Aqueous poly(urethane–urea) dispersions and cast films based on m‐TMXDL. 1. Structure–property relationships

Aqueous poly(urethane–urea) dispersions were prepared from polycaprolactone diol, α,α,α′,α′‐tetramethyl‐1,3‐xylylene diisocyanate (m‐TMXDI) and α,α‐dimethylol propionic acid (DMPA) using a prepolymer mixing process. In the process, polyurethane prepolymers were neutralised with triethylamine and the chains extended in water with either hydrazine, 1,2‐ethylene diamine or 1,2‐propylene diamine. For comparison, some samples were prepared from a more commonly used diisocyanate, isophorone diisocyanate (IPDI). Dispersion characteristics and basic structure–property relationships of the cast films were determined. m‐TMXDI provided some advantages over IPDI in the preparations since its use gave lower prepolymer viscosities and better resistance to elevated temperatures. Films prepared from m‐TMXDI dispersions exhibited considerably lower values of Young's modulus and hardness and higher elongations at break than those prepared from IPDI‐based dispersions for analogous compositions, whereas differences in the average particle sizes or viscosities of the dispersions were only small. When the DMA content was varied, the dispersions and cast films of m‐TMXDI‐based systems showed similar changes as are known to occur in IPDI‐based systems: as the DMPA content was increased, the average particle size of the dispersions decreased and the viscosity increased, and for the cast films, the Young's modulus and tensile strength increased and the maximum elongation at break decreased. Changing the chain‐extension agent from hydrazine to 1,2‐ethylene diamine, to 1,2‐propylene diamine and had little effect on the particle size of the dispersions, but increased the Young's modulus and hardness of the respective cast films. Molar masses of the chain‐extended polymers were unexpectedly low. DSC analysis of cast films indicated that the degree of crystallisation of the soft or hard domains was low. © 2002 Society of Chemical Industry     

Blends of natural rubber and polyurethane latices studied by 1H wideline and 13C MAS solid‐state NMR

¹H wideline and ¹³C magic‐angle spinning NMR have been used to study the morphology and dynamics of latex‐cast and solution‐cast film blends of natural rubber (NR) and a polyurethane (PU) based on poly(?‐caprolactone) diol and isophorone di‐isocyanate. ¹H T₁ and T_1ρ relaxation times have been measured, and the extent of interpenetration of the NR and PU constituents has been monitored using the Goldman–Shen technique. The NMR spectra and relaxation properties indicated that the NR and PI constituents largely occupy separated domains on a distance scale of >10 nm. The Goldman–Shen experiments indicated that there was slightly greater contact between NR and PU in the solution‐cast samples than in the latex‐cast. The tensile properties of the films have been measured. The tensile strength and initial Young's modulus pass through a maximum at a PU content of about 50 wt%. © 2002 Society of Chemical Industry     

Stepwise optimisation of enzyme production in solid state fermentation of waste bread pieces

When it is not consumed, bread presents a major source of food waste, both in terms of the amount and its economic value. However, bread also possesses the characteristics of an ideal substrate for solid state fermentation. Yet nearly all wasted bread ends up in landfill sites, where it is converted into methane by anaerobic digestion. Governments are finally taking action and, according to the EU Landfill Directive, for example, biodegradable municipal waste disposed into landfills must be decreased to 35% of 1995 levels, by 2020. Solid state fermentation of waste bread for the production of value added products is a novel idea, which could help with the achievement of this target. In this study, glucoamylase and protease production from waste bread pieces, via solid state fermentation, was investigated in detail. The optimum fermentation conditions for enzyme production were evaluated as, 20 mm particle size, 1.8 (w/w, db) initial moisture ratio, and duration of 144 h. Under these conditions, glucoamylase and protease activities reached up to 114.0 and 83.2 U/g bread (db), respectively. This study confirms that waste bread could be successfully utilised as a primary raw material in cereal based biorefineries.     

Obesity: Prevalence,Theories, Medical Consequences,Management, and Research Directions

Obesity and its associated disorders are a growing epidemic across the world. Many genetic, physiological, and behavioral factors play a role in the etiology of obesity. Diet and exercise are known to play a valuable role in the treatment and prevention of obesity and associated disorders such as hypertension, heart disease, and diabetes. Therefore, the purpose of this review is to examine the prevalence, etiology, consequences, and treatment of obesity.     

