Genetic determinants of Rous sarcoma virus particle size

The Gag proteins of retroviruses are the only viral products required for the release of membrane-enclosed particles by budding from the host cell. Particles released when these proteins are expressed alone are identical to authentic virions in their rates of budding, proteolytic processing, and core morphology, as well as density and size. We have previously mapped three very small, modular regions of the Rous sarcoma virus (RSV) Gag protein that are necessary for budding. These assembly domains constitute only 20% of RSV Gag, and alterations within them block or severely impair particle formation. Regions outside of these domains can be deleted without any effect on the density of the particles that are released. However, since density and size are independent parameters for retroviral particles, we employed rate-zonal gradients and electron microscopy in an exhaustive study of mutants lacking the various dispensable segments of Gag to determine which regions would be required to constrain or define the particle dimensions. The only sequence found to be absolutely critical for determining particle size was that of the initial capsid cleavage product, CA-SP, which contains all of the CA sequence plus the spacer peptides located between CA and NC. Some regions of CA-SP appear to be more important than others. In particular, the major homology region does not contribute to defining particle size. Further evidence for interactions among CA-SP domains was obtained from genetic complementation experiments using mutant deltaNC, which lacks the RNA interaction domains in the NC sequence but retains a complete CA-SP sequence. This mutant produces low-density particles heterogeneous in size. It was rescued into particles of normal size and density, but only when the complementing Gag molecules contained the complete CA-SP sequence. We conclude that CA-SP functions during budding in a manner that is independent of the other assembly domains.     

Properties of laterite aggregate concrete

The paper presents the results of tests conducted on fresh and hardened concrete using laterite as aggregate. Several mixes of laterite aggregate concrete were made with varying watercement and aggregate-cement ratios to study the properties like workability, compressive, flexural, tensile strength and Modulus of elasticity. The tests indicate that the workability decreases with increasing aggregate-water ratio. The compressive strength of laterite aggregate concrete is considerably lower than that of gravel or crushed granite aggregate concrete, while the average ratio of cylinder to cube strength compared favourably with that for normal aggregate concrete, for the range of aggregate and water-cement ratios covered in this investigation.     

Cool-down of foam insulated cryogenic transfer lines

An experimental programme is presented for estimating cool-down time for foam insulated cryogenic transfer lines. The results show that there is good agreement between theoretical and experimental cool-down curves. The integral method is shown to be an accurate way to determine the position of cooling front as the cool-down proceeds. It was also found that the mass flow rate does not significantly affect the cool-down of short transfer lines.     

X-ray studies on the thermal expansion of tellurium dioxide

Using a Unicam 19 cm high temperature powder camera, the precision lattice parameters of tellurium dioxide have been determined at different temperatures in the range 30 to 461 °C. Using this data, the coefficients of thermal expansion, and parallel and perpendicular to the principal axis respectively, have been evaluated. The temperature dependence of the coefficients of thermal expansion is represented by the following equations: =29.673×10^–6+1.552sx10^–8 T+1.069sx10^–10 T ² =9.875sx10^–6–5.440sx10^–9 T+4.572sx 10^–12 T² HereT is the temperature in °C. The thermal expansion of tellurium dioxide has been explained in terms of the interionic distances.     

Cyclodextrin-Enhanced Electrokinetic Remediation of Soils Contaminated with 2,4-Dinitrotoluene

