4 results match your criteria: "University of Wales at Cardiff[Affiliation]"
Angew Chem Int Ed Engl
September 2001
Department of Chemistry, University of Leuven Celestijueleua 200F, 3001 Leuven (Belgium) Fax: (+32) 16-32-79-92.
Only the 1,2-diphosphacyclobutadiene and none of its 1,3 isomer was obtained in the reaction of 1 with tBuC≡P to give 2. In complex 1, which was prepared from [TaCl (η -C Me )(CO) (thf)] and tBuC≡P, the phosphaalkyne adopts an η (4e) bonding mode according to NMR data, crystal structure analysis, and theoretical calculations.
View Article and Find Full Text PDFJ Theor Biol
July 2000
Welsh School of Pharmacy, University of Wales at Cardiff, Redwood Building, King Edward VII Avenue, Cardiff, CF1 3XF, U.K.
Steady-state solutions are developed for the rate of G alpha.GTP production in a synthase model of the ligand-receptor-G-protein ternary complex activated by a ligand-receptor proton pumping mechanism. The effective rate, k(31), defining the proton transfer, phosphorylation and G alpha.
View Article and Find Full Text PDFCytometry
March 1999
School of Pure and Applied Biology, University of Wales at Cardiff, United Kingdom.
Background: Conventional techniques used to assess bactericidal activities of antibodies are time-consuming; flow cytometry has been used as a rapid alternative. In this study, the membrane potential-sensitive fluorescent probes bis-(1,3-dibutylbarbituric acid) trimethine oxonol (DiBAC4(3)) and Sytox Green, the redox dye cyano-2,3-ditolyl tetrazolium chloride (CTC), and the Baclite viability test kit were used to assess the effects of ceftazidime, ampicillin, and vancomycin on clinical isolates of Pseudomonas aeruginosa, Escherichia coli, and Staphylococcus aureus, respectively.
Methods: Bacterial cultures were grown to early exponential phase, at which point the antibiotics were added at their breakpoint values, and incubation was allowed to continue.
Eur J Biochem
March 1996
School of Molecular and Medical Biosciences, University of Wales at Cardiff, Wales.
Two different mechanisms have been proposed previously for initiating the biodegradation of monomethyl sulfate (MeSO4) in bacteria. For a Hyphomicrobium species, a sulfatase enzyme has been proposed to hydrolyse MeSO4 to methanol and inorganic sulfate. For an Agrobacterium sp.
View Article and Find Full Text PDF