Regeneration of NADH with immobilized systems of alanine dehydrogenase and hydrogen dehydrogenase

Summary An alternative approach to the regeneration of coenzymes using immobilized hydrogen dehydrogenase (hydrogenase) is described. Hydrogenase isolated from Alcaligenes Eutrophus was immobilized to porous glass particles and used in combination with alanine dehydrogenase for formation of alanine, while the NADH consumed was regenerated by molecular hydrogen. Different physical arrangements of the two enzymes were compared. Alanine was conveniently assayed with a specially designed enzyme thermistor method.     

Involvement of smooth and coated vesicles in the function of the contractile vacuole complex of some cryptophycean flagellates

The contractile vacuole complex of cryptophycean flagellates comprises the contractile vacuole, a pore and a vesicular spongiome. A minority of spongiome vesicles bear a 15-nm coat on the cytoplasmic surface of the membrane. The coat superficially resembles a clathrin coat. The majority of vesicles are smooth surfaced. Both types of vesicles are found at the same time. Smooth vesicles can be seen in profile suggesting vesicle-vesicle and vesicle-vacuole fusion. It is suggested that smooth vesicles are involved in the segregation of fluid from the cytoplasm and in filling the vacuole. Coated elements exist only as independent vesicles and as coated pits in the contractile vacuole membrane. There is no evidence of fusion of coated vesicles. It is suggested that coated vesicles function to retrieve specific membrane components from the contractile vacuole.     

Versuche zum angenommenen Kontrastverlust im Gesang der Blaumeise (Parus caeruleus) auf Teneriffa

Zusammenfassung Der Gesang von Blaumeisen-Populationen in Mitteleuropa, Spanien, Marokko und auf Teneriffa wurde miteinander verglichen (Abb. 1). In Süddeutschland und auf Teneriffa wurden Klang-Attrappen-Versuche durchgeführt.1. Der Blaumeisen-Gesang ist in Marokko und auf Teneriffa sehr ähnlich. Er unterscheidet sich vom Blaumeisengesang in Europa (Mitteleuropa und Spanien) in folgenden Eigenschaften (2.–4.):2. Ihm fehlen phrasierte Strophen (Abb. 2 a–c, e, 3, 4 a, b, f, g), also Strophen, in denen dasselbe Element mindestens viermal nacheinander wiederholt wird.3. Er enthält mehr verschiedene Elemente (Abb. 5, 7).4. Die interindividuelle Variation ist größer (Abb. 6, 7).5. Die Unterschiede zwischen dem Blaumeisen-Gesang in Europa und auf Teneriffa lassen sich nicht mit der Kontrast-Betonungs- und der Kontrast-Verlust-Hypothese nachLack &Southern (1949) undMarler (1960) erklären. Die Lernentzugs-Hypothese erklärt sie besser.6. Die Blaumeisen von Teneriffa und Marokko sind sehr nahe miteinander verwandt, aber vermutlich sind sie von den europäischen Blaumeisen artlich nicht getrennt.

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The song of the Blue Tit (Parus caeruleus) on Tenerife: Experiments on a presumed loss of contrast

Summary Songs of Blue Tit populations from Central Europe, Spain, Morocco and Tenerife (fig. 1) were compared. Playback experiments were made in South Germany and on Tenerife.1. Blue Tit songs from Morocco and Tenerife are very similar. They differ from songs of Blue Tits in Europe (Central Europe and Spain) in the following characteristics (2–4):2. Lack of phrased songs (fig. 2 a–c, e, 3, 4 a, b, f, g), i. e. songs with the same notes repeated successively at least four times.3. A greater number of different types of notes (fig. 5, 7).4. Greater interindividual variation (fig. 6, 7).5. Differences between Blue Tit song from Europe and from Tenerife cannot be explained by the hypothesis of contrast reinforcement and loss of contrast, according toLack &Southern (1949) andMarler (1960). The withdrawal of learning hypothesis is a better explanation.6. Blue Tits on Tenerife and Morocco are very closely related to each other but are probably not a different species from the Blue Tits of Europe.

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Für die Übersetzung danken wir FrauR. Jellis und HerrnP. Lundberg.     

The effect of sodium chloride on the structure of ribonucleoprotein particles from rat liver nuclei.

38S (monoparticles) and greater than 50--200S ribonucleoprotein particles (polyparticles) from rat liver nuclei were treated with increasing concentrations of sodium chloride. Treatment of 38S or greater than 50--200S particles, with 0.14, 0.25, 0.5, 1.0, and 2.0M NaCl resulted in a decrease of protein to RNA ratios from 8 to 3.1 for 38S particles and from 4.0 to 1.5 for greater than 20--200S particles. Correspondingly the densities in CsCl increased. Whereas the maximum of the sedimentation profile of polyparticles decreased from 90S to 50S after treatment with increasing NaCl concentrations, a discontinuous change was found in the case of monoparticles. It was shown by sodium dodecyl sulfate-polyacrylamide gel electrophoresis that the proteins which were dissociated by NaCl were in the molecular weight range of 30--45 000. Four of the 5 small molecular weight RNAs in the range of 4.5 to 8S remained tightly associated even after treatment of polyparticles with 2.0M NaCl. When 38S or 70--200S nRNP particles were exposed to increasing concentrations of NaCl (0.25, 0.5, 1.0, 2.0M), the molar ellipticity at 264 nm increased progressively to about 40%. Upon NaCl treatment of polyparticles and successive removal of the dissociated proteins by centrifugation the increase in the positive CD band at 264 nm was only 15%.     

Identification and quantitative determination of the flavin component of soluble hydrogenase from Alcaligeneseutrophus

The flavin component of soluble hydrogenase (hydrogen: NAD⁺ oxidoreductase, EC 1.12.1.2) from $\text{Alcaligenes}\text{eutrophus}$ was identified as FMN by thin layer chromatography in two solvent systems and by binding studies with apoflavodoxin from $\text{Megasphaera}\text{elsdenii}$. The flavin of hydrogenase reacted rapidly with apoflavodoxin with almost complete quenching of the fluorescence at 525 nm. Quantitative determination of FMN was performed by fluorimetric titration with a standardized solution of apoflavodoxin. From the determined FMN content of different enzyme preparations and from the percentage of stimulation of hydrogenase activity by exogenous FMN it is concluded that hydrogenase contains 2 FMN per molecule.