Evidence for nonclassical alpha adrenoceptor blockade by prazosin in isolated rabbit blood vessels

In isolated rabbit ear artery, prazosin shifted the concentration-response curve for norepinephrine (NE) to the right and increased the slope of the curve in the ED₅₀ region. Prazosin caused a smaller shift to the right of the concentration-response curve for NE in rabbit small saphenous vein and had no effect on the slope in the ED₅₀ region. The prazosin-induced increase in the slope of the NE concentration-response curve did not occur in the ear artery when neuronal and extraneuronal uptake were inhibited by desipramine (DMI) and deoxycorticosterone acetate (DOCA). Prazosin concentration ratios were significantly larger in the ear artery than in the small saphenous vein at all prazosin concentrations in the presence or absence of DMI and DOCA. Significant differences were found between prazosin dissociation constants (K_B) determined at three concentrations of prazosin in ear artery. No such differences were found between phentolamine dissociation constants determined in this vessel. Prazosin dissociation constants determined in small saphenous vein were higher than those determined in ear artery. These findings suggest that prazosin behaves as a noncompetitive antagonist in ear artery and that there are differences between the alpha adrenoceptors of the ear artery and those of the small saphenous vein.     

Three hydroxylations incorporating molecular oxygen in the aerobic biosynthesis of ubiquinone in Escherichia coli.

The biosynthetic origin of the oxygen atoms of ubiquinone 8 from aerobically grown Escherichia coli was studied by 18O labeling. An apparatus was developed which allowed the growth of cells under a defined atmosphere. Mass spectral analysis of ubiquinone 8 from cells grown under highly enriched 18O2 showed that three oxygen atoms of the quinone are derived from molecular oxygen. It was established that the molecular oxygen is incorporated into the two methoxyl groups (at C-5 and C-6) and one of the carbonyl positions of the ubiquinone molecule by demonstrating that only one of the incorporated oxygens will exchange with water under acidic conditions that specifically catalyze the exchange of carbonyl, but not methoxyl, oxygens. That the C-4 carbonyl oxygen is derived from molecular oxygen was shown by the incorporation of three atoms of 18O2 into ubiquinone 8 biosynthesized from added 4-hydroxybenzoic acid. Comparison of ubiquinone 8 and menaquinone 8 from E. coli grown under 18O2 confirmed that the labeled carbonyl oxygen of the [18O2]ubiquinone 8 is incorporated biosynthetically and not by chemical exchange in the cell. It is concluded that the three hydroxylation reactions involved in the pathway for the aerobic biosynthesis of ubiquinone are all catalyzed by monooxygenases. The implications of this study for the anaerobic biosynthesis of ubiquinone 8 in E coli are discussed.     

The partial replacement of the serum growth factor requirement of SV3T3 cells by lactalbumin hydrolyzate.

Lactalbumin hydrolyzate (LH), a commercially prepared, enzymatic digest of a milk protein fraction, can partially replace the serum requirement of SV3T3 cells. In a low, but obligatory, background of calf serum (0.15% v/v), LH carses a large increase in the final cell density (5-10 x over the control) while modestly steimulating the actual growth rate. Lactalbumin hydrolyzate does not contain survival activity for SV3T3 cells and does not affect the growth of 3T3 cells. Since even prolonged exposure to pH 4 or 2 results in complete abolishment of the growth-rate stimulatory capability without affecting the capacity to increase the final cell density, it is possible that the LH growth activity may consist of two dissociable components. All of LH growth activity is water soluble, autoclavable, and resists proteolytic treatment. On Sephadex G15 growth activity appears as a single peak at the void volume but on G25 it is retained beyond the void volume as a broad, skewed peak. The relevant molecular weight range lies between 1,500 and 4,000. The putative low pH resistant material is strongly adsorbed to Dowex 1 x 2 and can be displaced from the column by a reduction in the pH. A comparison of the properties of the LH factors with those of known growth promoting agents isolated from serum and various enzymatic digests indicates that these new factors do not correspond to any of these agents.     

Degradation of feather keratin by culture filtrates of Streptomyces fradiae.

Treatment of milled defatted capon feathers with filtrates of Steptomyces fradiae ATCC 10745 that had been concentrated 20 times showed that the most keratin degradation in 0.5h occurred at pH 8.0 and 60degrees C. If assay time was extended, however, adecrease in reaction rate occurred and appeared to result from keratinase instability at elevated temperatures. Exposure of commercial feather meal to unconcentrated culturefiltrates for 15 h produced greatest degradation at 50 degrees C.     

