Mapping of repetitive bovine DNA sequences on cattle Y chromosomes.

Three male-specific PCR products of the sequences BC1.2, lambda ES6.0, and BRY.1 were used as probes for Southern blot analyses. Each of these probes generated a complex male-specific band pattern, which showed some quantitative variations among bulls. Hybridization patterns obtained with the BC1.2 and lambda ES6.0 PCR products were interrelated. Chromosomal locations of these repeats were determined by hybridizing the tritiated PCR products in situ to male metaphase spreads. The BC1.2 and lambda ES6.0 PCR products hybridized to Yp13-->p12, whereas the BRY.1 PCR product hybridized over the entire Y chromosome. In addition, the BC1.2 and lambda ES6.0 PCR products hybridized to the distal half of the acrocentric Y chromosome of Bos indicus, indicating that the short arm of the B. taurus Y chromosome is homologous with the telomeric end of the B. indicus Y and supporting the notion that the Y chromosomes of these two species differ by a pericentric inversion.     

A new method for measuring tree height in tropical rain forest

Abstract. A new method is described for measuring tree height in tropical forest with a dense undergrowth, the so-called angles-measure method, which is related to the height-matching method formerly used by British foresters.     

A suitable method to monitor inhibition of cholinesterase activities in tissues as induced by reversible enzyme inhibitors

A radiometric method has been used to estimate in vivo activities of cholinesterases in various tissues in the presence of reversible inhibitors. Determination of the samples was performed with the lowest possible degree of dilution to avoid reactivation of the enzyme which would prevent reliable calculation. Dose-response curves and concentration-response curves were performed using physostigmine and tetrahydroacridine, two reversible anticholinesterases in clinical use. Specific inhibition of acetyl- and butyrylcholinesterase was performed using BW284C51 and iso-OMPA, respectively.     

Effect of intake on digestibility of plant cell walls and cell contents of complete diets for ruminants

Three diets, designated HH, H and L, containing 24.6, 32.7 and 41.5% cell walls (CW), respectively, were given to sheep at submaintenance and maintenance levels, and to milking cows ad libitum (more than three times the energy requirement for maintenance). Increased daily intake, as a multiple of maintenance requirements, decreased digestible organic matter (DOM) by 4.9, 6.0 and 3.8 units for diets HH, H and L, respectively. Approximately 70% of this decrease could be accounted for by a decrease in the digestibility of the cell walls fraction. It is emphasized that the other 30% is not entirely due to depression in DOM of the cell contents. It includes an element of endogenous faecal material, and there are references to indicate it increases with level of feeding.     

A transglycosylating 1,3(4)-beta-glucanase from rhodothermus marinus NMR analysis of enzyme reactions.

The enzymatic hydrolysis of polysaccharides by the 1, 3(4)-beta-glucanase (LamR) from Rhodothermus marinus has been explored. The enzyme cleaves the 1,3-beta-linkages of 3-O-substituted glucose units in 1,3-beta-glucans such as laminarin and curdlan, and also the 1,4-beta-linkages of 3-O-substituted beta-glucose in beta-glucans such as lichenin and 1,3-1, 4-beta-glucan from the cell walls of barley endosperm. The polysaccharide substrates (laminarin, curdlan and barley beta-glucan) were characterised using NMR spectroscopy. The reaction of LamR with its substrates was followed by recording one-dimensional and two-dimensional 1H-NMR and 13C-NMR spectra at suitable time intervals after addition of the enzyme. It is shown that hydrolysis occurs with retention of the anomeric configuration and that LamR performs transglycosylation to generate both 1, 3-beta-glycosidic and 1,4-beta glycosidic linkages. The transglycosylation results in, e.g. formation of the trisaccharide 4-O-glucosyl-laminaribiose from exclusively 1,3-beta-oligoglucosides. When barley 1,3-1,4-beta-glucan was incubated with LamR the beta-1, 4-linkages of 3-O-substituted beta-glycosyl residues were rapidly hydrolysed. Simultaneously de novo formation of 1,3-beta-glycosidic linkages was observed which, however, were cleaved during prolonged incubations. It is shown that a laminaribiosyl unit is the minimum requirement for formation of an enzyme-substrate complex and subsequent hydrolysis/transglycosylation.     

Infiltration phyto- and protozooplankton assemblages in the annual sea ice of Disko Island, West Greenland, spring 1996

During the spring of 1996 we occupied a station on annual sea ice located several kilometers from Disko Island, West Greenland in water depths greater than 200 m. The goal of this 3-week field season was to characterize sea-ice communities and the underlying water column prior to, and during, ice break-up. A heavier than usual snow load depressed the sea ice below sea level and the snow-ice interface became flooded. Some of this flooded region subsequently refroze and the whole process repeated itself when additional snow accumulated. The infiltration phytoplankton and protozooplankton assemblages that developed in this region were abundant and diverse. Algal biomass in the infiltration layer was approximately an order of magnitude greater than in the underlying water column but an order of magnitude less than in the well-developed bottom ice community. The infiltration autotrophic assemblage resembled the bottom-ice assemblage while the protozooplankton assemblage was more similar to the water column assemblage. Received: 13 February 1998 / Accepted: 30 May 1998     

Comparison of insulin antibody levels during the first 3 years of treatment of adult diabetics with monocomponent porcine lente-insulin and single peak beef NPH insulin

Insulin antibody production was studied in two groups of 9 adult diabetics each, who were never treated before with insulin. One group received Monocomponent porcine lente insulin (MC) and the other group single peak beef NPH insulin, for 3 years. Insulin antibodies were evaluated by antibody-bound immunoreactive insulin (Abl) and by the labelled insulin binding capacity (IBC) which presented a significant correlation best fitted by a logarithmic curve. The patients treated with MC insulin developed significant levels of insulin antibodies, however, at lower levels and appearing later in comparison to those with beef NPH. Only 3 patients did not produce significant levels of insulin antibodies. The highest titers occurred after different lengths of treatment in the two groups of patients. Abl decreased after continuation of treatment particularly in the MC series. While in the MC-treated patients there was some positive correlation between the insulin dose and the level of Abl no significant correlation was found between the diabetes control and insulin antibody titers in both groups of patients.