On the mechanism of enzyme action. XLV. The role of certain dicarboxylic acids in the formation of oxalic acid by wood-destroying molds

Alkalinity of the medium was shown to be the chief factor involved in the accumulation of oxalate by T. cinnabarina. Glutamate and aspartate are shown to lead to oxalate with this organism and with L. lepideus by dehydrogenation to α-ketoglutarate and oxaloacetate, respectively. Malate was also shown to be dehydrogenated. It is proposed that oxaloacetate may either undergo β-decarboxylation to yield CO₂ and pyruvate, or splitting by coenzyme A to yield oxalate and acetylated coenzyme A. The reversal of this latter reaction is suggested as the explanation of the disappearance of oxalate from culture media. The reduction of resazurin by the dehydrogenase systems of the molds is inhibited by cyanide, indicating the participation of metal systems, such as the cytochromes.     

Critical Inuit Studies: An Anthology of Contemporary Arctic Ethnography

Critical Inuit Studies: An Anthology of Contemporary Arctic Ethnography . Pamela Stern and Lisa Stevenson, eds. Lincoln: Nebraska University Press, 2006. 302 pp.     

Identification of a second distinct strain of beet mild yellowing luteovirus using monoclonal antibodies and transmission studies

The variation among isolates of beet mild yellowing luteovirus (BMYV), collected from commercial crops of sugar beet during 1990, 1992 and 1993, was studied using monoclonal antibodies and transmissions to indicator species. The common strain of BMYV, which occurs throughout the sugar-beet root growing area, reacts with monoclonal antibodies MAFF 24, BWYV-BC-510H and BYDV-PAV-IL-1, and infects Capsella bursa-pastoris. A second strain, which failed to react with monoclonal antibody BYDV-PAV-IL-1 and which did not infect C. bursa-pastoris, was identified in 11% of sampled infected plants. The implications of the properties of this strain for the epidemiology of BMYV are discussed.     

Glucose-6-phosphate Dehydrogenase Activity under Conditions of Water Limitation: a Possible Model System for Enzyme Reactions in Unimbibed Resting Seeds and its Relevance to Seed Viability

A model system has been used to measure glucose-6-phosphatedehydrogenase (G-6-PDH) activity when the water contents ofthe reactants are comparable to the water contents of dry restingseeds. The activity of G-6-PDH is reduced by 10²–10³ whenthe water content is limited to between 1.5 and 25 per cent.G-6-PDH activity is affected by temperature and by the proteincontent of the model system. The glucose 6-phosphate (7.03 nmolg^–1 embryo) and the NADP⁺ (25.0 nmol g^–1 embryo)contents of barley embryos were measured. Using these measurements,together with the measurements in the model system of G-6-PDHactivity at low water concentrations, an estimate is made ofthe G-6-PDH activity in resting barley embryo. A cor-relationbetween estimated G-6-PDH activity at different water contentsand the periods for which seeds remain viable is indicated.The limitations of the model system are discussed.     

The significance of alkaline phosphatase activity in Lough Neagh

SUMMARY. A study of the eutrophic Lough Neagh was undertaken to ascertain the use of alkaline phosphatase activity as an indicator of phosphorus-limited algal growth. Lough Neagh and its surrounding rivers were monitored during 1974 and 1975. Alkaline phosphatase activity increased in the lough when the algal crop increased and depleted orthophosphate to a growth-limiting concentration. Enzyme activity was appreciable, however, at all other times of the year and may on occasions have been associated with zooplankton. The enzyme activity in the inflowing rivers was much greater than in the lough itself. Depending on enzyme stability the enzyme inputs from rivers could contribute significantly to the lough activity. Sewage disposal works effluent appeared to be a major source of enzyme activity in river water. As the alkaline phosphate activity in Lough Neagh resulted from several sources, increased activity could not be used as a reliable indicator of phosphorus limited algal growth.