分散松香施胶剂性能影响因素的探讨

对逆转法制备分散松香施胶剂过程中的主要因素如乳化剂的种类及用量、马来松香加合物含量、搅拌转速、加料速度和乳化温度等系统地进行了探讨，提出了合理的工艺条件，并对实际生产中可能出现的问题及解决办法进行了阐述。     

犬瘟热病毒的静水压灭活

以250MPa的静水压力对犬瘟热病毒（CDV）处理30min之后，CDV被灭活，由其制成的灭活疫苗诱导犬产生中和抗体的能力明显优于传统的福尔马林灭活疫苗，免疫保护率达90％。电镜观察显示，经不同程度静水压力处理后的CDV粒子均发生变形，表面呈现凸起，但CDV H基因部分片段的RT－PCR扩增结果揭示，高达510MPa的静水压力作用30min也未能使其基因片段受到破坏。     

国外松芽流脂病发生与防治

近年来,浙江省局部地区国外松纯林受芽流脂病危害较为严重.通过定点现察、分离培养、光镜检查、电镜现察、微量元素测定和用硼砂防治罹病松树等方法,基本查清国外松芽流脂病在浙江省的发生情况,明确了国外松芽流脂病的3种症状顶芽枯死型、丛枝型和枯梢型.国外松芽流脂病是由于松树自身和土壤中的微量元素--有效硼含量不足引起的生理性病害.用喷洒3.0g@kg-1或5.0g@kg-1硼砂溶液防治该病效果显著,防治区病情指数与对照相比平均下降38.5,松树的年平均高生长量也比对照大14.8cm.表4参4     

辛夷油的药理学研究

向大白鼠胸腔注入角叉菜胶诱发胸膜炎,8h后处死动物，测定其胸腔渗出液中白细胞数、蛋白质及前列腺素E2（PGE2）的含量，体内白细胞介素1（IL-1）和肿瘤坏死因子（TNF）的含量。结果显示，事先灌服辛夷油的试验组动物，其胸腔渗出液中白细胞数、蛋白质和PGE2的含量均显著小于模型对照组；IL-1和TNF的含量也明显小于模型组，说明辛夷油能抑制炎症介质的产生，具有抗炎效应。     

寡果糖对断奶仔猪生长、代谢和免疫的影响

在基础日粮中添加寡果糖 ,研究其对断奶仔猪生长、代谢和免疫的影响。试验将 32头杜大二断奶仔猪分为 2组 ,基础日粮为对照组 ,基础日粮添加 0 1 7%寡果糖为试验组 ,预试期 4d ,正式试验期 2 8d。结果表明 :试验组较对照组仔猪日增重提高 3 88% (P >0 0 5) ,料重比下降4 67% ;仔猪血液尿素氮含量显著升高 (P<0 0 1 ) ,甲状腺素 (T4)和白细胞介素 2 (IL 2 )含量也显著升高 (P<0 0 5) ,血糖和T3含量有升高趋势 ,但不显著     

牵引犁受力分析的解析方法

分析了牵引犁受力图解法求解所存在的问题，用解析方法建立了牵引犁受力的矩阵方程组并利用计算机进行了求解，预测了各结构参数变化对机组受力工况的影响，从而为牵引犁机组的合理配置和各部件结构的强度计算和优化设计提供了理论依据。     

火炬松短周期工业材不同高度上干缩性能的研究

对湖南同一立地指数（１８）下，５株１７．５年生的火炬松（ＰｉｎａｓｔａｅｄａＬ．）短周期工业材１．３，３．６，５．６，７．６，９．６ｍ５个高度的木材干缩系数、基本密度、生长轮宽度、晚材率和微纤丝角度，按生长轮取样，进行了测量和统计分析．结果表明，弦向、径向、体积干缩系数和干缩比，在树于５个高度之间的差异，均达到了显著水平；各高度干缩系数与生长轮的年龄（离髓心的距离）以及与上述各主要构造因子之间呈显著的线性相关，且相关度度随树干高度的增加而减弱．     

