Evaluation of a mobile computerized grain feeder for lactating cows grazing grass pasture

The objective of this study was to evaluate a mobile computerized grain feeder for use to feed individually Holstein cows grazing grass pasture. Thirty-two Holstein cows averaging 95 d of lactation and 39.3 kg/d of milk were rotationally grazed on predominantly Dactylis glomerata pastures for 9 wk starting in early May. Cows were blocked according to parity, days of lactation, and milk yield. Cows were randomly assigned to a control group in which cows were individually fed grain twice daily at milking or to a group that was offered grain four times daily using a mobile grain feeder in the pasture. Cows in both groups were offered 1 kg of grain/3 kg of milk; pasture was the only source of forage. Cows fed using the mobile grain feeder consumed less grain than did control cows (9.3 vs. 11.3 kg/d) and tended to yield less milk, but with a higher fat content. A separate analysis was conducted using data from only those cows that were fed using the mobile grain feeder and that consumed, in four relatively equal amounts, at least 75% of the allotted grain of their respective pairmates (7 per group) in the control group. When cows that were using the mobile grain feeder consumed amounts of grain comparable with that of the controls, more frequent grain feeding did not alter milk yield or composition. Plasma samples (five per cow per treatment) were collected at 2-wk intervals to measure glucose, urea N, and nonesterified fatty acids (NEFA). Plasma glucose and urea N were not affected by treatment and averaged 54.9 and 19.9 mg/ dl for all cows, respectively. Cows fed grain using the mobile feeder had higher (212.4 vs. 170.5 meq/L) concentrations of NEFA than did control cows, but, when cows consumed greater than 75% of their allotted grain from the mobile feeder, concentrations of NEFA were similar. The mobile grain feeder can be used to feed cows individually on pasture; however, adaptation of the cows to the mobile grain feeder appears to be important.     

How much is a collaboration worth? A calibrated bibliometric model

Interest in collaboration is increasing in policy circles. There are numerous international and national programs to encourage collaboration, for example, between university and industry researchers. However, little is know about the way in which collaboration changes the impact of a research publication. This paper explores how the impact (average citations per paper) varies with different types of collaboration. A calibrated bibliometric model is derived that demonstrates that collaborating with an author from the home institution or another domestic institution increases the average impact by approximately 0.75 citations while collaborating with an author from a foreign institution increases the impact by about 1.6 citations.     

Evolution of enzymatic activities in the enolase superfamily: partitioning of reactive intermediates by (D)-glucarate dehydratase from Pseudomonas putida

Glucarate dehydratase (GlucD) from Pseudomonas putida catalyzes the dehydration of both (D)-glucarate and (L)-idarate to 3-deoxy-(L)-threo-2-hexulosarate as well as their epimerization. (D)-[6-13C]Glucarate and (L)-[6-13C]idarate have been synthesized for use in continuous assay of the reactions catalyzed by GlucD by both 13C and 1H NMR spectroscopies, thereby allowing the simultaneous measure of both the dehydration and epimerization reactions. Substrate and solvent isotope effects for the dehydration reactions have been quantitated. The mechanism of the GlucD-catalyzed reaction is discussed in the context of that previously established for the homologous mandelate racemase from P. putida, also a member of the enolase superfamily whose members catalyze reactions initiated by abstraction of a proton alpha to a carboxylate group.     

The product of the herpes simplex virus type 1 UL25 gene is required for encapsidation but not for cleavage of replicated viral DNA

The herpes simplex virus type 1 (HSV-1) UL25 gene contains a 580-amino-acid open reading frame that codes for an essential protein. Previous studies have shown that the UL25 gene product is a virion component (M. A. Ali et al., Virology 216:278-283, 1996) involved in virus penetration and capsid assembly (C. Addison et al., Virology 138:246-259, 1984). In this study, we describe the isolation of a UL25 mutant (KUL25NS) that was constructed by insertion of an in-frame stop codon in the UL25 open reading frame and propagated on a complementing cell line. Although the mutant was capable of synthesis of viral DNA, it did not form plaques or produce infectious virus in noncomplementing cells. Antibodies specific for the UL25 protein were used to demonstrate that KUL25NS-infected Vero cells did not express the UL25 protein. Western immunoblotting showed that the UL25 protein was associated with purified, wild-type HSV A, B, and C capsids. Transmission electron microscopy indicated that the nucleus of Vero cells infected with KUL25NS contained large numbers of both A and B capsids but no C capsids. Analysis of infected cells by sucrose gradient sedimentation analysis confirmed that the ratio of A to B capsids was elevated in KUL25NS-infected Vero cells. Following restriction enzyme digestion, specific terminal fragments were observed in DNA isolated from KUL25NS-infected Vero cells, indicating that the UL25 gene was not required for cleavage of replicated viral DNA. The latter result was confirmed by pulsed-field gel electrophoresis (PFGE), which showed the presence of genome-size viral DNA in KUL25NS-infected Vero cells. DNase I treatment prior to PFGE demonstrated that monomeric HSV DNA was not packaged in the absence of the UL25 protein. Our results indicate that the product of the UL25 gene is required for packaging but not cleavage of replicated viral DNA.     

The effect of pathologic substances and adulterants on the DNA typing of urine

Human urine has not been adequately investigated as a potential source of DNA for forensic identity testing. The advent of polymerase chain reaction technology has made possible the analysis of previously undetectable levels of nucleic acids from human urine and other body fluids lacking nucleated cells. In this study, we evaluated the ability to genotype DNA extracted from adulterated urine specimens using the AmpliType PM + DQA1 PCR amplification and typing system. Fresh, first-void male urine specimens were contaminated with household bleach, E. coli, human serum albumin, glucose and saponin (a strong detergent). All of the adulterated samples were typed without difficulty. Frozen male urine specimens were split into equal volumes; one aliquot was adulterated with either E. coli or saponin, and the other was left free of contaminants. Seventy-one percent of all frozen urine specimens tested (adulterated and unadulterated) were successfully typed using this amplification and typing system. Our data, therefore, suggest that the AmpliType PM + DQA1 PCR amplification and typing system described is suitable for genotype analysis of adulterated fresh and frozen urine specimens.