The pH-conditional, ammonia assimilation-deficient mutants of Hydrogenomonas eutropha - Isolation and growth characteristics
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A crossed-beam apparatus is used to measure the product ion velocity and angular distributions for the following ion-molecule reactions in the relative energy range from 2 to 9 eV: CH4(+) + NH3 yields NH4(+) + CH3; CH4(+) + NH3 yields CNH5(+) + H2; NH2(+) + CH4 yields CNH4(+) + H2 (or 2H); and CH3(+) + NH3 yields CNH4(+) + H2 (or 2H). These reactions are also studied by means of deuterium labeling as a further probe of the detailed reaction dynamics. Probability contour plots for the four reactions are constructed in Cartesian velocity space, and product peaks in the plots are discussed. Relative cross sections and Q values are computed for two of the reactions as well as for the corresponding deuterium-labelled reactions. The results show that the present ion-neutral condensation reactions are highly exothermic with a deep well for the internal complex, that little hydrogen scrambling occurs, and that the energy of the reactions is released mainly as internal energy, even to the extent of producing two hydrogen atoms in some cases rather than one hydrogen atom or molecule.
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The detection of transitions in NH2D at 85926.2 and 110153.4 MHz from the Orion molecular cloud is reported. An 11-m radio telescope with an 80-120 GHz cooled Cassegrain receiver and a tunable quasi-optical rejection filter was used in the investigations. Equations of statistical equilibrium for the lowest 34 energy levels of NH2D were solved. It seems unlikely that the observed lines arise in the very extended CO cloud. However, they could originate either in the molecular 'ridge' or the unresolved (Kleinmann-Low) core of the cloud or both. A column density of about 50 trillion/sq cm is deduced. The NH2D spectra, with 1 MHz resolution, are shown in a graph. Using previously reported column densities for NH3, a value of 0.05 with an estimated maximum uncertainty factor of 10 is found for the ratio NH2D/NH3.
Comparison of infrared solar spectra in the 750 to 950 kayser region obtained during sunrise and sunset shows that a number of features due to the nu-2 NH3 band are present on the sunset spectra but are indicated by only a trace on the sunrise spectra. The sunset path shows approximately 0.007 atm-cm NH3, and the reason for the discrepancy between sunrise and sunset spectra is not known. The ground-based measurements at Denver were obtained with a 0.06 kayser resolution.
A one-dimensional tropospheric photochemical model is used to simulate measured profiles of NH3 obtained with the Infrared Heterodyne Radiometer. The relative roles of homogeneous loss, heterogeneous loss, and vertical eddy transport are discussed in terms of selecting parameters which best fit the measurements. The best fit was obtained for a vertical eddy diffusion coefficient of 200,000/sq cm per sec or greater (corresponding to a characteristic vertical transport time in excess of about 35 days), and a characteristic heterogeneous loss time in excess of 10 days. The characteristic homogeneous chemical loss time was found to be about 40 days at the surface and decreased to about 180 days at 10 km, and not very sensitive to model chemical perturbations. Increased ground-level concentrations of NH3 to about 10 ppb, compared to background surface concentrations of about 1 ppb, were measured several weeks after application of ammonium nitrate fertilizer. This suggests that the volatilization of ammonium nitrate fertilizer is rapid, and an important source of NH3. Because of the characteristic times for the loss mechanisms, synoptic time-scale phenomena may play an important role in determining the tropospheric distribution of NH3 concentrations.
Theoretical rate constants are presented for excitation of NH3 by collisions with He. The lowest 22 levels of ortho-NH3 and the lowest 16 levels of para-NH3 are considered at kinetic temperatures of 15 to 300 K.
The presence of NO2(-) in the external solution increased the overall efficiency of the mixed N sources by cereal leaves. The NH4(+) in the substrate solution decreased the efficiency of NO3(-) reduction, while NO3(-) in the substrate solution increased the efficiency of NH4(+) assimilation.
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