The removal of 2,4-dinitrotoluene (2,4-DNT), a munitions waste constituent and an industrial intermediate, from contaminated soils was evaluated using enhanced electrokinetic (EK) remediation. Two model soils were spiked with 480?mg of 2,4-DNT/kg of dry soil for the EK experiments. The spiked soils were kaolin, a low-buffering clayey soil, and glacial till, a high-buffering silty soil. The glacial till was obtained from a field site and contained 2.8% organic matter. Deionized (DI) water and cyclodextrin solutions were used as the EK purging solutions. Cyclodextrin was selected as a nonhazardous solubility enhancer for enhancing the desorption and removal of 2,4-DNT from soils in EK remediation. Two aqueous solutions of hydroxypropyl β-cyclodextrin (HPCD) at concentrations of 1 and 2% were selected for kaolin and glacial till, respectively, based on results for batch extraction of 2,4-DNT from the same soils. During the EK experiments, greater current and electro-osmotic flow were observed for HPCD solutions than for DI water. After the completion of the EK experiments, the soils in the EK cell were extruded and the residual 2,4-DNT in the soils was determined. Less 2,4-DNT remained in the kaolin soil (up to 94% transformed) than in the glacial till soil (20% transformed) due to strong retention of 2,4-DNT by the soil organic matter in glacial till. For kaolin, less 2,4-DNT remained in the soil using HPCD solutions than using DI water. For glacial till, comparable levels of 2,4-DNT remained in the soil for both EK solutions. Since no 2,4-DNT was detected in the effluents from the EK cells, the decrease in 2,4-DNT concentration in the kaolin and glacial till soils was attributed to electrochemical transformation of 2,4-DNT to other species.     

Phase equilibria for iron-rich Fe−Cu−C alloys: 1500 to 950°C

Isothermal sections for the iron rich corner of the Fe−Cu−C system have been constructed at 1500, 1450, 1200, 1172, 1150, 1000, and 950°C. A ternary invariant point exists at 1172°C where an iron rich liquid, a copper rich liquid, austenite, and graphite coexist. The iron rich liquid contains 3.7 wt pct Cu and 4.0 wt pct C. The austenite contains 7.3 pct Cu and 1.6 pct C. The copper rich liquid contains 2.4 pct Fe, and apparently very little carbon. The diagrams are used to explain the phenomena of “inverse segregation” that occurs during the solidification of iron rich Fe−Cu−C alloys. KRISHNA PARAMESWARAN, formerly Metallurgy Graduate Student, University of Missouri-Rolla KENNETH METZ, formerly Metallurgy Graduate Student, University of Missouri-Rolla     

Folding of the glucocorticoid receptor by the heat shock protein (hsp) 90-based chaperone machinery. The role of p23 is to stabilize receptor.hsp90 heterocomplexes formed by hsp90.p60.hsp70

In cytosols from animal and plant cells, the abundant heat shock protein hsp90 is associated with several proteins that act together to assemble steroid receptors into receptor.hsp90 heterocomplexes. We have reconstituted a minimal receptor.hsp90 assembly system containing four required components, hsp90, hsp70, p60, and p23 (Dittmar, K. D., Hutchison, K. A., Owens-Grillo, J. K., and Pratt, W. B. (1996) J. Biol. Chem. 271, 12833-12839). We have shown that hsp90, p60, and hsp70 are sufficient for carrying out the folding change that converts the glucocorticoid receptor (GR) hormone binding domain (HBD) from a non-steroid binding to a steroid binding conformation, but to form stable GR.hsp90 heterocomplexes, p23 must also be present in the incubation mix (Dittmar, K. D., and Pratt, W. B. (1997) J. Biol. Chem. 272, 13047-13054). In this work, we show that addition of p23 to native GR.hsp90 heterocomplexes immunoadsorbed from L cell cytosol or to GR.hsp90 heterocomplexes prepared with the minimal (hsp90.p60.hsp70) assembly system inhibits both receptor heterocomplex disassembly and loss of steroid binding activity. p23 stabilizes the GR.hsp90 heterocomplex in a dynamic and ATP-independent manner. In contrast to hsp90 that is bound to the GR, free hsp90 binds p23 in an ATP-dependent manner, and hsp90 in the hsp90.p60.hsp70 heterocomplex is in a conformation that does not bind p23 at all. The effect of p23 in the minimal GR heterocomplex assembly system is to stabilize GR.hsp90 heterocomplexes once they are formed and it does not appear to affect the rate of heterocomplex assembly. Molybdate has the same ability as p23 to stabilize GR heterocomplexes with mammalian hsp90, but GR heterocomplexes with plant hsp90 are stabilized by p23 and not by molybdate. We propose that incubation of the GR with hsp90.p60.hsp70 forms a GR.hsp90 heterocomplex in which hsp90 is in an ATP-dependent conformation. The ATP-dependent conformation of hsp90 is required for the hormone binding domain to have a steroid binding site, and binding of p23 to that state of hsp90 stabilizes the GR.hsp90 heterocomplex to inactivation and disassembly.     

