In this paper, results of an analysis to assess the potential of concentrating solar thermal power applications in Canada are presented. First, a direct normal solar resource (DNI) resource map for Canada is introduced. This map indicates the locations where the DNI is the highest in Canada and is derived from the most recent Perez's SUNY satellite-based solar resource model Version number 3. Second, the methodology and results of a GIS analysis to identify the locations of the most suitable lands for concentrating solar thermal power (CSP) applications in Canada are discussed. The total areas of the CSP-suitable lands are presented in a tabulated and a map formats for each of the Canadian provinces where there is a maximum DNI solar resource. Third and finally, results of a technical economical analysis for two CSP system designs are discussed. The two CSP systems considered include parabolic trough with synthetic oil heat transfer fluid with and without storage, molten salt power tower with and without storage

Ure2p is the precursor protein of the Saccharomyces cerevisiae prion [URE3]. Ure2p shows homology to glutathione transferases but lacks typical glutathione transferase activity. A recent study found that deletion of the Ure2 gene causes increased sensitivity to heavy metal ions and oxidants, whereas prion strains show normal sensitivity. To demonstrate that protection against oxidant toxicity is an inherent property of native and prion Ure2p requires biochemical characterization of the purified protein. Here we use steady-state kinetic methods to characterize the multisubstrate peroxidase activity of Ure2p using GSH with cumene hydroperoxide, hydrogen peroxide, or tert-butyl hydroperoxide as substrates. Glutathione-dependent peroxidase activity was proportional to the Ure2p concentration and showed optima at pH 8 and 40 °C. Michaelis-Menten behavior with convergent straight lines in double reciprocal plots was observed. This excludes a ping-pong mechanism and implies either a rapid-equilibrium random or a steady-state ordered sequential mechanism for Ure2p, consistent with its classification as a glutathione transferase. The mutant 90Ure2, which lacks the unstructured N-terminal prion domain, showed kinetic parameters identical to wild type. Fibrillar aggregates showed the same level of activity as native protein. Demonstration of peroxidase activity for Ure2 represents important progress in elucidation of its role in vivo. Further, establishment of an in vitro activity assay provides a valuable tool for the study of structure-function relationships of the Ure2 protein as both a prion and an enzyme.