11,078 research outputs found
Mobilization of a trapped non-wetting fluid from a three-dimensional porous medium
We use confocal microscopy to directly visualize the formation and complex
morphologies of trapped non-wetting fluid ganglia within a model 3D porous
medium. The wetting fluid continues to flow around the ganglia after they form;
this flow is characterized by a capillary number, Ca. We find that the ganglia
configurations do not vary for small Ca; by contrast, as Ca is increased above
a threshold value, the largest ganglia start to become mobilized and are
ultimately removed from the medium. By combining our 3D visualization with
measurements of the bulk transport, we show that this behavior can be
quantitatively understood by balancing the viscous forces exerted on the
ganglia with the pore-scale capillary forces that keep them trapped within the
medium. Our work thus helps elucidate the fluid dynamics underlying the
mobilization of a trapped non-wetting fluid from a 3D porous medium
alpha -Lactalbumin (LA) Stimulates Milk beta-1,4-Galactosyltransferase I (beta 4Gal-T1) to Transfer Glucose from UDP-glucose to N-Acetylglucosamine: CRYSTAL STRUCTURE OF beta 4Gal-T1·LA COMPLEX WITH UDP-Glc*
beta-1,4-Galactosyltransferase 1 (Gal-T1) transfers galactose (Gal) from UDP-Gal to N-acetylglucosamine (GlcNAc), which constitutes its normal galactosyltransferase (Gal-T) activity. In the presence of alpha -lactalbumin (LA), it transfers Gal to Glc, which is its lactose synthase (LS) activity. It also transfers glucose (Glc) from UDP-Glc to GlcNAc, constituting the glucosyltransferase (Glc-T) activity, albeit at an efficiency of only 0.3-0.4% of Gal-T activity. In the present study, we show that LA increases this activity almost 30-fold. It also enhances the Glc-T activity toward various N-acyl substituted glucosamine acceptors. Steady state kinetic studies of Glc-T reaction show that the Km for the donor and acceptor substrates are high in the absence of LA. In the presence of LA, the Km for the acceptor substrate is reduced 30-fold, whereas for UDP-Glc it is reduced only 5-fold. In order to understand this property, we have determined the crystal structures of the Gal-T1·LA complex with UDP-Glc·Mn2+ and with N-butanoyl-glucosamine (N-butanoyl-GlcN), a preferred sugar acceptor in the Glc-T activity. The crystal structures reveal that although the binding of UDP-Glc is quite similar to UDP-Gal, there are few significant differences observed in the hydrogen bonding interactions between UDP-Glc and Gal-T1. Based on the present kinetic and crystal structural studies, a possible explanation for the role of LA in the Glc-T activity has been proposed
Competition between Superconductivity and Charge Density Wave Ordering in the LuIr(SiGe) Alloy System
We have performed bulk measurements such as dc magnetic susceptibility,
electrical resistivity and heat capacity on the pseudo-ternary alloys
LuIr(SiGe) to study the interplay and competition
between superconductivity and the charge density wave (CDW) ordering
transition. We track the evolution of the superconducting transition
temperature T and the CDW ordering temperature T as a function
of x (concentration of Ge) (). We find that increasing x
(increasing disorder) suppresses the T rapidly with the concomitant
increase in T. We present a temperature-concentration (or volume) phase
diagram for this system and compare our results with earlier work on
substitution at the Lu or Ir site to show how dilution at the Si site presents
a different situation from these other works. The heat capacity data in the
vicinity of the CDW transition has been analyzed using a model of critical
fluctuations in addition to a mean-field contribution and a smooth lattice
background. We find that the critical exponents change appreciably with
increasing disorder. This analysis suggests that the strong-coupling and non
mean-field like CDW transition in the parent compound LuIrSi
changes to a mean-field like transition with increasing Ge concentration.Comment: 14 pages and 8 figures. Accepted for publication in Phys. Rev.
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