The effect of line configuration on perceived numerosity of dotted lines

Estimates the number of objects in a line are made in many different situations. This paper demonstrates that besides the actual number of dots, aspects of line configuration affect the perceived numerosity of dotted lines. Experiment 1 provides evidence that the highly studied "clutter effect" in distance perception research replicates to the numerosity domain so that lines made up of more segments are perceived to contain more dots. Experiments 2-5 provide nomological validity for the recently proposed "direct distance" effect in distance perceptions by showing that numerosity perceptions are higher the greater the euclidean length between the line end points and by manipulating euclidean length in three orthogonal ways: the relative length of segments (Experiment 2), the angle between segments (Experiment 3), and the general direction of segments (Experiment 4). Experiment 5 conceptually replicates the results of Experiments 2-4 utilizing stimuli-based versus memory-based judgments and a discrimination task. Experiments 6 and 7 extend the research on spatial perception by demonstrating that the use of euclidean length as a source of information is inversely related to line width, with width varied through clutter (Experiment 6) and total line length (Experiment 7). Overall, the results demonstrate that the robustness of the euclidean length effect is contingent on the salience of alternative spatial heuristics--specifically, euclidean width. Theoretical implications are discussed.     

Fenton-Like Oxidation of Polycyclic Aromatic Hydrocarbons in Soils Using Electrokinetics

An integrated electrochemical oxidation process that utilizes electrokinetics (EK) to deliver the oxidant (5–10% hydrogen peroxide, H2O2) and chelant [40 mM of ethylenediaminetetraacetic acid (EDTA) or diethylenetriaminepentaacetic acid (DTPA)] or iron chelate (1.4 mM Fe-EDTA or Fe-DTPA) to oxidize polycyclic aromatic hydrocarbons (PAHs) in soils was investigated. Batch and bench-scale EK experiments were conducted using: (a) kaolin, a low permeability clayey soil, spiked with phenanthrene at 500 mg/kg, and (b) former manufactured gas plant (MGP) soil, a high buffering silty soil, contaminated by a variety of PAHs (1493 mg/kg). Batch experiments showed that chelant solutions dissolve native iron minerals to form soluble Fe-chelates that remain available even at higher pH conditions of soil for the Fenton-like oxidation of the PAHs. In EK experiments, a 5–10% H2O2 solution was delivered from the anode and a chelant solution or iron-chelate was delivered from the cathode. Preflushing of soil with 5% ethanol and ferrous sulfate (1.4 mM) prior to oxidant delivery was also investigated. An electric potential of 2 VDC/cm was applied in all tests to induce electroosmotic flow for 5–8 days for kaolin and 25 days for the MGP field soil. In the absence of any chelating agent, phenanthrene oxidation was catalyzed by native iron present in kaolin soil, and 49.8–82.3% of phenanthrene was oxidized by increasing H2O2 concentration from 5–10%. At 5% H2O2 concentration, phenanthrene oxidation was not increased by using 40 mM EDTA, 40 mM DTPA or 1.4 mM Fe-DTPA, but it increased to 70% using 1.4 mM Fe-EDTA. Maximum phenanthrene oxidation (90.5%) was observed by 5% ethanol preflushing and then treating with 5% H2O2 at the anode and 1.4 mM Fe-EDTA at the cathode. However, preflushing with 1.4 mM ferrous sulfate did not improve phenanthrene oxidation. The results with the MGP field soil indicated that delivery of 5% H2O2 alone resulted in oxidation of 39.8% of total PAHs (especially 2- and 3-ring PAHs). The use of EDTA and Fe-EDTA did not increase PAHs oxidation in this soil. Overall, the results reveal that an optimized in situ combined technology of EK and Fenton-like process has the potential to oxidize PAHs in low permeability and/or high buffering soils.