苦豆子提取物与埃玛菌素混用对小菜蛾生长发育和繁殖的影响

将苦豆子甲醇和水提取物分别与埃玛菌素混合,在室内测定了两混合物对小菜蛾生长发育和繁殖的影响.结果表明:苦豆子甲醇提取物 埃玛菌素和苦豆子水提取物 埃玛菌素对小菜蛾3龄幼虫口服毒力明显高于埃玛菌素,其LC50值分别为0.19、0.32和0.51 mg.L-1;用两混合物以及埃玛菌素亚致死剂量处理3龄幼虫,试虫化蛹率、羽化率和成虫的繁殖力均呈现明显不良影响.     

基于土地利用/覆被变化的荒漠绿洲碳储量动态评估

以典型的荒漠绿洲区为研究对象,基于不同时期土地利用/覆被类型图,运用Bookkeeping模型,结合土壤、植被碳密度基础资料及调查数据,评估了近30年临泽绿洲土地利用/覆被变化特征及其对碳储量的影响。结果表明:(1)临泽荒漠绿洲区的土地利用/覆被变化特征主要表现为:居民及建设用地、耕地、林地呈增加趋势,增幅分别为90.2%、75%、46.5%;盐碱地、水体、沙地、荒漠草地则呈减少趋势,减幅分别为73.9%、67.8%、46.2%、5.5%。(2) 30 a耕地面积增加了269.38 km~2,其中耕地开垦面积为372.57 km~2,开垦主要来源于盐碱地、荒漠草地和沙地,分别占耕地开垦面积的24.7%、24.4%和21.05%。耕地转变为其他土地覆被类型的面积为103.19 km~2,转变后的主要去向分别是居民及建设用地、盐碱地和荒漠草地,分别占耕地转变为其他土地覆被类型面积的32.78%、17.8%和15.37%。(3)土地利用/覆被变化导致总碳储量增加5.89×10~5t,其中土壤碳储量增加量为4.02×10~5t,植被碳储量增加量为1.86×10~5t;耕地变化使碳储量增加4.91×10~5t,其中使碳储量增加的转变分别是荒漠草地-耕地、沙地-耕地、盐碱地-耕地、耕地-林地,相反的转变则使碳储量减少。总体来看,临泽荒漠绿洲土地利用/覆被面积和结构均发生了变化,耕地开垦为最主要的土地利用/覆被变化,土地利用/覆被变化导致碳储量总体呈增加趋势,耕地变化是影响碳储量变化的主要因素。     

DHPLC检测胃癌微卫星不稳定性

为探讨一种快速、简便、可靠的胃癌微卫星不稳定性（MSI）检测方法,变性聚丙烯酰胺凝胶电泳-银染法检测28例胃癌12个微卫星位点(D1S548、D1S552、D5S346、TP53、IGFIIR(G)8、IGFIIR(CT)5、TGFßRII(GT)3、TGFßRII(A)10、hMSH3(A)8、hMSH6(G)8、BAX(G)8和Bat26）,DHPLC柱温50℃检测Bat26位点。凝胶电泳发现MSI-H 2例（7.14%）,MSI-L胃癌15例（53.6%）,Bat26+2例均为MSI-H,Bat26改变和MSI-H表型一致（P<0.01,Fisher’s确切概率法）。DHPLC亦证实2例Bat26+胃癌,结果和凝胶电泳完全一致。结果表明,DHPLC检测Bat26位点是研究胃癌MSI-H的较好方法,有一定的临床应用价值。Abstact: To establish a fast, simple and solid method of studying microsatellite instability (MSI) in gastric cancer, a panel of 12 microsatellite sites,D1S548, D1S552, D5S346, TP53, IGFIIR(G)8, IGFIIR(CT)5, TGFßRII(GT)3, TGFßRII(A)10, hMSH3(A)8, hMSH6(G)8, BAX(G)8 and Bat26, were detected by denatured polyacrymide gel electrophoresis-silver stain in 28 gastric cancers. Bat26 was also analyzed by denatured high performance liquid chromatograph (DHPLC) at 50℃ in the DNASep Cartridge. Two MSI-H (7.14%) and 15 MSI-L cancers (53.6%) were identified in 28 gastric cancers. Bat26 was positive only in 2 MSI-H cancers. The alterations of Bat26 and MSI-H status were coincident (P<0.01). The two Bat26+ cancers were also confirmed by DHPLC. Results obtained from DHPLC and gel electrophoresis were completely consistent. Thus, DHPLC analysis of Bat26 site may be a favorable method of detecting MSI-H status in gastric cancer, and be of clinical importance.     

