Cytochrome c peroxidase compound I: formation of covalent protein crosslinks during the endogenous reduction of the active site

Cytochrome c peroxidase (ferrocytochrome-c:hydrogen-peroxide oxidoreductase, EC 1.11.1.5) was oxidized by hydrogen peroxide in the absence of exogenous electron donor. Higher molecular weight species were observed in the decay products at pH 4.5. Monomer and dimer were separated by gel filtration and purified by anion-exchange chromatography. Peptide mapping of tryptic digests of the dimer indicated a tyrosine crosslink localized between residues 32 and 48 of the native enzyme.     

A note on the Olduvai clavicular fragment

Certain features of the Olduvai clavicular fragment have been examined in the light of data already existing on the form of the clavicle in primates. Although similar to that of modern man, the fragment exhibits features which suggest that its function may have differed somewhat from that of the clavicle in man. The new information correlates well with that obtained from the fragmentary Sterkfontein scapula.     

Report of the Council of the Association of Applied Biologists for the year 1968

Bock (1963) showed that in the years 1956-60 early season sprays achieved good control of coffee berry disease (CBD) in East Rift areas of Kenya. In recent years, however, this spray programme has given erratic and often very poor results. In field experiments in 1966 yields of main (late) crop were increased from 151 to 652 kg/ha by early season sprays but in 1967 practically no control of the disease was achieved. Of the fungicides examined captafol was superior to copper; ‘Tuzet’, the best antisporulant, gave the poorest control. Analysis of the data indicates that this large seasonal variation depends on the very different inter-relationships between rainfall, cropping pattern and timing of sprays which obtained in the 2 years. The hypothesis that early-season sprays achieve control of CBD mainly by reducing the sporulating capacity of the maturing bark is questioned. The view is put forward that the protectant action of these sprays has been underestimated.     

Differential induction of activation markers in macrophage cell lines by interferon-gamma

Macrophage cell lines were used in these studies as a model system to dissect the biochemical and functional mosaic of the macrophage activation process. In particular, the requirements for the induction of tumoricidal and bactericidal activity in the RAW 264.7 and WEHI-3 cell lines by interferon-gamma (IFN-gamma) and bacterial lipopolysaccharide (LPS) were determined. Changes in expression of a series of macrophage markers traditionally associated with macrophage activation were monitored during stimulation of the cells in order to determine whether a detectable pattern of activation-associated changes is associated with the development of a particular functional activity. These markers included changes in the cell surface expression of major histocompatibility complex-encoded Class I and Class II antigens and antigens in the Mac-1/LFA-1 family, alterations in the levels of membrane enzymes (5' nucleotidase and alkaline phosphodiesterase), and production of secretory products including hydrogen peroxide and the monokines interleukin-1, interferons-alpha/beta, and tumor necrosis factor-alpha. Our results demonstrate that a given homogeneous macrophage population expresses a distinct subset of functional activities in response to single, defined activating signals such as IFN-gamma and LPS. The display of a variety of macrophage surface antigens, enzymes, and secreted products is activated simultaneously by such treatment; however, the particular pattern of such activation-associated markers cannot reproducibly be used to predict the ability of an activated cell to perform a particular function. The results also suggest that macrophage cell lines expressing differential response patterns following IFN-gamma stimulation provide a valuable system for dissection of the molecular and cell biology of macrophage activation.     

The diagnosis of antileptospiral antibodies in human subjects by solid-phase immunoenzyme analysis

The possibility of using the enzyme-linked immunosorbent assay (ELISA) for the diagnosis of leptospirosis has been shown. This method has proved to be more simple and sensitive than the leptospiral microagglutination and lysis test. The data on obtaining genus-specific leptospiral antigens are presented. As revealed in this study, the antigens obtained by the complex treatment of microbial cells with ultrasound and detergents show the maximum activity in ELISA. The optimum parameters of the ELISA system for the diagnosis of leptospirosis have been established.