3S技术在江汉平原湿地监测中的应用

文章以江汉平原湿地监测为例，就3S技术在湿地监测中的应用做了说明。文章在简述江汉平原自然地理概况、江汉平原湿地3S技术监测意义的基础上，分析了进行湿地3S监测的技术方法与流程路线，建立了相应的湿地类型解译标志，并就湿地监测过程中的一些技术问题进行了讨论。     

基于S3C2416的公交电子站牌系统设计

为了提高城市公交的运营效率和服务质量,让乘客及时了解公交车实时车况,设计了一种基于S3C2416微处理器的新型公交电子站牌系统,并对该系统的组成、工作原理、关键技术及主要模块的软硬件设计进行了详细的阐述.系统以ARM为嵌入式硬件平台,采用当前先进的嵌入式技术和GPRS无线网络通信技术,实现了车辆到站预报、车辆到站提示、公交站点查询、公交车次查询等功能.测试结果表明,该系统性能良好、实时性强、稳定性高,具有巨大的市场价值.     

基于S3C2410构建PDA数据采集节点系统

描述了以现代的无损检测技术为基础,以S3C2410为核心构建的PDA数据采集系统。该系统实现了无线网络节点的数据采集功能。在此基础上设计了一套PDA数据采集,其硬件结构由S3C2410、无线网络节点和通信模块等组成;系统软件分为驱动程序模块、通信协议模块等,可应用于高校的教室温度采集系统。     

S → N acetyl migration in yeast glyceraldehyde-3-phosphate dehydrogenase

Zusammenfassung Nachweis, dass bei der Hefe-GAPD-katalysierten PNPA-Hydrolyse das als Zwischenprodukt gebildete S-Acetyl-Enzym durch eine intramolekulare Wanderung zu einem N-Acetyl-Derivat führen kann. Im Gegensatz zu dem aus Muskel isolierten Enzym findet im Hefe-Enzym eine Acetylwanderung bzw. eine Acetylierung des gegebenen Lysin statt, ohne wesentliche Beeinflussung durch das Coenzym (NAD).     

(S)-3-p-Methoxyphenyl-3-acetylaminopropan-1-ol, a New Metabolite of an Actinomycete.

(S)-3-p-methoxyphenyl-3-acetamidopropan-1-ol was isolated from cultures of an actinomycete (Streptomyces michiganensis). Its structural determination by spectroscopic means and its synthesis are described.     

论土地资源持续利用与"3S"系统的动态调控

土地资源持续利用是人口,环境与社会经济协调发展的前提和条件,中国必须按照国情制定相应的土地资源可持续发展战略;土地持续利用的目标,实现途径和指标体系在不崭家,地区和领域之间存在一害差异,但都必须考虑人口,资源,环境与发展各方面的影响因素;“３Ｓ”系统是遥感,地理信息系统与全球定位系统一体化集成的技术系统,具有对资源环境动态监测和综合功能,将成为２１世纪土地资源持续利用与管理新技术手段。     

Effects of araC and aphidicolin on DNA chain elongation rate in HeLa S3 cells

Summary The effects of araC and aphidicolin on DNA chain elongation rate were tested. The rate was markedly reduced at low concentrations. Total DNA synthesis was more inhibited, indicating a role of DNA polymerasea in replicon initiation.     

Effects of araC and aphidicolin on DNA chain elongation rate in HeLa S3 cells

The effects of araC and aphidicolin on DNA chain elongation rate were tested. The rate was markedly reduced at low concentrations. Total DNA synthesis was more inhibited, indicating a role of DNA polymerase a in replicon initiation.     

Alkaline phosphatase activity in relation to DNA synthesis in synchronized hela S3 cells

Zusammenfassung In synchronisierten HeLa S3-Zellen wurde die Aktivität der alkalischen Phosphatase in Bezug auf den Zellteilungszyklus untersucht. Die geringste Aktivität wurde während der S-Phase und die höchste beim Minimum der DNS-Syntheseaktivität festgestellt, und es wird angenommen, dass die alkalische Phosphatase als Transphosphorylase zur Regulation der Polgrösse von Nucleotiden dient.

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Acknowledgment. This research was supported in part by a grant from the Israel Cancer Association.     

The insulin-degrading enzyme is an allosteric modulator of the 20S proteasome and a potential competitor of the 19S

The interaction of insulin-degrading enzyme (IDE) with the main intracellular proteasome assemblies (i.e, 30S, 26S and 20S) was analyzed by enzymatic activity, mass spectrometry and native gel electrophoresis. IDE was mainly detected in association with assemblies with at least one free 20S end and biochemical investigations suggest that IDE competes with the 19S in vitro. IDE directly binds the 20S and affects its proteolytic activities in a bimodal fashion, very similar in human and yeast 20S, inhibiting at (IDE)?≤?30 nM and activating at (IDE)?≥?30 nM. Only an activating effect is observed in a yeast mutant locked in the “open” conformation (i.e., the α-3ΔN 20S), envisaging a possible role of IDE as modulator of the 20S “open”–”closed” allosteric equilibrium. Protein–protein docking in silico proposes that the interaction between IDE and the 20S could involve the C-term helix of the 20S α-3 subunit which regulates the gate opening of the 20S.     

Structure and assembly of the 20S proteasome

The barrel-shaped 20S proteasome is one of the two components of a larger 26S particle, the multicatalytic 2000-kDa protease complex. The proteolytic sites are located in the inner chamber of the 20S particle and are only accessible via narrow entrances. This paper reviews the current knowledge concerning proteasome formation, proteolytic activities, structural aspects and assembly. Eukaryotic proteasomes are made up by four rings each of which contains seven different subunits occurring at fixed positions. While the outer rings contain α-type subunits, the inner ones comprise β-type subunits. The current assembly model for eukaryotic 20S proteasomes is based upon the detection of 13S and 16S intermediates, respectively, in addition to previous findings with archaebacterial and eubacterial proteasome assembly. The available data suggest a cooperative assembly of the α-type and β-type subunits into half proteasome-like complexes followed by dimerization into proteasomes. During or after dimerization of half proteasomes, the β-type subunits are processed. The prosequence of the β-type subunits is essential for the assembly process and prevents protease activity of immature proteasomes.     

(S)-(+)-4,4,4-Trifluoro-3-(indole-3-)butyric acid,a novel fluorinated plant growth regulator

Racemic 4,4,4-trifluoro-3-(indole-3-)butyric acid (TFIBA) has been synthesized and shown to inhibitAvena coleoptile elongation. (S)-(+)-TFIBA (fig. 1), which was prepared by an enzymatic method and markedly promotes root growth of Chinese cabbage, lettuce and rice plants, is a novel fluorinated plant growth regulator. Activity of the (S)-(+)-enantiomer of TFIBA was 10-fold greater than that of the (R)-(–)-enantiomer in the first two plant species and 5-fold greater in rice.