pH-dependent release of elements from hardened and non-hardened wood ash.

Bioenergy systems that utilize clean wood feedstocks are becoming more common in western Canada to produce heat and electricity. But, wood combustion leads to ash residuals that need to be managed. Although there is growing interest in value-added uses for these wood ashes, large quantities of wood ashes are currently stockpiled or landfilled. Wood ash may be self-hardened as a pretreatment strategy to improve handling and reduce reactiveness prior to land application. This study determined aqueous concentrations of constituents released from wood bottom ash (BA) and hardened wood bottom ash (HBA) when subjected to increasing levels of acidity (pH 10 to 4). Such acidic conditions are not common but may exist during some storage, landfilling or land reclamation scenarios. Acidification of BA and HBA increased aqueous concentrations of B, Ca, Cd, Co, Cu, Mg, Mn, Ni, Sr, and Zn, whereas Cr, Hg and Mo showed decreased concentrations. Hardening reduced aqueous concentrations of As, Ca, Co, Fe, Ni, P, and Pb, in HBA compared to BA over a pH range. When properly managed, hardened and non-hardened bottom ashes generated from the combustion of clean wood should pose minimal risk to the environment.

Mobility of biomass ash constituents as influenced by pretreatment and soil - An artificial weathering study.

Biomass ashes are potential soil amendments that reduce soil acidity and provide plant nutrients, but trace elements in ash may be leached from the solid phase, thereby posing environmental concerns. We determined the leachability of selected major elements, trace elements and anions from wood derived bottom ash generated from an updraft gasifier as influenced by ash pretreatments and the presence of soil via serial aqueous batch extraction. We found that self-hardening reduced initial solubility and reactivity of ash (i.e. lowered electrical conductivity), and reduced initial aqueous concentrations of Ba, Ca, Cu, Fe, Hg, Pb, Sr and Zn. But, hardening of ash increased initial aqueous concentrations of B, Cr, P, Se and SO42-. Although mixing ash into soil (5% ash by mass) generally decreased the mobility of most constituents, aqueous concentrations of P and As were increased relative to that of either ash-alone or soil-alone treatments. Overall, extract concentrations of constituents in various treatments were relatively low. Results of this serial batch extraction support the use of clean wood-derived bottom ash as a safe and environmentally suitable soil amendment.

Small molecule inhibitors of yeast pre-mRNA splicing.

The spliceosome catalyzes pre-messenger RNA (pre-mRNA) splicing, an essential process in eukaryotic gene expression in which non-protein-coding sequences are removed from pre-mRNA. The spliceosome is a large, molecular complex composed of five small nuclear RNAs (snRNAs) and over 100 proteins. Large-scale rearrangements of the snRNAs and their associated proteins, including changes in base-pairing partners, are required to properly identify the intron-containing pre-mRNA, position it within the spliceosome, and complete the cleavage and ligation reactions of splicing. Despite detailed knowledge of the composition of the spliceosome at various stages of assembly, the critical signals and conformational changes that drive the dynamic rearrangements required for pre-mRNA splicing remain largely unknown. Just as ribosome-binding antibiotics facilitated mechanistic studies of the ribosome, study of the catalytic mechanisms of the spliceosome could be enhanced by the availability of small molecule inhibitors that block spliceosome assembly and splicing at defined stages. We sought to identify inhibitors of Saccharomyces cerevisiae splicing by screening for small molecules that block yeast splicing in vitro. We identified 10 small molecule inhibitors of yeast splicing, including four antibiotics, one kinase inhibitor, and five oxaspiro compounds. We also report that a subset of the oxaspiro derivatives permitted assembly of spliceosomal complexes onto pre-mRNA but blocked splicing prior to the first cleavage reaction.

Synthesis of two repeat units corresponding to the backbone of the pectic polysaccharide rhamnogalacturonan I.

A tetrasaccharide corresponding to a sequence of the rhamnogalacturonan I backbone has been synthesized. This synthesis relies on only two protected monosaccharides and proceeds through a common disaccharide intermediate. Synthesis of this tetrasaccharide has been designed to allow for the addition of branching elements at the 4-positions of the rhamnosyl units, or further chain elongation at the 2-position.

Synthesis of a disaccharide fragment of rhamnogalacturonan II.

A disaccharide portion of the A-side chain of the rhamnogalacturonan II oligosaccharide has been prepared. Glycosylation of methyl (methyl 3,4-O-isopropylidene-alpha-D-galactopyranosid)uronate with p-tolyl 2,3-di-O-acetyl-3-C-(benzyloxymethyl)-1-thio-alpha/beta-D-erythrofuranoside was carried out using N-iodosuccinimide as promoter and silver trifluoromethanesulfonate as catalyst. Removal of the protecting groups gave the beta-d-Apif-(1-->2)-alpha-D-GalpA-OMe disaccharide.