and to a lower extent malic enzyme enhance their action during the same time.
Without doubt, differential lowering and enhancing the activity of glycolytic chain constituents at the same time is an important regulatory mechanism of the cell. The activation represents de novo synthesis of the protein concerned whereas the inactivation depends largely on protein synthesis. This is clearly shown by experiments with inhibitors of protein synthesis.
It is proposed that this differential synthesis and degradation represent a “long-time-regulation” of enzymatic activity of the cell in contrast to the known “short-time-regulation” by feedback or competition.
Es werden allgemeine Gleichungen zur Berechnung der Verteilung der Nullstellen von der großen kanonischen Verteilungsfunktion Ξ (y) eines Gittergases in der komplexen Ebene der Fugazität y in Bethescher Näherung angegeben, die nach einem graphischen Verfahren gelöst werden können. Für das zweidimensionale, quadratische Gitter und das dreidimensionale, kubische Gitter werden die Bestimmungsgleichungen für die Nullstellenverteilung mit Hilfe des graphischen Verfahrens explizit gelöst. Die Nullstellenverteilung von Ξ (y) des eindimensionalen Gittergases wird in geschlossener Form angegeben.
Hellmuth Rößler [: Nekrolog]
(1969)
Fluorescense spectra of lactate dehydrogenase * (E.C. 1.1.1.27) were investigated in the presence of the coenzyme fragments dihydronicotinamide mononucleotide and dihydronicotinamide-ribose-5'-pyrophospho- (P2) -5“-ribose. The reduced mononucleotide is enzymatically less active as a hydrogen donor. However, formation of a complex with the enzyme was not observed under the conditions used. All the other substances: dihydronicotinamide-ribose-5'-pyrophospho- (P2) -5“-ribose, dihydronicotinamide- benzimidazole-dinucleotide, dihydronicotinamide-3-desazapurine-dinucleotide and dihydronicotinamide-6-mercaptopurine-dinucleotide form more or less stable complexes with lactate dehydrogenase. The complexes do not markedly differ from the complex formed with the natural cofactor. In all cases spectra indicate change in conformation of the coenzyme by forming the coenzyme-enzyme-complex which has been proposed by VELICK 1 too. The cysteine residues of the lactate dehydrogenase are not essential for binding the coenzyme to the active center; this was shown with mercury blocked enzyme.
Excimerenfluoreszenz oligomerer Assoziate von 3,4-Benzpyren in wäßrigen Lauryl-Sulfonat-Lösungen
(1969)
An Lösungen von 3,4-Benzpyren in wäßrigen Na-Laurylsulfonatlösungen wird etwa bei der doppelten kritischen Konzentration der Mizellbildung eine langwellige Fluoreszenz beobachtet, deren spektrale Zusammensetzung innerhalb der Toleranz der spektralen Zusammensetzung der Fluoreszenz des festen Kohlenwasserstoffs gleicht.
Wegen der eigenartigen Konzentrationsabhängigkeit wird diese Emission Excimeren zugeschrieben, die sich - in Analogie zum Excimeren-Mechanismus der Festkörperfluoreszenz von 3,4-Benz pyren - aus im Grundzustand vorliegenden Assoziaten bilden, die nach der Excimeren-Emission wieder zurückgebildet werden.
In der Monte Cavallo-Gruppe fand Verf. in Stauseesedimenten fossile Holzstücke, für die die 14 C-Datierung ein Alter von 29 350 ± 460 Jahren vor 1950 n. Chr. ergab. Die schluffigen Ablagerungen, die in etwa 900 m, fast 80 m über dem heutigen Flußbett des T. Caltea aufgeschlossen sind, ruhen auf Schottern und werden von Moräne überlagert.
Aufgrund seiner stratigraphischen Lage und seines 14C-datierten Alters kann das Holz (Picea abies bzw. Larix) einem zeitlichen Äquivalent des Paudorf-Interstadials zugeordnet werden. Dieser Fund von Großresten ermöglicht somit eine erste absolute Datierung des Paudorf-Interstadials für die Südalpen und Oberitalien.