The effects of long‐term exposure of flax fiber reinforced polymer to salt solution at high temperature on tensile properties

Most research on natural fiber composites has been primarily conducted on randomly‐oriented fibers. This study is focused on the short‐ and long‐term performances of flax fiber‐reinforced polymer (Flax‐FRP) made from continuous unidirectional fiber mats, and compares it to Glass‐FRP composite. The study looked into the effect of number of layers on properties, comparing wet layup (WL) to vacuum bag (VB) molding, and aging in a 3.5% salt solution for up to 365 days at 23, 40, and 55°C. Results show that Flax‐FRP has a tensile strength and modulus of one third the values of Glass‐FRP. Using the VB process, Flax‐FRP showed a strength and modulus 18 and 36% higher, respectively, than WL specimens. As the number of layers increased from one to five, the strength and modulus also increased but stabilized at three layers. After 365 days of conditioning at 23, 40, and 55°C, WL specimens showed a strength retention of 81, 73, and 69%, respectively. Using the Arrhenius relationship, it was estimated that both WL and VB Flax‐FRP would retain 60% of their tensile strength after 100 years of saltwater exposure at an annual mean temperature of 10°C. POLYM. COMPOS., 37:3234–3244, 2016. © 2015 Society of Plastics Engineers     

CD26 Induces Colorectal Cancer Angiogenesis and Metastasis through CAV1/MMP1 Signaling

CD26 has been reported as a marker for colorectal cancer stem cells endowed with tumor-initiating properties and capable of colorectal cancer (CRC) metastasis. In this study, we investigated the functional effect of CD26 on CRC angiogenesis and metastasis, and the potential underlying mechanism. The functional effects of CD26 overexpression or repression were determined by a wound healing experiment, and cell migration and invasion assays in vitro and in mouse models. Differentially expressed genes regulated by CD26 were identified by genome-wide mRNA expression array and validated by quantitative PCR. CD26 functionally regulated CRC cell migration and invasion in vitro and angiogenesis and metastasis in vivo. Genome-wide mRNA expression array and qPCR showed that MMP1 was up-regulated in CD26+ subpopulation, and a subsequent experiment demonstrated the regulatory effect of CD26 on MMP1 in CRC cell lines with CD26 repression or overexpression. Furthermore, overexpression of CAV1 abrogated the CD26-regulated MMP1 induction in CRC cell lines. This study demonstrated the functional roles of CD26 in inducing CRC migration, invasion, angiogenesis and metastasis and identified the potential involvement of MMP1 and CAV1 in such process. CD26 is an attractive therapeutic target for combating tumor progression to improve the prognosis of CRC patients.     

Evidence for the mitochondrial biosynthesis of 3R-hydroxy-5Z,8Z,11Z,14Z-eicosatetraenoic acid in the yeast Dipodascopsis uninucleata

The biosynthesis of 3R-hydroxy-5Z,8Z,11Z,14Z-eicosatetraenoic acid (3R-HETE) from arachidonic acid (20∶4n−6) by the hyphal-forming yeast, Dipodascopsis uninucleata, in cell-free enzyme extracts required CoASH, ATP, NAD⁺ and Mg²⁺; 3R-HETE was present as the CoA derivative in enzyme extracts and its biosynthesis was associated with mitochondria. Its synthesis was high from arachidonoyl-CoA (15% conversion of the substrate; 22 nmol mg protein⁻¹·h), but significantly higher from trans-2-arachidonoyl-CoA (53 nmol mg protein⁻¹·min). Aspirin, an inhibitor of prostaglandin endoperoxide synthase synthase (cyclooxygenase), did not significantly inhibit 3R-HETE biosynthesis in enzyme extracts, as opposed to antimycin A (46% inhibition). The chirality of 3-HETE was 95% R and 5% S. 3R-HETE has the same chirality as the products of peroxisomal enoyl-CoA hydratases of Neurospora crassa and Saccharomyces cerevisiae; the difference appears to be that in D. uninucleata the R-enantiomers are synthesized in mitochondria. Exogenously supplied eicosapentaenoic acid was converted to 3-hydroxy 5Z,11Z,14Z,17Z-eicosapentaenoic acid by cell-free enzyme extracts though there was no requirement for a 5Z,8Z-diene structure for the biosynthesis of 3-hydroxylated fatty acids as 3-hydroxy-8Z,11Z,14Z, and 3-hydroxy-11Z,14Z,17Z-eicosatrienoic acids were synthesized from the corresponding fatty acids. We found no evidence for the synthesis of the prostaglandins F_2α and F₂.     

