Phosphorus Dynamics in Cultures and Natural Populations of Trichodesmium spp

Trichodesmium spp. fix atmospheric N2 and so an element other than N limits production by these species in the oligotrophic ocean. Because dissolved inorganic phosphorus (DIP) is in short supply in many marine systems, it has been hypothesized that P is a growth-limiting nutrient for these species in nature. However, Trichodesmium is capable of hydrolyzing dissolved organic P (DOP) compounds and the inorganic products from hydrolysis may provide an additional source of P for growth. We investigated P dynamics and alkaline phosphatase activity in cultures and natural populations of Trichodesmium from the Atlantic Ocean and the north coast of Australia to determine whether hydrolysis of DOP could supply enough P to fuel growth. During the Atlantic cruise, concentrations of DIP were lower and chlorophyll (chl a)-specific rates of alkaline phosphatase activity by Trichodesmium were higher than during the Australian transect. However, because Trichodesmium were much more abundant during the Australian transect, where they represented the bulk of the surface chl a biomass, total water column rates of alkaline phosphatase activity were higher along the Australian transect than in the Atlantic. In both systems, DOP could potentially supply a significant portion of the cellular P necessary for growth. In cultures and natural populations, alkaline phosphatase activity was inhibited when DIP was present and increased in the presence of DOP. Cultures of Trichodesmium IMS101 grew equally well on media enriched with DOP or DIP at all but the highest enrichment levels. From these studies, we conclude that if the supply of appropriate DOP substrates is adequate, DOP can represent an important P source for Trichodesmium growth which should be included in estimates of P availability in surface waters

Routine synthesis of N-[11C-methyl]scopolamine by phosphite mediated reductive methylation with [11C]formaldehyde

A synthesis of [11C]scopolamine capable of clinical delivery of this agent in high specific activity is described. The precursor [11C]formaldehyde was produced by catalytic oxidation of [11C]CH3OH over metallic silver and was used to N-11C-methylate norscopolamine using aqueous neutral potassium phosphite as the reducing agent. The labeling reaction was complete after 5 min at 75-80[deg]C and the [11C]scopolamine (99% radiochemical purity) was isolated by preparative HPLC. Total synthesis time is less than 45 min. Decay corrected radiochemical yields from [11C]CO2 are presently 20-43%.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/27552/1/0000596.pd

Routine production of 2-deoxy-2-[18F]fluoro--glucose by direct nucleophilic exchange on a quaternary 4-aminopyridinium resin

Resin-supported [18F]fluoride ion has been prepared and applied to a rapid, convenient synthesis of [18F]FDG. "No-carrier-added" [18F]fluoride ion is collected on a quaternary 4-(N, N-dialkylamino)-pyridinium functionalized polystyrene anion exchange resin directly from a [18O]water target, dried by rinsing with acetonitrile, and then reacted with 1,3,4,6-tetra-O-acetyl-2-O-trifluoromethanesulfonyl-[beta]--mannopyrannose. Acidic hydrolysis yields [18F]FDG in a synthesis time of 40 min with overall yields presently averaging above 50%.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/28859/1/0000694.pd

Extensive bloom of a N₂-fixing diatom/cyanobacterial association in the tropical Atlantic Ocean

We encountered an extensive bloom of the colonial diatom Hemiaulus hauckii along a 2500 km cruise track off the NE coast of South America in autumn 1996. Each diatom cell contained the heterocystous. N₂-fixing cyanobacterial endosymbiont Richeiia intracellularis. Surface Richeiia heterocyst (and filament) densities increased from 10⁶ heterocyst 1⁻¹ in the bloom. Total abundance ranged from 10⁶ eterocyst m⁻² outside the bloom to over 10¹⁰ heterocyst m⁻² within the bloom. Rates of primary production averaged 1.2 g C m⁻² d⁻¹, higher than typical for oligotrophic Open ocean waters. N₂ fixation during the bloom by the Richelia/Hemiaulus association added an average of 45 mg N m⁻² d⁻¹ to the water column. The relative importance of NH₄⁺ uptake over the Course of the bloom increased from 0 to 42% of total N uptake by the Hemiauluslficheiia association. N₂ fixation by Richelia exceeded estimates of 'new' N flux via NO₃ diffusion from deep water and, together with additional N, fixation by the cyanobacterium Trichodesmium, could supply about 25% of the total N demand through the water column during the bloom. Suspended particles and zooplankton collected within the bloom were depleted in ¹⁵N, reflecting the dominant contribution of N₂ fixation to the planktonic N budget. The bloom was spatially extensive, as revealed by satellite imagery, and is calculated to have contributed about 0.5 Tg N to the euphotic zone. Such blooms may represent an important and previously unrecognized source of new N to support primary production in nutrient-poor tropical waters. Furthermore, this bloom demonstrates that heterocystous cyanobacteria can also make quantitatively important contributions of N in oceanic water column environments

Multiphase extraction: Rapid phase-transfer of [18F]fluoride ion for nucleophilic radiolabeling reactions

In multiphase extraction [18F]fluoride ion for radiolabeling is recovered from target water by passage through a small column of microporous polymer impregnated with a lipophilic cryptand or quaternary ammonium salt. The 18O enriched water can be recovered for reuse. The [18F]fluoride ion-pair is eluted from the column by a small volume of acetonitrile or other organic solvent. Evaporation of the acetonitrile removes traces of water to yield a reactive ion pair for nucleophilic radiofluorination reactions. A wide range of ion-pairs based on K+ or NH4+ cryptands or quaternary ammonium salts can be employed. The method was applied to the synthesis of [18F]FDG.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/27603/1/0000647.pd

A captive solvent method for rapid N-[11C]methylation of secondary amides: Application to the benzodiazepine, 4'-chlorodiazepam (RO5-4864)

[11C]4'-Chlorodiazepam (RO5-4864), for PET studies of peripheral benzodiazepine receptors, was synthesized by alkylation of 1-desmethyl-4'-chlorodiazepam, in a small volume of acetone adsorbed on acrylic yarn, with [11C]methyl iodide in the injection loop of a liquid chromatograph. The reaction mixture was introduced directly onto a small, disposable alumina chromatographic column. Elution with pentane:ethanol gave a product of high chemical and radiochemical purity. A simple heating and cooling device for the injection loop is described.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/27565/1/0000609.pd