Substrate Profiling of Anion Methyltransferases for Promiscuous Synthesis of S-Adenosylmethionine Analogs from Haloalkanes

Biocatalytic alkylation reactions can be performed with high chemo-, regio- and stereoselectivity using S-adenosyl-l -methionine (SAM)-dependent methyltransferases (MTs) and SAM analogs. Currently, however, this methodology is limited in application due to the rather laborious protocols to access SAM analogs. It has recently been shown that halide methyltransferases (HMTs) enable synthesis and recycling of SAM analogs with readily available haloalkanes as starting material. Here we expand this work by using substrate profiling of the anion MT enzyme family to explore promiscuous SAM analog synthesis. Our study shows that anion MTs are in general very promiscuous with respect to the alkyl chain as well as the halide leaving group. Substrate profiling further suggests that promiscuous anion MTs cluster in sequence space. Next to iodoalkanes, cheaper, less toxic, and more available bromoalkanes have been converted and several haloalkanes bearing short alkyl groups, alkyl rings, and functional groups such as alkene, alkyne and aromatic moieties are accepted as substrates. Further, we applied the SAM analogs as electrophiles in enzyme-catalyzed regioselective pyrazole allylation with 3-bromopropene as starting material.     

Effect of Pretreatment on Carbon-Supported Au/TiO2 Catalysts for Preferential Oxidation of CO

The impact of thermal treatment at various preparation stages of carbon supported Au/TiO₂ catalysts prior to oxidation of CO in the presence and absence of hydrogen was studied. An increase in catalytic activity for thermally treated samples due to a more ordered structure of TiO₂ was observed. A reversible deactivation of the catalysts occurred in the absence of hydrogen. However, the activity was restored at preferential CO oxidation conditions in presence of hydrogen.     

Porometry, porosimetry, image analysis and void network modelling in the study of the pore-level properties of filters

We present fundamental and quantitative comparisons between the techniques of porometry (or flow permporometry), porosimetry, image analysis and void network modelling for seven types of filter, chosen to encompass the range of simple to complex void structure. They were metal, cellulose and glass fibre macro- and meso-porous filters of various types. The comparisons allow a general re-appraisal of the limitations of each technique for measuring void structures. Porometry is shown to give unrealistically narrow void size distributions, but the correct filtration characteristic when calibrated. Shielded mercury porosimetry can give the quaternary (sample-level anisotropic) characteristics of the void structure. The first derivative of a mercury porosimetry intrusion curve is shown to underestimate the large number of voids, but this error can be largely corrected by the use of a void network model. The model was also used to simulate the full filtration characteristic of each sample, which agreed with the manufacturer's filtration ratings. The model was validated through its correct a priori simulation of absolute gas permeabilities for track etch, cellulose nitrate and sintered powder filters.     

Heterogeneously doped polyethylene glycol as nano-composite soft matter electrolyte

We have applied the concept of heterogeneous doping [1] to prepare and examine composite electrolytes, consisting of silica particles, low molecular weight polyethylene glycol solvents and lithium perchlorate salt. These “soggy sand” electrolytes combine high ionic conductivities (on the order of mS cm⁻¹) and high Li transference numbers (typically 60–80%) with improved mechanical properties. They were characterized using differential scanning calorimetry, dc-polarization and ac-impedance spectroscopy, zeta potential measurements and viscosimetry. Oxide, size and concentration as well as solvent molecular weight were varied to better understand the influence of ceramic oxide fillers on the ion conduction in these systems. As regarding the filler content, we observe that both conductivity and transference number of Li⁺ start increasing already at low volume fractions of oxide particles, reach a maximum and subsequently decrease to low values. The percolating network is – after initial partial coarsening – found to be stable within the time periods of the measurements.     

Entwicklung einer leistungsstarken Mikrorektifikationsapparatur für analytische und präparative Anwendungen

In this contribution it is reported about the realization of efficient micro rectification equipment (MRA), which can be operated intermittently or continuously and be used both for analytical as well as for preparative separations of mixtures of liquid substances. Different binary systems were separated. A theoretical separation stage number of 12 was obtained together with a height equivalent to one theoretical plate of 1.08 cm. Compared to the state of microtechnology this can be regarded as an excellent progress.     

NOX removal in excess oxygen by plasma-enhanced selective catalytic reduction

In the off-gases of internal combustion engines running with oxygen excess, non-thermal plasmas (NTPs) have an oxidative potential, which results in an effective conversion of NO to NO₂. In combination with appropriate catalysts and ammonia (NH₃-SCR) or hydrocarbons (HC-SCR) as a reducing agent, this can be utilized to reduce nitric oxides (NO and NO₂) synergistically to molecular nitrogen.