Vascular Architecture Generates Fine Scale Variation in Systemic Induction of Proteinase Inhibitors in Tomato

Systemic induction following damage has been found in many plant species. Despite this widespread appreciation for the importance of induction, few studies have characterized the spatial variability of induction. We used tomato, Lycopersicon esculentum, to examine how damage to a single leaf affected the spatial distribution of systemic induction of proteinase inhibition in leaves above the damaged leaf. We crushed each leaflet of the second true leaf with forceps and measured the spatial distribution of proteinase inhibition in leaves 3, 4, and 5 at 8, 16, 24, 48, 72, and 120 hr. Constitutive levels of proteinase inhibitor activity were quantified in undamaged plants. We hypothesized that, due to vascular control of signal movement, systemic induction would show both among and within leaf variability. Following damage to leaf 2, induction was most pronounced in leaf 5 and minimal in leaf 3. In general, proteinase inhibitor activity was greatest at 24 hr and then declined. As predicted by vascular architecture, the near side of leaves in adjacent orthostichies showed higher induction than the far side of leaves. There was no increase in proteinase inhibitor activity in the undamaged neighboring plants. Overall our results demonstrate that systemic induction of proteinase inhibitors is partially controlled by vascular architecture and that future studies on systemic induction should examine the vascular architecture of the plants being studied. We argue that this spatial variation may influence the performance of herbivores sensitive to induced chemical changes.     

Responses of the Crab <Emphasis Type="Italic">Heterozius rotundifrons</Emphasis>to Heterospecific Chemical Alarm Cues: Phylogeny vs. Ecological Overlap

The big-handed brachyuran crab Heterozius rotundifronsextends the time spent in its anti-predator posture, limb extended posture, if exposed to chemical cues from crushed conspecifics. In this study, we tested whether crabs also respond to chemical cues from crushed heterospecific crabs, and if so, whether phylogenetic relations or ecological overlap is more important in influencing the duration of the anti-predator posture. Chemical cues from two other brachyuran crabs (Cyclograpsus lavauxi and Hemigrapsus sexdentatus), which do not overlap directly in ecological distribution with H. rotundifrons, elicited a duration of the anti-predator posture that was indistinguishable from that produced by conspecific chemical cues. In contrast, chemical cues from two anomuran crabs (Petrolisthes elongatus and Pagurus novizealandiae) that overlap in ecological distribution with H. rotundifrons, elicited durations of the antipredator posture that were significantly shorter than those of either conspecifics or more closely related crab species. Thus, phylogenetic relationship seems to be more important than ecological overlap in influencing anti-predator behavior in H. rotundifrons.     

Electro-Oxidation of Carbonate in Aqueous Solution on a Platinum Rotating Ring Disk Electrode

The kinetics of electro-oxidation of carbonate aqueous solution on a platinum electrode were examined by a rotating ring (platinum) – disk (platinum) electrode in aqueous sodium carbonate/bicarbonate solutions (25 °C, pH = 10.75) with the peroxide stabilizing additives sodium silicate, magnesium sulphate and sodium DTPA such as are used in brightening mechanical wood pulp. A theoretical model based on the experimental data is proposed to describe this electro-oxidation process. The model shows consistency between the experimental results and the expectation from the proposed reaction sequence. The first-order rate constants at 25 °C, pH = 10.75 in 1.13 M (Na₂CO₃ + NaHCO₃) for carbonate electro-oxidation to percarbonate (a.k.a. peroxidicarbonate C₂O₆^2-), percarbonate hydrolysis to hydrogen peroxide and hydrogen peroxide electro-oxidation to oxygen are estimated from the experimental data, respectively, as (1.43±0.1) × 10⁻¹¹cm s⁻¹ (extrapolated to the equilibrium electrode potential which is estimated as ca. 0.21 (vs SCE)), (1.1 ± 0.2) × 10⁻² s⁻¹ and (5.6±0.5) × 10⁻⁸cm s⁻¹ (extrapolated to the equilibrium electrode potential of −0.019 V (vs SCE)).