Synthesis and characterization of phi-type zeolites LZ-276 and LZ-277: faulted members of the ABC-D6R family of zeolites

A new zeolite, LZ-276, was synthesized in an organic (TEAOH) system by varying the crystallization temperature in the procedure used by Jacobs and Martens for the synthesis of zeolite phi. LZ-276 (with SiO₂/Al₂O₃=7.8) is more siliceous than phi. Another silicon-rich zeolite, LZ-277 (SiO₂/Al₂O₃=6.6), was synthesized in a totally inorganic system. The similar chemical and physical properties of LZ-276 and LZ-277 are compared with those of zeolite phi described by Grose and Flanigen, and others. TEM [100] selected area diffraction patterns of LZ-277 can be indexed on a hexagonal unit cell with a=13.8 and c=15 Å. Twin spots and considerable streaking parallel to {00l} indicate mirror faulting along c. High resolution images on selected crystals of LZ-277 show that the most closely spaced mirror faults occur approximately every 18 Å. The bulk X-ray sample of LZ-276 is less faulted. A close match between the experimental synchrotron X-ray powder diffraction pattern of LZ-276 and one simulated by the DIFFaX program (with faulting probability=10%) indicates that the structures of these materials can be described as a chabazite (CHA) topology with faulting along c, the stacking direction in these ABC double six-ring (D6R) materials. The distribution of interior cages, including new larger cages that result from faulting, is presented.     

A backstepping‐based low‐and‐high gain design for marine vehicles

A backstepping control design for marine vehicles was described in (Marine Control Systems: Guidance, Navigation and Control of Ships, Rigs, and Underwater Vehicles. Marine Cybernetics AS: Trondheim, Norway, 2002). Under a backstepping feedback law, global asymptotic stability of the closed‐loop system can be shown under the assumption of unlimited actuation. This paper addresses the issues that arise in the implementation of a backstepping feedback law by saturating actuators. First, for a given backstepping feedback law, an estimate of the domain of attraction is given for the resulting closed‐loop system under actuator saturation. A high gain component is then constructed and augmented to the original backstepping feedback law. This additional high gain component is shown not to shrink the estimate of the domain of attraction but to possess the ability to improve the closed‐loop response and to reject disturbance. Copyright © 2008 John Wiley & Sons, Ltd.     

Optimal concentrations of lysine, methionine, and threonine in milk replacers for calves less than five weeks of age

The AA requirements of herd-replacement calves less than 5 wk old and fed milk replacers are not clearly defined and have been estimated in a limited number of studies using milk-fed calves ranging from 5 to 20 wk of age. The objective of these 4 studies was to investigate the effect of supplementing milk replacers containing 24 to 28% crude protein (CP; from milk sources) and 17% fat with Lys, Met, and Thr to estimate the optimum requirements for calves less than 5 wk of age. Holstein bull calves (initially 3 and 4 d old, 43 ± 1 kg of body weight, BW) were fed an 18% CP (as-fed) starter ad libitum and weaned at 31 to 32 d of age (28-d studies). Calves were housed in an unheated, curtain-sided nursery. In study 1, 6 milk replacer treatments were fed based on the combination of 3 CP concentrations (24, 26, and 28% CP) each with or without added Lys and Met. In studies 2 and 3, 26% CP and 2.34% Lys milk replacer treatments were fed to test the concentration of Met (0.64, 0.68, and 0.72% Met in study 2 and 0.64, 0.72, and 0.80% Met in study 3). In study 4, 26% CP, 2.34% Lys, and 0.72% Met milk replacer treatments were fed to test the concentration of Thr (1.06, 1.43, and 1.80%). There was a 17% improvement in average daily gain (ADG) in study 1 from adding Lys and Met that was maximized with 2.34% Lys. The ADG response to added Met in studies 2 (linear) and 3 (quadratic) were 13 and 7%, respectively, with a plateau at 0.72% Met. There was no ADG or efficiency response to added Thr in study 4. Formulating 17% fat, whey-based milk replacers fed at 0.68 kg/d to 26% CP, 2.34% Lys, and 0.72% Met appeared optimum based on responses of body weight gain, feed efficiency, and serum concentrations of urea nitrogen, while feeding calves more CP and essential AA did not improved ADG and efficiency. Requirements for calves less than 5 wk old, averaging 48 kg of BW, consuming 204 g of CP/d, and gaining 0.46 kg of BW/d, appeared to be met with 17 g of Lys, 0.31 Met:Lys ratio, 0.54 Met+Cys:Lys ratio, and a Thr:Lys ratio less than 0.60.     

