Substrate Scope for Human Histone Lysine Acetyltransferase KAT8

Biomedically important histone lysine acetyltransferase KAT8 catalyses the acetyl coenzyme A-dependent acetylation of lysine on histone and other proteins. Here, we explore the ability of human KAT8 to catalyse the acetylation of histone H4 peptides possessing lysine and its analogues at position 16 (H4K16). Our synthetic and enzymatic studies on chemically and structurally diverse lysine mimics demonstrate that KAT8 also has a capacity to acetylate selected lysine analogues that possess subtle changes on the side chain and main chain. Overall, this work highlights that KAT8 has a broader substrate scope beyond natural lysine, and contributes to the design of new chemical probes targeting KAT8 and other members of the histone lysine acetyltransferase (KAT) family.     

Altered Signal Transduction in the Immune Response to Influenza Virus and S. pneumoniae or S. aureus Co-Infections

Influenza virus is a well-known respiratory pathogen, which still leads to many severe pulmonary infections in the human population every year. Morbidity and mortality rates are further increased if virus infection coincides with co-infections or superinfections caused by bacteria such as Streptococcus pneumoniae (S. pneumoniae) and Staphylococcus aureus (S. aureus). This enhanced pathogenicity is due to complex interactions between the different pathogens and the host and its immune system and is mainly governed by altered intracellular signaling processes. In this review, we summarize the recent findings regarding the innate and adaptive immune responses during co-infection with influenza virus and S. pneumoniae or S. aureus, describing the signaling pathways involved and how these interactions influence disease outcomes.     

Catalytic degradation of waste high-density polyethylene into fuel products using BaCO3 as a catalyst

Waste high-density polyethylene (HDPE) was degraded thermally and catalytically using BaCO₃ as a catalyst under different conditions of temperature, cat/pol ratio and time. The oil collected at optimum conditions (450 °C, 0.1 cat/pol ratio and 2 h reaction time) was fractionated at different temperatures and fuel property of the fractions and parent oil was evaluated by their physicochemical parameters for fuel tests. The results were compared with the standard values for gasoline, kerosene and diesel oil. Boiling point distribution (BPD) curves were plotted from the gas chromatographic study of the samples and compared with that of the standard gasoline, kerosene and diesel. The oil samples were analyzed using GC/MS in order to find out their composition. The physical parameters and the composition of the parent oil and its fractions support the resemblance of the samples with the standard fuel oils. The light fractions best match with gasoline, the middle fractions match with kerosene and the heavier fractions match with diesel oil in almost all of the characteristic properties.     

A Thermodynamic Investigation of the Redox Properties of VPO Catalysts

Abstract  

The redox properties of a vanadium phosphorus oxide (VPO) catalyst with a V:P ratio of one were investigated using Coulometric Titration at 873 K. Equilibrium between (VO)₂P₂O₇ and VOPO₄ exists at a P(O₂) of 3 × 10⁻⁴ atm, corresponding to ΔG of −60 kJ/mol O₂. This value for VPO is significantly lower than that measured with other vanadium-containing catalysts that have been studied. Furthermore, compared to other vanadium catalysts, V⁺⁴ was stabilized against further reduction at lower P(O₂). These redox thermodynamics may help to explain the unique catalytic properties of VPO catalysts for partial oxidation of butane to maleic anhydride.     

Preparation and characterization of uniform molecularly imprinted polymer beads for separation of triazine herbicides

Uniform molecularly imprinted polymer beads were synthesized by precipitation polymerization for separation of triazine herbicides. A series of imprinted polymers were prepared using ametryn as template and divinylbenzene as crosslinking monomer, in combination with three different functional monomers under different solvent conditions. Under optimized reaction conditions, we obtained uniform molecularly imprinted polymer microspheres that display favorable molecular binding selectivity for triazine herbicides. The imprinted polymer beads synthesized using methacrylic acid as functional monomer in a mixture of methyl ethyl ketone and heptane showed the best results in terms of particle size distribution and molecular selectivity. Compared with nonimprinted polymer microspheres, the imprinted microspheres displayed significantly higher binding for a group of triazine herbicides including atrazine, simazine, propazine, ametryn, prometryn, and terbutryn. For the first time, precipitation polymerization has been used to produce highly uniform imprinted microspheres suitable for affinity separation of triazine herbicides. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

KnowVolution of a Fungal Laccase toward Alkaline pH

To date, commercial laccase preparations are used in the food, textile, and paper and pulp industries (mild pH). Laccases are attractive in the synthesis of dye molecules or oxidative lignin treatment, which take place at high pH (≥8.0). So far, one fungal laccase has been reported to be active at alkaline pH. Herein, engineering of the fungal laccase from Melanocarpus albomyces (MaL) for increased activity toward the substrate 2,6-dimethoxyphenol at pH (≥9.0) is reported. Through a knowledge-gaining directed evolution (KnowVolution) campaign, the key positions Leu365 and Leu513 were identified to increase alkaline tolerance. Both positions are located in close proximity of the T1Cu site. Molecular docking and simulations studies reveal that both substitutions act in a synergic way to stabilize and improve laccase activity at higher pH. Kinetic characterization of the final variant MaL-M1 (L365E/L513M) revealed at pH 9.8 a threefold improved k_cat (k_cat=(6.0±0.2) s⁻¹) compared with that of wild-type M. albomyces laccase (k_cat=(2.11±0.07) s⁻¹).     

Microstructure and Composition of Primary and Recycled Single Grains of YBCO,GdBCO‐Ag,and SmBCO‐Ag Bulk Superconductors

The widespread use of single grain RE‐Ba‐Cu‐O [(RE)BCO] bulk superconductors, where RE is typically Sm, Gd, or Y, is, in part, limited by the relatively high costs of precursor powders and the low success rate of the manufacturing process. Both these problems can be addressed by recycling primary‐processed grains in which the initial growth process has failed in some way. Key to the use of recycled grains in practical applications is an assurance that their properties and performance are not inferior to those of primary grown grains. In this work, we describe the differences between the growth process, microstructure, and properties of primary and recycled (RE)BCO single grains. We observe that the mechanism of growth is the same for both primary and recycled single grain samples in all three RE‐based systems investigated. In the recycling process additional liquid‐rich phase powder is provided beneath a failed sample, whereby this liquid phase infiltrates upwards and contributes a sufficient concentration of additional RE species at the growth front to enable samples to grow relatively easily in the form of single grains by producing a more uniform composition at the growth front, which leads directly to an increased tolerance to the presence of Ag and Ce‐rich agglomerates. Importantly, we observe that the recycled samples have a much more uniform composition, and therefore exhibit more uniform superconducting properties, than single grain samples fabricated by a primary grown process.