奶牛乳房炎多联苗(B)的临床免疫试验

用奶牛乳房炎多联苗 (B)免疫家兔 ,14 d血清中金黄色葡萄球菌抗体效价可达 1∶ 8,2 8d抗体水平明显升高 ,可达 1∶ 32 ,注苗后 35 d攻毒 ,攻毒后 2 d保护率为 93.3% (14 /15 ) ,自然保护率为 2 0 % (1/5 ) ,10 d保护率为 6 6 .6 % (10 /15 ) ,自然保护率为 2 0 % (1/5 ) ;用多联苗 (B)臀部肌肉注射免疫泌乳牛 ,试验期间 4个月内 ,3ml剂量组临床型乳房炎月平均发病率为 11.0 9% ,其对照组为 2 0 .19% ,发病率降低 4 5 .2 9% ,差异极显著 (P<0 .0 1) ;5 m l剂量组月平均发病率为 13.0 1% ,其对照组为 31.36 % ,发病率降低 5 8.5 1% ,差异极显著 (P<0 .0 1) ;3ml剂量组与 5 m l剂量组之间发病率无明显差异 (P>0 .0 5 ) ;注苗后泌乳牛血清抗体水平可持续 4个月 ,且 30 d时效价水平最高。     

番茄斑萎病毒(TSWV)广州分离物生物学特性研究

 1984年南方花生病害调查,发现由番茄斑萎病毒(TSWV)引起的新病害。     

月季抗白粉病资源的筛选

通过对月季11个品种的抗白粉病鉴定，筛选出5个免疫品种、1个高抗品种（HR）、2个中抗品种（MR）、3个高感品种（HS）。     

我国经济林应对绿色技术壁垒的战略

我国经济林发展很快，但由于产地生态破坏、环境污染以及林农的不良耕作等原因，使按常规方式生产的产品安全质量下降，从而遇到了绿色技术壁垒的严峻挑战。只有抓住机遇，认真实施无公害生产，开发安全森林食品，才能拓展产品的国际国内市场，使我国经济林产业开发再上新台阶。     

小麦远缘杂交后代节燕98-2分离类型贮藏蛋白的研究

采用A-PAGE和SDS-PAGE聚丙烯酰胺凝胶电泳方法,对远缘组合分离出来的节燕98-2类型入选11个遗传性基本稳定的具有高产、多抗的小麦株系的醇溶蛋白和高分子量谷蛋白亚基进行了分析.结果表明,在A-PAGE电泳分析中,11个供试株系具有11种不同的醇溶蛋白带型.在SDS-FAGE电泳分析中,出现了7种不同的高分子量谷蛋白亚基(HMW-GS)及6种亚基组合类型,优质亚基及亚基组合所占的比例较少,品质评分偏低,其变幅为5～8分,平均为6.36分.但在所分析的材料中,出现了一个少见的特殊亚基:2 10 12.并研究了这些HMW-GS和组合频率及特点.11个株系中7个具有45 10优质亚基和2个具有2*亚基,它们可供小麦优质育种利用.研究表明,通过远缘杂交能够选育出具有高产、抗病和优质的小麦新材料.     

干旱区20个紫花苜蓿品种抗旱性研究

该试验测定了20个苜蓿品种的水势、总含水量、自由水量、束缚水量、束/自比以及渗透调节物质.从植物水分生理与生化方面,测试各品种的抗旱性,并结合产草量、品质进行综合评价.从中选出5～6个抗旱性较强、产草量高、品质较好的苜蓿品种,为干旱区选择适宜的苜蓿品种提供具有实用价值的基础资料.     

丛生竹防霉处理研究

通过选用多种防霉剂,采用不同的处理方法来对丛生竹进行防霉处理,分别进行室内存放1 a后检验和恒温恒湿箱快速检验来判定防霉效果,对几种处理方法的优缺点进行比较,从中筛选出针对不同使用场合处理的优良防霉剂。     

狐狸脑炎病毒的分离鉴定

通过ＭＤＣＫ传细胞从黑龙江某狐场疑似狐狸脑炎病狐的肝脏中分离到对本动物具有较强致病能力的强毒株,定名为ＦＥＶ－Ｈ。经系统鉴定,并与已知国内分离毒株狐狸脑炎病毒ＦＥＶ－８８０１,狐喉气管炎病毒ＦＡＶ－２比较,证实为狐狸脑炎病毒,属犬１型腺病毒（ＣＡＶ－１）。     

糯米糍荔枝果实内源激素与落果的关系

以糯米糍荔枝生理落果期的田间调查和胚胎发育研究为基础,探讨了内源激素与生理落果的关系.结果表明,糯米糍生理落果高峰的主要原因是:第1次因授粉受精不良导致的生长促进类激素尤其是CTK水平过低;第2次与胚乳为胚的发育所利用而消失、IAA和GAs急剧降低有关;第3次与胚的败育造成CTK、GAs和IAA的全面下降有关;第4次发生在假种皮(果肉)迅速生长期,与种皮和假种皮ABA升至高水平有关.此外,还探讨了ABA /(IAA+GAs+CTK)与生理落果的相关性,以及胚囊、珠被和假种皮等果实内部组分内源激素的变化特点.     

‘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.