精子肽的固相合成及应用初探

目的 :探讨将多肽固相合成技术用于检测抗精子抗体的ELISA试剂盒制备。方法 :以多肽固相合成法合成特异性精子肽 ,并经高效液相纯化分析及质谱分析。以此合成精子肽包板制备检测抗精子抗体的ELISA试剂盒 ,检测血清标本的AsAb。结果 :HPLC结果显示 ,合成的精子肽纯度达 98.26%;质谱分析结果主峰分子质量与理论值一致。采用合成多肽抗原建立了检测抗精子抗体的酶联免疫吸附测定方法 ;不明原因不育患者组与对照组间AsAb发生率呈非常显著差异(P <0,005 )。结论 :本固相合成法可获得高纯度特异性精子肽 ;该精子肽包板的ELISA试剂盒可靠简便。     

烟草青枯病危害对烟田中小型土壤动物群落的影响

为了掌握重庆植烟区烟草青枯病危害对烟田中小型土壤动物群落结构及多样性特征的影响,分别于2015年3月烟田休耕期、6月烟株旺长期和9月烟叶成熟期在重庆市彭水县进行了定点实验,调查了烟草青枯病连续成灾烟田及其对照无青枯病危害烟田中的中小型土壤动物群落。共捕获中小型土壤动物50112只,隶属于33个类群。其中,线虫、螨类和弹尾虫构成了烟田中小型土壤动物的主体,对烟田土壤动物群落特征起决定性作用。不同季节青枯病田及其对照田土壤动物整体数量表现为3月6月9月。两类烟田不同季节的土壤动物及其主要类群相对多度和密度,以及群落Margalef丰富度指数、Shannon-Wiener多样性指数、Pielou均匀度指数和Simpson优势集中性指数均表现出了明显的动态变化,且出现了显著性差异(P0.05)。群落相似性分析显示,两类烟田土壤动物群落组成相似度高,但烟草青枯病危害加剧会使相似度降低。群落稳定性结果表明,6月和9月对照田稳定性均要明显大于青枯病田。螨类与弹尾虫个体数的A/C比值均为对照田大于青枯病田,且3月和6月差异显著(P0.05)。主成分分析(PCA)表明,青枯病危害对土壤动物个体数、土壤动物密度、中气门亚目、甲螨亚目、线虫、啮虫目和棘跳虫科以及螨类与弹尾虫个体数的A/C比值影响较大;而这些对青枯病危害反应敏感的土壤动物指标,可作为青枯病发生和危害程度评价的特征指标;另外,基于PCA得分的土壤样品采集点排序结果进一步指出,两类烟田土壤动物群落组成的异质性随着青枯病危害程度的加剧而加大。上述结果说明土壤动物群落组成和多样性特征与青枯病的发生和危害密切相关;在农业生产上要开展可持续和有效的烟草青枯病生物防治,应不断加强该病原菌与土壤中小型动物生态关系的基础研究。     

卷叶薄齿藓和北美赤藓形态特征及其地理新分布

通过对采自贵州省梵净山和内蒙古赛罕乌拉自然保护区的苔藓植物标本进行鉴定,发现了丛藓科的2个新分布种——卷叶薄齿藓(Leptodontium pungens)和北美赤藓(Syntrichia amphidiacea)。卷叶薄齿藓为中国新记录种,首次在中国贵州省梵净山发现,其主要特征为茎无中轴分化,具透明层,常分布于火山和温带高海拔地区。北美赤藓为内蒙古新分布种,发现于内蒙古赛罕乌拉自然保护区,其主要特征为叶腹面近叶尖处生有大量芽胞,成熟芽胞棕色,多细胞,圆柱状。本研究对卷叶薄齿藓和北美赤藓的形态特征和地理分布进行了具体描述,并提供了图版和分种检索表。     

Effects of BmCPV Infection on Silkworm Bombyx mori Intestinal Bacteria

The gut microbiota has a crucial role in the growth, development and environmental adaptation in the host insect. The objective of our work was to investigate the microbiota of the healthy silkworm Bombyx mori gut and changes after the infection of B. mori cypovirus (BmCPV). Intestinal contents of the infected and healthy larvae of B. mori of fifth instar were collected at 24, 72 and 144 h post infection with BmCPV. The gut bacteria were analyzed by pyrosequencing of the 16S rRNA gene. 147(135) and 113(103) genera were found in the gut content of the healthy control female (male) larvae and BmCPV-infected female (male) larvae, respectively. In general, the microbial communities in the gut content of healthy larvae were dominated by Enterococcus, Delftia, Pelomonas, Ralstonia and Staphylococcus, however the abundance change of each genus was depended on the developmental stage and gender. Microbial diversity reached minimum at 144 h of fifth instar larvae. The abundance of Enterococcus in the females was substantially lower and the abundance of Delftia, Aurantimonas and Staphylococcus was substantially higher compared to the males. Bacterial diversity in the intestinal contents decreased after post infection with BmCPV, whereas the abundance of both Enterococcus and Staphylococcus which belongs to Gram-positive were increased. Therefore, our findings suggested that observed changes in relative abundance was related to the immune response of silkworm to BmCPV infection. Relevance analysis of plenty of the predominant genera showed the abundance of the Enterococcus genus was in negative correlation with the abundance of the most predominant genera. These results provided insight into the relationship between the gut microbiota and development of the BmCPV-infected silkworm.     

