Mg2؉ -dependent phosphatidate (PA) phosphatase (3-sn-phosphatidate phosphohydrolase, EC 3.1.3.4) catalyzes the dephosphorylation of PA to yield diacylglycerol and P i . In this work, we identified the Saccharomyces cerevisiae PAH1 (previously known as SMP2) gene that encodes Mg 2؉ -dependent PA phosphatase using amino acid sequence information derived from a purified preparation of the enzyme (Lin, Y.-P., and Carman, G. M. (1989) J. Biol. Chem. 264, 8641-8645). Overexpression of PAH1 in S. cerevisiae directed elevated levels of Mg 2؉ -dependent PA phosphatase activity, whereas the pah1⌬ mutation caused reduced levels of enzyme activity. Heterologous expression of PAH1 in Escherichia coli confirmed that Pah1p is a Mg 2؉ -dependent PA phosphatase enzyme and showed that its enzymological properties were very similar to those of the enzyme purified from S. cerevisiae. The PAH1-encoded enzyme activity was associated with both the membrane and cytosolic fractions of the cell, and the membrane-bound form of the enzyme was salt-extractable. Lipid analysis showed that mutants lacking PAH1 accumulated PA and had reduced amounts of diacylglycerol and its derivative triacylglycerol. The PAH1-encoded Mg 2؉ -dependent PA phosphatase shows homology to mammalian lipin, a fat-regulating protein whose molecular function is unknown. Heterologous expression of human LPIN1 in E. coli showed that lipin 1 is also a Mg 2؉ -dependent PA phosphatase enzyme.

5Previously we revealed that the high toughness of double network hydrogels (DN gels) derives from the internal fracture of the brittle network during deformation, which dissipates energy as sacrificial bonds. In this study, we intend to elucidate the detailed internal fracture process of DN gels. We quantitatively analysed the tensile hysteresis and re-swelling behaviour of a DN gel that shows a well-defined necking and strain hardening, and obtained the following new findings: 1) Fracture of the 1 st network PAMPS 10 starts far below the yielding strain, and 90% of the initially load-bearing PAMPS chains already breaks at the necking point.2) The dominant internal fracture process occurs in the necking and hardening region although the softening mainly occurs before necking.3) The internal fracture efficiency is very high, 85% of the work is used for the internal fracture and 9% of all PAMPS chains break at sample failure. 4) The internal fracture is anisotropic, fracture occurs preferentially perpendicular to the tensile direction than 15 other two directions, but the fracture anisotropy decreases in the hardening region. Result 1) and 2) is in agreement with a hierarchical structural model of PAMPS network. Based on these findings, we present a revised description of the fracture process of DN gels.

The frequency and energy dissipation change of a quartz crystal microbalance during moisture absorption was measured for films with thickness ranging from 3 to 205 nm. Evidence of the viscoelastic nature of the films was observed for films thicker than 90 nm through the frequency and energy dissipation changes. For sufficiently thin films (t < 40 nm), the frequency change could be effectively modeled as a simple increase in mass, as predicted by the Sauerbrey equation. The viscosity of the swollen films was independent of initial polymer film thickness (93-205 nm). The equilibrium swelling ratio was independent of film thickness for all films examined (3-205 nm). The transition between the observation of a rigid film and a film showing viscoelastic character was found to be at β 1 D ) 0.26 ( 0.10, where β 1 ) 2π/λ s , λ s is the shear wavelength, and D is the film thickness. This transition agrees with the predictions of White and Schrag (J. Chem. Phys. 1999, 111, 11192).

The purpose of this work was to determine the influence of chemical food-simulating liquids on the wear of various commercial dental composite restoratives. In many cases, pre-conditioning the restoratives in these liquids for one week produced swelling of the polymer matrix and considerable surface damage. The resulting degradation reduced the hardness and enhanced the wear as measured by a pin-and-disc apparatus. Four kinds of commercial composites were investigated: a conventional quartz-filled, a strontium-glass-filled, a visible-light-activated, and a microfilled composite. The liquids employed were heptane and several aqueous solutions of ethanol with solubility parameters, delta, ranging from delta = 1.5 to 4.8 X 10(4) J1/2m-3/2. With all restoratives, the decline in hardness during pre-conditioning maximized at about delta = 3 X 10(4), which corresponds to a 75% ethanol solution. The wear behavior was considerably more complicated and variable, as discussed in the text. For the most part, the increase in wear rate from pre-conditioning corresponded to the fall in hardness. A notable exception was for the strontium-glass-filled composite pre-conditioned in pure water. Here the wear was enhanced considerably, with no decrease in hardness. In this case, the degradation mode is assumed to be different from the others in that it is attributed to stress corrosion of the glass filler.

Specular X-ray reflectivity (XR) and quartz crystal microbalance (QCM) measurements were used to determine the absorption of water into thin poly(4-ammonium styrenesulfonic acid) films from saturated vapor at 25 degrees C. The effect of film thickness on the absorption kinetics and overall absorption was investigated in the range of thickness from (3 to 200) nm. The equilibrium swelling of all the films irrespective of film thickness was (0.57+/-0.03) volume fraction. Although the equilibrium absorption is independent ofthickness, the absorption rate substantially decreases for film thickness < 100 nm. For the thinnest film (3 nm), there is a 5 orders of magnitude decrease in the diffusion coefficient for water.