猪传染性胃肠炎病毒南京株纤突S蛋白基因的克隆与序列分析

参考 Genbank收录的 TGEV- Miller株的基因序列 ,自行设计合成 1对引物 (TGEVP5 /P6 ) ,对不同代次的 TGEV疫苗弱毒 STC3及种毒 、种毒 进行了 RT- PCR扩增 ,产物经琼脂糖凝胶电泳分析 ,均出现 1条大约 12 6 2 bp的目的条带 ,经 Eco R 酶切 ,都产生了 871bp和391bp左右的两个片段 ,与预期大小相符。将种毒 RT- PCR扩增目的条带回收纯化后克隆入PMD18- T载体中 ,转化宿主菌 DH5 α,挑选阳性克隆 (命名为 PTs) ,提取重组质粒 ,用 Hpa 、Eco R 对重组质粒进行酶切鉴定以及 PCR扩增 ,然后进行序列测定 ,并进行了序列分析 ,证实与国外标准毒株 Miller、Fs772 / 70、Purdue、TO14等有较高的同源性     

‘Plantibodies’: a flexible approach to design resistance against pathogens

Engineering resistance against various diseases and pests is hampered by the lack of suitable genes. To overcome this problem we started a research program aimed at obtaining resistance by transfecting plants with genes encoding monoclonal antibodies against pathogen specific proteins. The idea is that monoclonal antibodies will inhibit the biological activity of molecules that are essential for the pathogenesis. Potato cyst nematodes are chosen as a model and it is thought that monoclonal antibodies are able to block the function of the saliva proteins of this parasite. These proteins are, among others, responsible for the induction of multinucleate transfer cells upon which the nematode feeds. It is well documented that the ability of antibodies to bind molecules is sufficient to inactivate the function of an antigen and in view of the potential of animals to synthesize antibodies to almost any molecular structure, this strategy should be feasible for a wide range of diseases and pests.Antibodies have several desirable features with regard to protein engineering. The antibody (IgG) is a Y-shaped molecule, in which the domains forming the tips of the arms bind to antigen and those forming the stem are responsible for triggering effector functions (Fc fragments) that eliminate the antigen from the animal. Domains carrying the antigen-binding loops (Fv and Fab fragments) can be used separately from the Fc fragments without loss of affinity. The antigen-binding domains can also be endowed with new properties by fusing them to toxins or enzymes. Antibody engineering is also facilitated by the Polymerase Chain Reaction (PCR). A systematic comparison of the nucleotide sequence of more than 100 antibodies revealed that not only the 3′-ends, but also the 5′-ends of the antibody genes are relatively conserved. We were able to design a small set of primers with restriction sites for forced cloning, which allowed the amplification of genes encoding antibodies specific for the saliva proteins ofGlobodera rostochiensis. Complete heavy and light chain genes as well as single chain Fv fragments (scFv), in which the variable parts of the light (V_L) and heavy chain (V_H) are linked by a peptide, will be transferred to potato plants. A major challenge will be to establish a correct expression of the antibody genes with regard to three dimensional folding, assembly and intracellular location.     

Relationship between the intracellular calcium concentration changes and left ventricular hypertrophy and function in the spontaneously hypertensive rats

AIM:To elucidate the relationship between the intracellular calcium concentration changes and left ventricular hypertrophy and function in the spontaneously hypertensive rats (SHR).METHODS:Intracellular free calcium concentrations were measured by Fura 2 methodology and left ventricular function quantitated by cardiac catheterization in 20 SHR aged 10, 22, and 34 weeks and 20 age-matched Wistar-kyoto (WKY) rats.RESULTS:(1) The systolic blood pressure(SBP), intracellular calcium concentrations and left ventricular mass / body weight index (LVM/BW) were significantly higher in all three age groups of SHR than the corresponding groups of WKY; (2) Compared with age-matched WKY groups, the peak left ventricular pressure descending rate(-dp／dt_max) decreased while left ventricular relaxation time constant (τ)increased significantly in SHR aged 22 and 34 weeks. The peak left ventricular pressure ascending rate(dp／dt_max) and the left ventricular contractility index were significantly increased only in the 34 weeks SHR; (3) Intracellular calcium concentrations showed a positive correlation with LVM/BW,SBP,-dp／dt_max and τ(r=0.47-0.83,P<0.01)and a negative correlation with dp／dt_max and the left ventricular contractility index (r=-0.46,P<0.05 and r=-0.81, P<0.01).CONCLUSION:Intracellular calcium overload is one of the potential mechanisms in the induction of left ventricular hypertrophy as well as of systolic and diastolic dysfunction.