Effects of feeding different carbohydrate sources and amounts to young calves

Corn, oats, molasses, and soyhulls are commonly used carbohydrate sources in calf starters. A total of 180 calves were used in 4 studies to compare the use of these ingredients in calf starters. Study 1 compared textured starters with different amounts of molasses or sucrose. The control starter contained 5% molasses (A). The test starters contained greater concentrations of dietary sugar than starter A as either 10% molasses (B) or 5% molasses plus 1.5% granular sucrose (C). Starters B and C were equal in dietary sugar. Study 2 evaluated textured starters containing 0 or 25% whole oats for calves up to approximately 12 wk old. Study 3 evaluated pelleted starters containing 0 or 62.75% soyhulls for calves up to approximately 8 wk old. Study 4 evaluated textured starters containing 0, 14, 28, and 42% soyhulls for calves between approximately 8 and 12 wk old. Calves were housed in individual pens in an unheated nursery with curtain sides through 8 wk and then in group pens of 6 calves/pen from 8 to 12 wk. Calves were bedded with straw. In study 1, calves fed the starters with extra molasses or sucrose had an average of 9% slower average daily gain (ADG) and greater average fecal scores from 42 to 56 d and 9% slower ADG from 0 to 56 d than calves fed the textured starter with low molasses. In study 2, ADG and feed efficiency (kg of feed/kg of gain) were 22 and 20% less, respectively, in calves fed the starter without oats from 0 to 28 d, but there were no differences thereafter. In study 3, calves fed starters with soyhulls had a 10% slower ADG and 8% lower efficiency of gain from 28 to 56 d than calves fed the starters without soyhulls. In study 4, ADG declined linearly as soyhulls increased in the starter. The change in ADG was 14% from 0 to 42% soyhulls. Replacing corn in a starter with molasses, sucrose, or soyhulls reduced postweaning ADG and increased the cost of ADG. Whole oats were an acceptable substitute for corn.     

The Australian brushtail possum (Trichosurus vulpecula) gonadotrophin alpha-subunit: analysis of cDNA sequence and pattern of expression

Substantial evidence has accumulated to suggest that in the near future implementation of the veto-cell-suppressor concept in the treatment of kidney allograft recipients might lead to the establishment of life-long specific allograft tolerance in the absence of further immunosuppressive therapy. Veto suppression prevents the generation of antigen-specific T-helper and cytotoxic T lymphocytes in vitro provided that the T-lymphocyte precursors specifically recognize antigenic peptides associated with the major histocompatibility complex molecules class II and class I, respectively, expressed on the surface of the veto-active cell. Data from a large number of experimental and clinical studies strongly indicate that veto-active cells function in vivo and are capable of preventing allograft rejection. Thus, donor-cell-mediated veto activity is the most likely explanation for the well-known graft tolerizing effect of pretransplant donor blood transfusions in kidney graft recipients. A prerequisite for a veto-active environment in vivo is the establishment of lymphoid microchimerism, in which veto-active donor and recipient cells mutually downregulate potential alloaggression.     

Intracellular localisation of urea-cycle enzymes in liver (author's transl)

Enzymes of the Krebs-Henseleit urea-cycle were localized by means of differential centrifugation and fractional tissue extraction in rat liver and in human liver. Argininosuccinatlyase (ASAL) and Argininosuccinatsynthetase (ASAS) represent enzymes of the soluble cytoplasmic fraction. Ornithine-ketoacid-transaminase(OKT), carbamyl-phosphate-synthetase (CPS) and ornithine-carbamyl-transferase (OCT) are localized in the mitochondrial and nuclei fractions of the liver cell. Most of the arginase activity is bound to subcellular structures (probably to nuclei). A small portion of arginase-activity was found in the soluble cytoplasmatic fraction. The enzymes of the Krebs-Henseleit urea-cycle are equally distributed in rat liver and in human liver. Differences in the subcellular localisation of (mitochondrial) enzymes in human liver could be attributed to mitochondrial breakage during tissue preparation and do not represent in-vivo conditions.     

Metabolomic Evidence for Peroxisomal Dysfunction in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome

Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a chronic and debilitating disease characterized by unexplained physical fatigue, cognitive and sensory dysfunction, sleeping disturbances, orthostatic intolerance, and gastrointestinal problems. People with ME/CFS often report a prodrome consistent with infections. Using regression, Bayesian and enrichment analyses, we conducted targeted and untargeted metabolomic analysis of plasma from 106 ME/CFS cases and 91 frequency-matched healthy controls. Subjects in the ME/CFS group had significantly decreased levels of plasmalogens and phospholipid ethers (p < 0.001), phosphatidylcholines (p < 0.001) and sphingomyelins (p < 0.001), and elevated levels of dicarboxylic acids (p = 0.013). Using machine learning algorithms, we were able to differentiate ME/CFS or subgroups of ME/CFS from controls with area under the receiver operating characteristic curve (AUC) values up to 0.873. Our findings provide the first metabolomic evidence of peroxisomal dysfunction, and are consistent with dysregulation of lipid remodeling and the tricarboxylic acid cycle. These findings, if validated in other cohorts, could provide new insights into the pathogenesis of ME/CFS and highlight the potential use of the plasma metabolome as a source of biomarkers for the disease.