Fungal Epithiodiketopiperazines Carrying α,β-Polysulfide Bridges from Penicillium steckii YE,and Their Chemical Interconversion

Some fungal epithiodiketopiperazine alkaloids display α,β-polysulfide bridges alongside diverse structural variations. However, the logic of their chemical diversity has rarely been explored. Here, we report the identification of three new ( 2 , 3 , 8 ) and five known ( 1 , 4 – 7 ) epithiodiketopiperazines of this subtype from a marine-derived Penicillium sp. The structure elucidation was supported by multiple spectroscopic analyses. Importantly, we observed multiple nonenzymatic interconversions of these analogues in aqueous solutions and organic solvents. Furthermore, the same biosynthetic origin of these compounds was supported by one mined gene cluster. The dominant analogue ( 1 ) demonstrated selective cytotoxicity to androgen-sensitive prostate cancer cells and HIF-depleted colorectal cells and mild antiaging activities, linking the bioactivity to oxidative stress. These results provide crucial insight into the formation of fungal epithiodiketopiperazines through chemical interconversions.     

Overview of the Therapeutic Potential of Aptamers Targeting Coagulation Factors

Aptamers are single-stranded DNA or RNA sequences that bind target molecules with high specificity and affinity. Aptamers exhibit several notable advantages over protein-based therapeutics. Aptamers are non-immunogenic, easier to synthesize and modify, and can bind targets with greater affinity. Due to these benefits, aptamers are considered a promising therapeutic candidate to treat various conditions, including hematological disorders and cancer. An active area of research involves developing aptamers to target blood coagulation factors. These aptamers have the potential to treat cardiovascular diseases, blood disorders, and cancers. Although no aptamers targeting blood coagulation factors have been approved for clinical use, several aptamers have been evaluated in clinical trials and many more have demonstrated encouraging preclinical results. This review summarized our knowledge of the aptamers targeting proteins involved in coagulation, anticoagulation, fibrinolysis, their extensive applications as therapeutics and diagnostics tools, and the challenges they face for advancing to clinical use.     

Proteomics Complementation of the Rat Uterotrophic Assay for Estrogenic Endocrine Disruptors: A Roadmap of Advancing High Resolution Mass Spectrometry-Based Shotgun Survey to Targeted Biomarker Quantifications

The widely used rat uterotrophic assay to assess known and potential estrogenic compounds only considers uterine weight gain as endpoint measurement. To complement this method with an advanced technology that reveals molecular targets, we analyzed changes in protein expression using label-free quantitative proteomics by nanoflow liquid chromatography coupled with high-resolution mass spectrometry and tandem mass spectrometry from uterine protein extracts of ovariectomized rats after daily 17β-estradiol exposure for five days in comparison with those of vehicle-treated control animals. Our discovery-driven study revealed 165 uterine proteins significantly regulated by estrogen treatment and mapped by pathway analyses. Estrogen-regulated proteins represented cell death, survival and development, cellular growth and proliferation, and protein synthesis as top molecular and cellular functions, and a network found with the presence of nuclear estrogen receptor(s) as a prominent molecular node confirmed the relevance of our findings to hormone-associated events. An exploratory application of targeted proteomics to bisphenol A as a well-known example of an estrogenic endocrine disruptor is also presented. Overall, the results of this study have demonstrated the power of combining untargeted and targeted quantitative proteomic strategies to identify and verify candidate molecular markers for the evaluation of endocrine-disrupting chemicals to complement a conventional bioassay.     

The relative influences of Al2O3 and Fe2O3 on the chemical durability of silicate glasses at different pH values

The influence of the pH of aqueous solutions on the chemical durability of two glasses in the system Na₂O-FeO-Fe₂O₃-SiO₂ has been compared with that of two glasses in the system Na₂O-MgO-Al₂O₃-SiO₂ where equimolar substitution of MgO for FeO and Al₂O₃ for Fe₂O₃ have been made. The presence of Fe₂O₃, and particularly of Al₂O₃, in glass reduces its alkali extraction in the pH range 4 to 9. The extraction results have been discussed and interpreted in the light of the available standard thermochemical data for the component oxides of these glasses.     

