Fortschritte in der analytischen Chemie seltener Metalle

Ohne Zusammenfassung     

Digital simulation as an aid to sample scheduling in a routine laboratory for liquid chromatography

A computer model is described to aid decision-making in a routine laboratory for liquid chromatography. The managerial demand was to reduce the delay times of the samples in the laboratory despite an increasing sample input. Knowledge derived from records on the laboratory and from the experience of the laboratory staff is used to develop a simulation model of the laboratory. The model is applied to study the effects of several factors on the performance of the laboratory in order to trace the bottlenecks.     

The pH-static enzyme sensor : An ISFET-based enzyme sensor,insensitive to the buffer capacity of the sample

An ISFET-based urea sensor is combined with a noble-metal electrode which provides continuous coulometric titration of the products of the enzymatic reaction. The sensor thus becomes independent of the buffer capacity of the sample; and because the enzyme is operating at a constant pH, the linear response range is expanded.     

Surface characterization of a cross‐linked cytochrome c film on cysteamine‐modified gold electrodes

The aim of the present paper is to characterize a cross‐linked horse heart cytochrome c (HHC) film on cysteamine‐modified gold electrodes. The HHC film was deposited using 1‐ethyl‐3‐(3‐dimethylaminopropyl)‐carbodiimide (EDC) as a coupling agent. Attenuated total reflection infrared (ATR‐IR) spectroscopic analyses were performed to characterize the newly formed surface on a qualitative and conformational level. The film thickness was measured using a noncontact optical surface profiler, while quantitative data and information on the heterogeneity of the film were obtained by means of synchrotron radiation X‐ray micro fluorescence (SR micro‐XRF). Results indicate that, in addition to electrochemical studies, spectroscopic analysis methods are essential to gain insight in the effect of immobilization strategies on protein conformations. The latter is of relevance in the development and optimization of biosensors. Copyright © 2009 John Wiley & Sons, Ltd.     

设计和仿真无线局域网设备天线

对带有开关电路的2.4 GHz极化分集印刷天线进行电磁场及电磁场与电路协同仿真 通过采用极化分集技术,可以用低成本PCB基片制造具有良好接收机性能的无线局域网设备(WLAN)天线.本文将描述如何使用最新的三维电磁场(EM)仿真工具来设计和仿真一对2.4GHz正交极化的印刷偶极子天线,同时预测表面电流和相关的远场辐射图.     

Enantioselective route to 3-vinylidene tetrahydropyrans and 3-vinylidene oxepanes based on a silyl-Prins cyclization

A general method has been developed for the asymmetric synthesis of 3-vinylidene tetrahydropyrans and 3-vinylidene oxepanes based on the Lewis acid-catalyzed intramolecular reactions of oxocarbenium ions with propargylsilanes. The observed excellent diastereoselectivity and a high asymmetric induction offer a new synthetic method with a wide scope and generality.     

A transmission line model for arrays of rectangular microstrip antennas

A very efficient transmission line model for the analysis of arrays of rectangular microstrip antennas is presented. The structure of the model is discussed, and its validity is proved. This is done for the isolated microstrip antenna as well as for the coupling between antennas. Then follows a discussion of the numerical efficiency. And finally a numerical example shows the effect of mutual coupling on the impedance and radiation pattern of a 21 element Chebyshev array at different scanangles.     

The kalimantacin/batumin biosynthesis operon encodes a self-resistance isoform of the FabI bacterial target

BatG is a trans-2-enoyl-ACP reductase, encoded in?the kalimantacin/batumin (kal/bat) biosynthesis operon. It is not essential for the production of the kal/bat secondary metabolite. Instead, BatG is an isoform of FabI, conferring full resistance to target bacteria. It also complements FabI in its role in fatty acid biosynthesis. The identification of FabI as the antibacterial target is important to assess clinical potential of the kalimantacin/batumin antibiotics against Staphylococcus aureus.     

Identification of poliovirions and subviral particles by capillary electrophoresis

Poliovirions, purified from infected cell extracts with anion-exchange chromatography, can be analyzed and identified by CE in untreated fused silica capillaries using UV detection. Other subviral particles can be eluted as well from the same infected cell extract using a higher salt concentration buffer on the ion-exchange chromatography. Virions can be identified because of their conversion into empty capsids upon heating at 56°C. As a result of heating, the viral genome is released from the capsid. Here, we show that during this incubation some intermediate particles were found. The latter were identified by enzymatic peak shift analysis. The high salt concentration eluate subviral particles were analyzed with preincubation affinity CE together with their sensitivity for RNase and proteinase K treatment. Electropherograms of the higher salt concentration eluate display a mixture of at least four different subviral particles. One particle proved to have an [N1, H] antigenicity and was resistant to RNase and proteinase K digestion. The remaining particles were all sensitive to proteinase K treatment. This CE method proved to be valuable in the detection, identification and analysis of poliovirions and poliovirus particles offering an alternative powerful, cheap, fast and easy analysis method.