中国瑞脊菱蜡蝉属一新种（半翅目：菱蜡蝉科：五胸菱蜡蝉族）

记述中国已知瑞脊菱蜡蝉属Reptalus 3个种,其中包括1新种:顺溪坞瑞脊菱蜡蝉Reptalus shunxiwuensis sp.nov.。编制了分种检索表。模式标本保存于西北农林科技大学昆虫博物馆。     

沼泽红假单胞菌生物合成银纳米粒子及其抗菌作用

近年来,利用沼泽红假单胞菌合成银纳米粒子作为一种可靠和环境友好的方法出现。主要利用沼泽红假单胞菌的细胞滤液来还原银离子。制备的纳米粒子用紫外可见光谱(UV-vis)、X射线衍射光谱(XRD)和透射电镜(TEM)进行表征。含有银粒子溶液的UV-vis光谱显示在420 nm-460 nm处出现银纳米粒子的吸收峰。TEM图像表明所形成的银纳米粒子的粒径范围为5 nm-20 nm。纳米粒子的XRD图谱证明产物为金属银。所制备的银纳米粒子对大肠杆菌和金黄色葡萄球菌作抑菌性试验。     

何首乌中新的二苯乙烯甙

用反相层析法从何首乌（Polygonum multiflorum Thunb.)根茎的水提物只发得2个新的二苯乙烯甙（1,2）及9个已知化合物：没食子酸（3）,2,6－二羟基－苯甲酸（4）,吲哚－3－（L－）α氨基－α－羟基－丙酸）甲酯（5）1,2－二羟基丙烷－1－（4－羟基－苯基）（6）,大黄素（7）,大黄素－8－β－D－葡萄糖甙（8）,（＋）－lyoniresinol-3α－O－β－D－葡萄糖甙（9）,2,3,4、,5－四羟基反式二苯乙烯－2－O－β－D－吡喃葡萄糖甙（10）和2,3,4',5－四羟基反式二苯乙烯－2,3,－二－O－β－D－吡喃葡萄糖甙（11）。亲化合物结构通过理化性质与波谱分析特别是2D NMR得以确定。化合物2表现出很强的DNA裂解活性,化合物1,2与10具有很强的抗脂质过氧化活性。     

放牧对黄河低阶地盐化草场土壤水盐空间异质性的影响

选定黄河低阶地地形大致相近的放牧草场与封育草场,按实地情况分别设置长770m（放牧）、370m（放牧）和240m（封育）3条样线,采用校正后的便携式WET Sensor以10m为间隔进行土壤水盐的分层（0～10cm,10～20cm）测定,并对其进行地统计学分析.结果表明：黄河低阶地盐化草场表层土壤水盐的变异系数和相关性高于下层,土壤水分的变异系数低于土壤盐分且层间的相关性较高;放牧使土壤水盐之间的相关程度增大,变异降低,且使土壤水分存在一定的冗余.所研究草场的土壤水盐表现为中等或强烈空间自相关,封育盐化草场水盐空间相关尺度的差异较小,而放牧草场则相反.持续放牧已经成为一种稳定影响盐化草场水盐空间分布的结构性因素,使盐化草场的水盐空间异质性减弱.盐生植物在草场内随机分布且不受放牧干扰,是封育盐化草场随机作用较强的最可能原因;而放牧草场内牲畜的啃食和践踏对盐生植物和土壤结构改变所形成的反馈作用大大降低了这些植物对水分特别是盐分的再分配,进而导致放牧草场水盐的含量趋于增大且分布格局趋于简单.     

Rapid and reliable detection of 11 food-borne pathogens using thin-film biosensor chips

Traditional methods for identifying food-borne pathogens are time-consuming and laborious, so it is necessary to develop innovative methods for the rapid identification of food-borne pathogens. Here, we report the development of silicon-based optical thin-film biosensor chips for sensitive detection of 11 food-borne pathogens. Briefly, aldehyde-labeled probes were arrayed and covalently attached to a hydrazine-derivatized chip surface, and then, biotinylated polymerase chain reaction (PCR) amplicons were hybridized with the probes. After washing and brief incubation with an antibiotin immunoglobulin G–horseradish peroxidase conjugate and a precipitable horseradish peroxidase substrate, biotinylated chains bound to the probes were visualized as a color change on the chip surface (gold to blue/purple). Highly sensitive and accurate examination of PCR fragment targets can be completed within 30 min. This assay is extremely robust, sensitive, specific, and economical and can be adapted to different throughputs. Thus, a rapid, sensitive, and reliable technique for detecting 11 food-borne pathogens was successfully developed.     

Physiological characteristics of the primitive CO2 concentrating mechanism in PEPC transgenic rice

C4 plants such as maize have CO2 concentrating mechanism and higher photosynthetic efficiency than C3 plants, especially under high light intensity, high temperature and drought conditions. In recent years, due to the rapid development of transgenic technique, different transgenic rice plants with high-level expression of C4 genes have been created by the successful introduction of genes encoding the key C4 photosynthetic path enzymes PEPC, PPDK and NADP-ME through agrobacteria-mediated…