Effects of THF as cosolvent in the preparation of polydimethylsiloxane/polyethersulfone membrane for gas separation

Polydimethylsiloxane/polyethersulfone (PDMS/PES) asymmetric membranes are widely applied in gas separation. However, the effects of common cosolvent on these membranes remain unknown. In order to study the changes in membrane morphology and gas separation properties, asymmetric PDMS/PES membranes were prepared. The studied parameters were types of cosolvents, tetrahydrofuran (THF) concentration, evaporation time, and PDMS concentration. Membrane morphology was examined using scanning electron microscopy and gas separation was conducted using pure CO₂, N₂, CH₄, and Hat 25°C. The addition of cosolvent into the polymer solution decreased the dope viscosity and delayed liquid–liquid demixing during phase inversion. Macrovoids formation was observed in substructure layer after adding THF and these macrovoids elongated with the reduction in THF content. There were microvoids formed on top of macrovoids and microvoids layer became thicker due to the increasing evaporation time of solvents before coagulation in nonsolvent. The PDMS coating on the PES membrane formed a dense skin layer and exhibited higher selectivity compared to the uncoated membrane. Membrane contained THF cosolvent with 60 s evaporation time and 3 wt% coated PDMS is the optimum membrane among other membranes in this work. The CO₂/N₂ selectivity was enhanced by 73.3% with CO₂ permeance of 44.86 GPU. POLYM. ENG. SCI., 54:2177–2186, 2014. © 2013 Society of Plastics Engineers     

Modification and characterization of photo-cured sodium alginate film with ethylene glycol: effect of additives

Thin films of sodium alginate (SA) were prepared by casting from methanol solutions. Tensile strength and elongation at break (Eb%) of the films were found to be 20.4 MPa and 11.6 %, respectively. A series of SA solutions (formulations) were prepared by blending varying percentages (2–8 % by wt) of ethylene glycol (EG) and then films were prepared and cured under UV radiation at different intensities (5–35 UV passes). Monomer concentration, soaking time, and radiation dose were optimized in terms of polymer loading and mechanical properties of the cured films. For the improvement of the properties, several acrylic monomers of different functionalities as additives (2 %) like 2-ethylhexyl acrylate, 1,4-butanediol diacrylate, and trimethylolpropane triacrylate were incorporated with EG with the aid of UV radiation. Further analyses of the prepared films were characterized by FTIR and thermogravimetric analysis. Water uptake behavior was determined for the raw and cured SA films.     

Preparation and characterization of phosphoric acid composite membrane by radiation induced grafting of 4‐vinylpyridine onto poly(ethylene‐co‐tetrafluoroethylene) followed by phosphoric acid doping

Preparation of phosphoric acid composite membranes by radiation induced grafting of 4‐vinylpyridine (4‐VP) onto electron beam irradiated poly(ethylene‐co‐tetrafluoroethylene) film followed by phosphoric acid doping was investigated. The effect of grafting parameters (monomer concentration, absorbed dose, reaction time, and temperature) on the degree of grafting (G%) in the membrane precursor and its relation with the amount of acid doped was studied. The proton conductivity of the obtained membranes was evaluated in correlation with G% and temperature using ac impedance. Fourier transform infrared, thermal gravimetric analysis, X‐ray diffraction, and universal mechanical tester were used to investigate chemical composition, thermal resistance, structure, and mechanical properties of the membranes, respectively. The membranes of 34 and 49% recorded high proton conductivity in the magnitude of 10^‐2 S cm^‐1 without humidification. The membranes were also found to have reasonable mechanical integrity together with thermal stability up to 160°C. The obtained membranes are suggested to be less‐water dependent and have potential for testing in high temperature polymer electrolyte membrane fuel cell. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Effect of Anhydride Modification on the Thermal Stability of Cultivated Acacia mangium

Abstract

This paper tests the hypothesis that propionic and succinic anhydride modification will improve the thermal stability of cultivated Acacia mangium wood. The thermal stability of modified wood was characterized with thermogravimetric analysis. Evidence of modification was confirmed by Fourier transform infrared analysis. Our results show that chemical modification with anhydrides improves the thermal stability of the Acacia wood. The higher thermal stability of anhydride-modified Acacia wood compared with unmodified wood is attributed to the reduction in hydrophilic nature of the wood due to esterification. Succinylated wood has better thermal stability than propionylated wood based on the values of on-set degradation temperatures, the temperatures at which 30, 50, and 70% degradation occurred, and the activation energy. The improved thermal stability of modified wood compared with the unmodified wood will offer potential for better utilization of Acacia mangium.