力学环境对软骨基质代谢的影响

正常关节软骨所受压力是由动态压力与静态压力交替完成。压力引起软骨一系列生理变化包括细胞及细胞外基质成分变形、组织内液体流动、水流电位和生理生化变化。这些变化直接调控细胞外基质代谢。体外构建有良好功能的组织工程化软骨是目前软骨病变、缺损理想的修复方法。研究力学环境对软骨基质代谢的影响,对构建组织工程化软骨有深远意义。     

马勃的食药用价值及其研究进展

在生物的多样性中,马勃(Puff-balls)是一类独特的大型真菌生物,是我国民间常见的用于止血、消肿的药用真菌之一。论文对马勃的真菌分类学地位及其在世界范围、我国的分布情况作了简要阐述,重点介绍了马勃的化学成分、食用价值、本草考证、药用价值及其在临床应用方面的研究进展,指出了我国马勃资源的应用前景和现存的问题。     

基于RS的湖岸带物理结构完整性评价方法——以查干湖为例

以查干湖流域为研究区,利用RS和GIS技术,基于水利部《河流(湖)健康评估指标、标准与方法 V1.0》并加以改进,以500m×1000m为评价基本单元,整个研究区共有315个物理结构基本评价单元,建立基于RS的湖岸带物理结构完整性评价体系,该评价体系由目标层、准则层和指标层构成,其中准则层由湖岸带状况、湖岸线发育率和湖泊萎缩率3项组成,指标层由地形坡度、植被覆盖率等8项指标构成。研究结果表明:38个监测点中,查干湖23个,新庙泡15个,基于RS物理结构评价结果分别为0.67—0.76和0.35—0.45,地面实测评价结果分别是0.64—0.77和0.35—0.55。两种评价方法结果一致,并表明查干湖的湖岸带物理结构健康状态属于健康,新庙泡则属于亚健康。     

普氏蹄蝠下丘谐波内外神经元处理多普勒频移补偿信息的差异

为了探讨普氏蹄蝠下丘神经元在处理多普勒频移补偿后回声定位信号中的作用,实验采用双声刺激模式模拟蝙蝠不同飞行状态下产生多普勒频移补偿后的脉冲-回声对,即发声频率改变,回声频率维持恒定的情况下,研究下丘神经元对不同补偿值下的回声反应恢复率.结果发现:根据神经元在某一补偿值下对回声信号反应的恢复率是否超过70%,可将其分为具有选择性(S)和无选择性(NS)的两类神经元.且谐波内S神经元所占比例(68%)远超过非谐波内S神经元(39%).分析神经元的发放模式发现谐波内S神经元中相位型发放模式比例(44.3%)明显高于其他三种类型神经元.另外,虽然S和NS神经元的强度-潜伏期函数类型均以饱和型为主,但谐波内S神经元强度-潜伏期函数的最佳强度(best amplitude,BA)(95.3±14.0)dB SPL低于NS神经元的BA(104.1±10.2)d B SPL(P0.01),同时也低于非谐波内S神经元的BA(109.7±7.9)dB SPL(P0.01).以上实验结果表明,在下丘水平,神经元就已对多普勒频移补偿后回声定位信号的处理有了分工,集中在谐波内的S神经元通过提高对某一补偿值下回声信号反应的恢复率实现,对回声信息的精确编码,避免其他杂波干扰信息.同时,谐波内S神经元的发放模式和强度-潜伏期函数特点也满足其在复杂环境中精确声学成像的需求.     

基于动力学模型的法夫酵母发酵生产虾青素的补料策略优化

对法夫酵母的不同补料发酵方式进行了研究.基于底物抑制模型,提出了一种优化的两阶段补料策略,用于法夫酵母产虾青素的高密度发酵.在发酵的延迟期和对数生长期早期,糖浓度控制在25 g/L左右,在此条件下,生物量可以达到最大,且时间缩短.在对数生长期后期及稳定期,糖浓度控制在5 g/L,虾青素的合成时间可以有效延长.与传统的补料方式相比,采用此补料策略取得了较好的发酵效果.发酵终点细胞干重达到23.8g/L,虾青素产量达到29.05 mg/L,分别比分批发酵提高了52.8%和109%.     

Specific endotoxic lipopolysaccharide-binding receptors on murine splenocytes. III. Binding specificity and characterization.

In previously published studies, we employed a photoreactive radioiodinated derivative of LPS from Escherichia coli 0111:B4 to identify and characterize a membrane-localized specific LPS binding protein of approximately 80-kDa molecular mass. Our more recent studies demonstrating that mAb with specificity for this 80-kDa protein will act as an agonist in mediating macrophage activation have established that this protein serves as a specific receptor for LPS. In the experiments reported here, we have more accurately determined the apparent molecular mass of this protein to be 73 kDa (p73). We have also extended the sources of LPS-derivatized photo-cross-linking preparations (including Re-LPS) to determine generality of LPS binding to this receptor. Binding to the p73 LPS receptor is demonstrated with all of the LPS derivatives synthesized in our laboratory, as well as probes synthesized by other investigators. Binding of S-LPS is readily inhibited by Re chemotype LPS, and we have shown that this competitive inhibition is most likely not the result of formation of LPS aggregates. These results confirm and extend our earlier studies suggesting that the binding of LPS to the p73 receptor is lipid A specific. We further demonstrate that, in contrast to results published in a recent report, the p73 LPS receptor has no significant binding specificity for a variety peptidoglycan polymer preparations. Finally, we show that this LPS receptor can be detected on murine fibroblast, macrophage, and mastocytoma cell lines. Differences have been observed in the level of expression of LPS receptors on the various cell lines studied.