The combination of SCR and cold plasma enhanced the overall reaction rate and allowed an effective removal of NO_X at low temperatures. Using NH₃ as a reducing agent, NO_X was converted to N₂ on zeolites or NH₃-SCR catalysts like V₂O₅–WO₃/TiO₂ at temperatures as low as 100–200 °C. Significant synergetic effects of plasma and catalyst treatment were observed both for NH₃ stored by ion exchange on the zeolite and for continuous NH₃ supply.

Certain modifications of Al₂O₃ and ZrO₂ have been found to be effective as catalysts in the plasma-assisted HC-SCR in oxygen excess. With an energy supply of about 30 eV/NO-molecule, 500 ppm NO was reduced by more than half at a temperature of 300 °C and a space velocity of 20 000 h⁻¹ at the catalyst. The synergistic combinations of NTP and both NH₃- and HC-SCR have been verified under real diesel engine exhaust conditions.     

Crystallization of Polymer-Derived Silicon Carbonitride at 1873 K under Nitrogen Overpressure

The chemical stability of an amorphous silicon carbonitride ceramic, having the composition 0.57SiC·0.43Si₃N₄·0.49C is studied as a function of nitrogen overpressure at 1873 K. The ceramic suffers a weight loss at p _N2 < 3.5 bar (1 bar = 100 kPa), does not show a weight change from 3.5 to 11 bar, and gains weight above 11 bar. The structure of the ceramic changes with pressure: it is crystalline from 1 to 6 bar, amorphous at ∼10 bar, and is crystalline above ∼10 bar. The weight-loss transition, at 3.5 bar, is in excellent agreement with the prediction from thermodynamic analysis when the activities of carbon, SiC, and Si₃N₄ are set equal to those of the crystalline forms; this implies that the material crystallizes before decomposition. The amorphous to crystalline transition that occurs at ∼10 bar, and which is accompanied by weight gain, is likely to have taken place by a different mechanism. A nucleation and growth reaction with the atmospheric nitrogen is proposed as the likely mechanism. The supersaturation required to nucleate α-Si₃N₄ crystals is calculated to be 30 kJ/mol.     

Thermal Stability, Phase Evolution, and Crystallization in Si-B-C-N Ceramics Derived from a Polyborosilazane Precursor

Amorphous Si-B-C-N ceramic powder samples obtained by thermolysis of boron-modified polysilazane, {B[C₂H₄Si(H)NH]₃} _n , were isothermally annealed at different temperatures (1400–1800°C) and hold times (3, 10, 30, and 100 h). A qualitative and semiquantitative analysis of the crystallization behavior of the materials was performed using X-ray diffraction (XRD). The phase evolution was additionally followed by ¹¹B and ²⁹Si MAS NMR as well as by FT-IR spectroscopy in transmission and diffuse reflection (DRIFTS) modes. Bulk chemical analyses of selected samples were performed to determine changes in the chemistry/phase composition of the materials. It was observed that silicon carbide is the first phase to nucleate around 1400–1500°C, whereas silicon nitride nucleates at and above 1700°C. Crystallization accelerates with increasing annealing temperature and proceeds with increasing annealing time. Furthermore, the surface area of the powders strongly influences the thermal stability of silicon nitride and thus controls overall chemical and phase composition of the materials on thermal treatment.     

Real-Time Monitoring of (E)-β-Farnesene Emission in Colonies of the Pea Aphid, Acyrthosiphon pisum, Under Lacewing and Ladybird Predation

Aphids (Homoptera) are constantly under attack by a variety of predators and parasitoids. Upon attack, most aphids release alarm pheromone that induces escape behavior in other colony members, such as dropping off the host plant. In the pea aphid, Acyrthosiphon pisum Harris (Aphididae), the only component of this alarm pheromone is the sesquiterpene (E)-β-farnesene (EBF). EBF is thought to act as a kairomone by attracting various species of parasitoids and predators including lacewings and ladybirds. Lately, it also was proposed that EBF is constantly emitted in low quantities and used by aphids as a social cue. No study has focused on emission dynamics of this compound over a long time period. Here, we present the first long-time monitoring of EBF emission in aphid colonies using real-time monitoring. We used a zNose^TM to analyze the headspace of colonies of the pea aphid, under lacewing (Neuroptera: Chrysopidae) and ladybird (Coleoptera: Coccinellidae) predation, over 24 hr. We found no emission of EBF in the absence of predation. When either a ladybird adult or a lacewing larva was placed in an aphid colony, EBF was detected in the headspace of the colonies in the form of emission blocks; i.e., periods in which EBF was emitted alternating with periods without EBF emission. The number of emission blocks correlated well with the number of predation events that were determined at the end of each experiment. There was no circadian rhythm in alarm pheromone emission, and both predators were active during both night and day. Our results show that alarm pheromone emission pattern within an aphid colony is driven by the feeding behavior of a predator.