Seasonal and diurnal changes in the water temperature of a temperate pond (England) and a tropical pond (Kenya)

Seasonal changes in water temperatures, embracing periods of low, rising, high and declining temperatures, were recorded in both a temperate and a tropical pond. In the course of a year, the range between the lowest and highest average weekly temperatures was greater in the temperate pond. The spans between the average minimum and the average maximum weekly water temperatures in the warmest months of the year in the tropical pond were greater than those found at any time of the year in the temperate pond. The average weekly air and water temperatures showed the same pattern of seasonal fluctuations; in the tropical pond the average weekly air temperatures were always less than the average minimum weekly water temperatures, whereas they were below, within or above the spans between the average minimum and average maximum weekly aquatic temperatures, according to the time of year, in the temperate pond.In both ponds, diurnal fluctuations were absent during the cooler months; the amplitudes of the fluctuations in the warmer months varied according to the time of year, and were greater, during the warmest months, in the tropical pond. In both ponds lowest temperatures were recorded sometime between 0200 and 1000 hours and highest between 1200 and 2000 hours.The influence of temperature on the life-cycles of invertebrates in both ponds is discussed briefly.

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Zusammenfassung Jahreszeitlich bedingte Schwankungen in der Wassertemperatur, welche Perioden mit niedriger, ansteigender, hoher und abfallender Temperatur einschlossen, wurden in einem gemäßigten und in einem tropischen Teich festgestellt. Im Laufe eines Jahres war der Unterschied zwischen den tiefsten und höchsten wöchentlichen Durchschnittstemperaturen im gemäßigten Teich größer. Hingegen war der Abstand zwischen Mindest- and Höchsttemperatur des Wassers im Wochendurchschnitt während der warmsten Monate des Jahres im tropischen Teich größer als zu irgendeiner Jahreszeit im gemäßigten Teich. Der Wochendurchschnitt der Luft- und Wassertemperaturen wies das gleiche jahreszeitlich bedingte Schwankungsmuster auf. In dem tropischen Teich war die wöchentliche Durchschnittstemperatur der Luft stets niedriger als die Mindestdurchschnittstemperatur des Wassers in einer Woche. Jedoch lag sie — je nach Jahreszeit — unterhalb, auf gleicher Höhe oder oberhalb der Spannweite der niedrigsten and der höchsten wöchentlichen Dutchschnittstemperaturen des Wassers im gemäßigten Teich.In beiden Teichen traten die taglichen Schwankungen während der kÜhleren Monate nicht auf. Der Umfang der Schwankungen in den wärmeren Monaten variierte je nach Jahreszeit and war in den wärmsten Monaten in dem tropischen Teich größer. In beiden Teichen wurden die tiefsten Temperaturen zwischen 2.00 and 10.00 Uhr and die höchsten zwischen 12.00 and 20.00 Uhr gemessen.

     

Proton magnetic relaxation studies of the interaction of D-xylose and xylitol with D-xylose isomerase. Characterization of metal-enzyme-substrate interactions.

The interaction of D-xylose isomerase purified from two sources with Mn2+ and D-xylose or the competitive inhibitor xylitol has been examined by nuclear magnetic resonance. A greater paramagnetic effect of enzyme-bound Mn2+ on the alpha anomer of D-xylose than on the beta anomer was observed, providing independent evidence for the specificity of D-xylose isomerase for the alpha anomeric form of D-xylose. The exchange rate of alpha-D-xylose into the ternary complex, determined from the normalized paramagnetic contribution to the transverse relaxation rate (1/fT2p) of the carbon 1 proton of alpha-D-xylose, exceeds Vmax for the enzymatic reaction by 3 orders of magnitude. The amount of xylitol necessary to displace alpha-D-xylose from the substrate-enzyme-Mn2+ complex is consistent with the Km value for alpha-D-xylose and the inhibitor constant Ki for xylitol previously determined by the methods of enzyme kinetics. These results suggest that the NMR experiments observe complexes of D-xylose isomerase which are kinetically and thermodynamically competent to participate in catalysis. From the frequency dependence of the paramagnetic contribution to the longitudinal relaxation rate (1/T1p) of the carbon 1 proton of alpha-D-xylose, the correlation time (tauc) which modulates the dipolar interaction between enzyme-bound Mn2+ and alpha-D-xylose has been determined (5.1 x 1o(-10) s). From these observations a range of calculated distances between enzyme-bound Mn2+ and the carbon 1 proton of alpha-D-xylose (9.1 +/- 0.7 A) has been found. The enzyme-bound Mn2+ has comparable effects on the carbon 1, carbon 2, and carbon 5 protons of alpha-D-xylose, suggesting that these protons of the enzyme-bound substrate are equidistant from the bound Mn2+. A similar distance (9.4 +/- 0.7 A) between the enzyme-bound Mn2+ and the terminal methylene protons of xylitol, an analog of the open chain intermediate in the reaction, has been determined. The results of the present substrate relaxation and previous water relaxation studies suggest that two small ligands such as water molecules or a large portion of the protein intervene between the bound metal ion and the bound substrate in the active ternary complex.