远程教育培训给生物教学带来新的生机

远程教育培训给生物教学带来新的生机。夯实了专业知识,梳理了生物知识,使我认识到应该如何把握生物课堂教学,提高了课堂教学设计能力,凝聚了生物教师的力量,使老师们学到了很多知识和教学技能,解决了平时教学中的一些难题,提升了生物的教学水平。     

越来越苍老的世界

中国全面推行计划生育政策,少生了3亿多人,节约了7万亿抚养费,也少了3亿可以负担养老的劳动力。由于老龄化加速,老年抚养比由1964年的6.4%上升为2002年的11.6%,离退休金平均实际递增18.9%。到2050年,中国的抚养比将可能达到70%。老龄化速度,法国用了115年,英国用了80年,美国用了60年,我国用了18年。     

酷想大晒台

哎呀呀,这个世界乱套了!大人变成了小孩,小孩变成了大人。现在,终于轮到各位小酷想家来当家做主了,快来看看他们都有什么出色的表现吧!看到爸妈变成了小孩,我立马学着他们的样子,下达了第一道命令:写作业去!我想他们一定会哭的,因为老师留的作业实在是太多了。新浪YOYO     

一年又一年

上了年纪的人都有相似的感觉,就是年纪越大,时间好像过得越快。小时候,过了元旦盼春节,过了春节盼五一、六一,过了六一盼国庆,过了国庆再盼元旦。时间总是那么漫长,盼望的假期似乎总是姗姗来迟。而如今,似乎一眨眼,一年就过去了。我给这个现象总结了一个理论,叫做相对     

亚热带丘陵茶园间作白三叶的土壤环境调控效果

在亚热带丘陵区1年生幼龄茶园通过连续4年间作白三叶大田试验,研究了其对茶园土壤环境及茶叶品质、产量的影响,结果表明,茶园间作白三叶降低了土壤容重,提高了土壤孔隙度、有机质、全氮、水解氮的含量及钾的活性,消耗了部分有效磷;增加了土壤关键层次（0～20cm）和关键时期（4～6月）的水分含量,延缓和缩短了夏季高温干旱与秋季持续干旱时间;获得了土壤降温时增温、保温与升温时降温的双向动态调控效果．增加了同一层次土壤温度的稳定性,延缓了高温和低温的出现时间,缩短了过度高温时间。从而促进了茶树生长,改善了茶叶品质,显著增加了茶叶产量。与清耕茶园相比,茶园间作白三叶后,春秋茶的酚氨比分别下降了17．10％和30．90％,产量提高了32.65％。     

促进微生物实验技术创新水平的改革初探

为了加强对本科生综合素质和能力的培养 ,激发学生的学习兴趣 ,我们对微生物实验课的教学内容进行了一系列改革 ,优化了实验项目 ,节约实验成本 ,并且引入科研成果转化实验 ,同时改进了实验方法和手段 ,实验结果更为准确。这些措施蕴含了较高的理论水平 ,增加了教学信息量 ,明显提高了教学效果 ,为培养高素质人才奠定了基础。     

电镀行业重金属在线回收清洁生产技术

为了提高电镀企业水重复利用率, 降低物料单耗, 减少重金属产生量, 提升企业清洁生产水平, 通过某电镀厂清洁生产实例, 介绍了膜分离和离子交换在线回收技术的基本原理和技术特性, 计算了经济可行性, 对比了水重复利用率、物料单耗、重金属产生量三项指标。结果表明, 该技术的内部收益率大于基准收益率, 镀镍工序水重复利用率提高了60.1%, 物料单耗降低了4.51%, 废水中镍产生量每年减少360 kg, 镀铬工序水重复利用率提高了46.0%, 物料单耗降低了10.4%, 废水中Cr(VI)产生量每年减少340 kg。     

具有分布时滞传染病模型的渐近分析

本文讨论了具有一般分布函数（核）的微分方程传染病模型,给出了平衡点,讨论了稳定性,得到了阈值定理．     

砷对烤烟(Nicotiana tabacum L.)碳代谢的影响

采用盆栽试验,系统地研究了砷对烤烟全生育期碳代谢及其过程的影响,结果表明,砷降低了烤烟整个生育期的叶绿素含量、光合速率、蔗糖合成酶（SS,合成方向）活性和现蕾以后的蔗糖磷酸合成酶（SPS）活性,提高了全生育期的SS（分解方向）活性和可溶性糖含量,因而抑制了碳的同化和蔗糖的合成,促进了蔗糖的分解,不利于碳向积累方向转化。砷提高了全生育期的腺苷二磷酸葡萄糖焦磷酸化酶（ADPG-PPase）活性,增加了团棵期和现蕾期淀粉的积累,降低了团棵期和采收期的可溶性淀粉酶（SSS）活性和采收期的淀粉含量,从而导致了碳积累代谢的紊乱,最终造成碳积累的减少。     

遥感和GIS支持的土地利用动态监测研究——以黄河三角洲垦利县为例

以黄河三角洲垦利县为例,对比分析了目视解译、机助分类等遥感土地利用信息提取方法,采用1981、1991和1995年3时相土地利用现状信息,研究确定了统一的监测分类系统,提出了土地利用面积及其空间分布动态监测方法.在此基础上,分析了垦利县地类面积增减变化,在GIS支持下分析了1981～1995年土地利用空间动态变化,同时进行了实地监测点土地利用变化分析,探明了该县土地利用动态变化规律.     

