ABSTRACT
High levels of nitrogen fixation have been observed in the wastewaters of pulp and paper mills. In this study, we show that nitrogen fixation in a model pulp and paper wastewater treatment system is supported by a high density of nifH sequences that are of low diversity. Quantitative PCR revealed a ratio of nifH to 16S rDNA of 1.14 +/- 0.76 which shows that very high levels of the nifH gene were enriched to support the high rates of nitrogen fixation that occur in this wastewater. Changes in wastewater composition and dissolved oxygen levels did not affect the nifH levels and allowed stable wastewater treatment. The nifH sequences identified display a similar profile to those seen in forest soil environments where nifH sequences derived from alpha-proteobacteria and beta-proteobacteria are also prevalent.
Subject(s)
Bacteria/enzymology , Bacterial Proteins/genetics , Industrial Waste/analysis , Nitrogen Fixation , Oxidoreductases/genetics , Water Microbiology , Bacteria/classification , Bacteria/genetics , Bacteria/isolation & purification , Bacterial Proteins/metabolism , Biodiversity , DNA, Bacterial/genetics , DNA, Ribosomal/metabolism , Molecular Sequence Data , Oxidoreductases/metabolism , Phylogeny , RNA, Ribosomal, 16S/geneticsABSTRACT
The classical methods for estimating the volume of human body compartments in vivo (e.g. skin-fold thickness for fat, radioisotope counting for different compartments, etc.) are generally indirect and rely on essentially empirical relationships--hence they are biased to unknown degrees. The advent of modern non-invasive scanning techniques, such as X-ray computed tomography (CT) and magnetic resonance imaging (MRI) is now widening the scope of volume quantification, especially in combination with stereological methods. Apart from its superior soft tissue contrast, MRI enjoys the distinct advantage of not using ionizing radiations. By a proper landmarking and control of the scanner couch, an adult male volunteer was scanned exhaustively into parallel systematic MR 'sections'. Four compartments were defined, namely bone, muscle, organs and fat (which included the skin), and their corresponding volumes were easily and efficiently estimated by the Cavalieri method: the total section area of a compartment times the section interval estimates the volume of the compartment without bias. Formulae and nomograms are given to predict the errors and to optimize the design. To estimate an individual's muscle volume with a 5% coefficient of error, 10 sections and less than 10 min point counting (to estimate the relevant section areas) are required. Bone and fat require about twice as much work. To estimate the mean muscle volume of a population with the same error contribution, from a random sample of six subjects, the workload per subject can be divided by square root of 6, namely 4 min per subject. For a given number of sections planimetry would be as accurate but far more time consuming than point counting.
Subject(s)
Body Composition , Magnetic Resonance Imaging/methods , Humans , Male , Mathematics , Middle Aged , Reference ValuesABSTRACT
Mössbauer spectroscopic studies of whole cells of Pseudomonas aeruginosa, grown under different conditions, indicate that the predominant form of iron in the cells varies significantly. These differences are interpreted in terms of differences in the nature of the iron cores of the bacterial ferritin, which result from different growth conditions.
Subject(s)
Ferritins/metabolism , Iron/metabolism , Pseudomonas aeruginosa/metabolism , Anaerobiosis , Pseudomonas aeruginosa/growth & development , Spectroscopy, Mossbauer/methodsABSTRACT
Haemosiderin isolated from different iron-loading syndromes, primary haemochromatosis (PHC) and secondary haemochromatosis (SHC) biochemically exhibited differences in both their iron core and peptide composition. The rate of release of iron from PHC haemosiderin to oxalate was 3-fold greater than that from SHC haemosiderin. The major peptides separated by SDS-PAGE showed a major band at Mr 20,000 for PHC haemosiderin and at Mr 15,000 for SHC haemosiderin.
Subject(s)
Hemochromatosis/metabolism , Hemosiderin/isolation & purification , Iron/analysis , Liver/analysis , Spleen/analysis , Deferoxamine , Ferritins/isolation & purification , Hemochromatosis/etiology , Humans , Molecular WeightABSTRACT
Mössbauer spectroscopy has indicated significant differences in the iron-containing cores of various haemosiderins. In the present study, haemosiderin was isolated from a number of animal species including man. In addition, haemosiderin was isolated from patients with primary idiopathic haemochromatosis or with secondary (transfusional) iron-overload. The iron cores of the animal and normal human haemosiderin appear to be very similar by Mössbauer spectroscopy, and the electron diffraction data indicate a ferrihydrite structure similar to that of ferritin cores. The haemosiderin isolated from secondary iron-overload shows anomalous behaviour in its temperature-dependent Mössbauer spectra. This can be understood in terms of the microcrystalline goethite structure of the cores as indicated by electron diffraction. The haemosiderin cores obtained in the case of primary haemochromatosis have an amorphous Fe(III) oxide structure and show Mössbauer spectra characteristic of a magnetically disordered material, which only orders at very low temperatures.
Subject(s)
Hemochromatosis/blood , Hemosiderin , Animals , Electrons , Humans , Microscopy, Electron , Scattering, Radiation , Spectroscopy, Mossbauer , TemperatureABSTRACT
Haemosiderin iron cores isolated from patients with secondary haemochromatosis have a goethite-like (alpha-FeOOH) crystal structure whereas those from patients with primary haemochromatosis are amorphous Fe (III) oxide. Haemosiderin cores isolated from normal human spleen are crystalline ferrihydrite (5Fe2O3.9H2O). The disease-specific structures are significantly different from the ferrihydrite structure of associated ferritin cores. The results are important in understanding the biological processing of iron in pathological states and in the clinical treatment of iron-overload diseases.
Subject(s)
Hemochromatosis/metabolism , Hemosiderin , Iron , Crystallization , Dialysis , Electrophoresis, Polyacrylamide Gel , Ferric Compounds , Ferritins/analysis , Hemosiderin/analysis , Humans , Iron/analysis , Iron/metabolism , Liver/analysis , Microscopy, Electron , Oxalates , Oxalic Acid , Proteins/analysis , Solubility , Spectrometry, Gamma , Spleen/analysisABSTRACT
A new technique is reported resulting in the direct, instantaneous analyses of trace compounds in breath. The analyses were performed using a commercial atmospheric pressure chemical ionization mass spectrometer (TAGA TM2000 APCI mass spectrometer). A known flow of breath sample is introduced into the ionization region of the mass spectrometer. The study includes the measurement and monitoring in real-time, of breath ammonia during a 24 hour and a 48 hour period. The ammonia profiles indicate a personalized daily pattern associated with each subject. This method appears to be of potential value in routine detection and treatment of hyperammonemia patients. Results also show that it is possible to obtain instantaneous analyses of several naturally occurring metabolites and other substances on breath in the ppm to ppt range, suggesting a number of diagnostic research applications.