Beta-C-glycosiduronic acids and beta-C-glycosyl compounds: new PTP1B inhibitors

Beta-C-glycosiduronic acid quinones and beta-C-glycosyl compounds have been synthesized as sugar-based PTP1B inhibitors. Benzoyl protected quinone derivatives (14 and 35) as well as aryl beta-C-glycosyl compounds (18, 22, 23 and 34) showed IC(50) values of 0.77-5.27 microM against PTP1B, with compounds 18 and 23 bearing an acidic function being the most potent.     

The chemistry of boron and its speciation in plants

The chemistry and usage of B, as well as its speciation in plants, are reviewed. In the context of biology, the chemistry of the surprisingly rare element B is dominated by B-oxygen compounds. The occurrence, distribution and chemistry of these compounds are briefly described. In addition, the chemistry involved in the interaction of B–O compounds with naturally occurring molecules, particularly polyhydroxy compounds, is summarised. The essentiality of B in plants has been known for 75 years, but the biomolecule(s) with which it interacts to cause its essential function(s) remain largely unknown, although many have been suggested. Recent research on the complexation, isolation and partial characterisation of B complexes of polysaccharides, diols, and hydroxyacids is outlined. The particular importance of B interactions with cell wall components, membranes, enzymes, sugars, and polyols is discussed.     

The design of non-peptide human bradykinin B2 receptor antagonists employing the benzodiazepine peptidomimetic scaffold

The Bradykinin B2 receptor antagonist HOE 140 (D-Arg-Arg-Pro-Hyp-Gly-Thi-Ser-D-Tic-Oic-Arg) has been used as a template for the de novo design and synthesis of a small number of non-peptide lead compounds based on the 1,4-benzodiazepin-2-one framework. Two of the compounds have been found to exhibit moderate K(i) values of 8.9 and 9.2 microM at the human Bradykinin B2 receptor.     

Phenolic compounds in Norway spruce as affected by boron nutrition at the end of the growing season

The increase in concentrations of phenolic compounds in boron (B) deficiency has been demonstrated in many herbaceous plant species, but information on woody plants is scarce. It has been suggested that accumulation of phenolic compounds plays a role in the development of cold hardiness in herbaceous plants but also that B deficiency decreases winter hardiness. Here we study the effects of B nutrition on phenolic compounds in Norway spruce (Picea abies L.) in the course of cold acclimation. Phenolic compounds were analysed in Norway spruce seedlings from three different B-fertilisation treatments in two harvests: non-acclimated and cold-acclimated seedlings. Norway spruce phenolic compounds consisted mainly of condensed tannins. During B deficiency, condensed tannins and monocoumaroyl–astragalin der. 1 increased in non-acclimated seedlings. The increase in tannins was 21%, which was nearly significant. However, the effect of B on phenolic compounds was almost absent in cold-acclimated seedlings. The condensed tannin concentration increased much more with time in the simulated autumn than due to B deficiency, and we conclude that the B effect was probably not large enough to be important for the hardening of the seedlings. The total phenolic concentrations more than doubled during the course of cold hardening suggesting that phenolics have a role in the winter hardiness in Norway spruce.     

SAR studies of some acetophenone phenylhydrazone based pyrazole derivatives as anticathepsin agents

Cathepsins have emerged as promising molecular targets in a number of diseases such as Alzeimer’s, inflammation and cancer. Elevated cathepsin’s levels and decreased cellular inhibitor concentrations have emphasized the search for novel inhibitors of cathepsins. The present work is focused on the design and synthesis of some acetophenone phenylhydrazone based pyrazole derivatives as novel non peptidyl inhibitors of cathepsins B, H and L. The synthesized compounds after characterization have been explored for their inhibitory potency against cathepsins B, H and L. The results show that some of the synthesized compounds exhibit anti-catheptic activity with K_i value of the order of 10⁻¹⁰ M. Differential inhibitory effects have been observed for cathepsins B, H and L. Cathepsin L is inhibited more pronounced than cathepsin B and cathepsin H in that order.     

Boron sources, speciation and its potential impact on health

The behaviour of boron (B) and its fate in the environment remains in many respects obscure. The major B sources and fluxes seem to have been identified, although there are many uncertainties about the magnitude and importance of each; published evaluations vary greatly. Little is known about B speciation of living matter-bearing formations, i.e. soils, natural waters, and sediments. Many authors suppose that B in nature occurs only as oxo-compounds, although, natural inorganic and organic B compounds and complexes have been described. Moreover, the most common approach to B biogeochemistry in terms of inorganic B compounds (as boric acid and borates) seems to oversimplify the matter. Data on the physiological functions of B are fragmentary and often contradictory. Some data exists on endemic symptoms and diseases among humans and grazing cattle that are supposedly triggered by B abundance in the natural environment. Unfortunately, the published data are scarce and vague. In this paper, we review the up-to date references on B sources, turnover, and speciation in the environment and the element potential impact on health.     

Determination of the absolute configurations of synthetic daunorubicin analogues using vibrational circular dichroism spectroscopy and density functional theory

The absolute configurations of three synthesized anthracycline analogues have been determined using vibrational circular dichroism (VCD) spectroscopy and the density functional theory (DFT) calculations. The experimental VCD spectra of the three compounds have been measured for the first time in the film state, prepared from their CDCl₃ solutions. Conformational searches for the monomers and some dimers of the three compounds have been performed at the DFT level using the B3LYP functional and the 6‐311G** and 6‐311++G** basis sets. The corresponding vibrational absorption and VCD spectra have been calculated. The good agreement between the experimental and the calculated spectra allows one to assign the absolute configurations of the three compounds with high confidence. In addition, the dominant conformers of the three compounds have also been identified. Chirality, 2010. © 2010 Wiley‐Liss, Inc.     

Bioactive apocarotenoids from Tectona grandis

The bioactive fractions of Tectona grandis have yielded seven apocarotenoids, two of which have been isolated for the first time as natural products (tectoionols A and B). The chemical structures were determined through 1D and 2D nuclear magnetic resonance experiments. The absolute configuration of tectoionol A was determined using a modified Mosher methodology. Some NMR assignments for the compounds 9(S)-4-oxo-7,8-dihydro-beta-ionol and 3beta-hydroxy-7,8-dihydro-beta-ionone have been corrected on the basis of g-HSQC and g-HMBC experiments. The general bioactivities of isolated compounds have been studied using etiolated wheat coleoptiles. Those compounds that presented higher levels of activity were assayed on standard target species (Lactuca sativa, Lycopersicum esculentum, Lepidium sativum and Allium cepa).     

Ohioensins F and G: protein tyrosine phosphatase 1B inhibitory benzonaphthoxanthenones from the Antarctic moss Polytrichastrum alpinum

Ohioensins F and G (1 and 2), two new benzonaphthoxanthenones, have been isolated from the MeOH extract of Antarctic moss Polytrichastrum alpinum by various chromatographic methods. The structures of these compounds were determined mainly by analysis of NMR spectroscopic data. The known compounds ohioensins A and C (3 and 4) were also obtained. Compounds 1-4 showed potent inhibitory activity against therapeutically targeted protein tyrosine phosphatase 1B (PTP1B). Kinetic analysis of PTP1B inhibition by ohioensin F (1) suggested that benzonaphthoxanthenones inhibited PTP1B activity in a non-competitive manner.     

Interaction of ganoderic acid on HIV related target: molecular docking studies

Finding the ultimate HIV cure remain a challenging tasks for decades. Various active compounds have been tested against various components of the virus in the effort to halt the virus development in infected host. The idea of finding cure from known pharmacologically active natural occurring compounds is intriguing and practical. Ganoderma lucidum (Ling-Zhi or Reishi) is one of the most productive and pharmacologically active compounds found in Asian countries. It has been used traditionally for many years throughout different cultures. More than a decade ago, el-Mekkawy and co-workers (1998) have tested several active compounds found in this plant. They have successfully identified several active compounds with reasonable inhibitory activity against HIV protease however; no further studies were done on these compounds. This study aimed to elucidate interactions for one of the active compounds of Ganoderma lucidum namely ganoderic acid with HIV-1 protease using molecular docking simulation. This study revealed four hydrogen bonds formed between model34 of ganoderic acid B and 1HVR. Hydrogen bonds in 1HVR-Model34 complex were formed through ILE50, ILE50', ASP29 and ASP30 residues. Interestingly similar interactions were also observed in the native ligand in 1HVR. Furthermore, interactions involving ILE50 and ILE50' residues have been previously identified to play central roles in HIV-1 protease-ligand interactions.These observed interactions not only suggested HIV-1 protease in general is a suitable target for ganoderic acid B, they also indicated a huge potential for HIV drug discovery based on this compound.