菠萝蜜种子淀粉制备香草兰微胶囊的工艺研究

以菠萝蜜种子淀粉为壁材,采用饱和水溶液法制备香草兰精油微胶囊,以包埋产率为指标,采用响应面分析法对微胶囊的包埋条件进行优化探讨。结果表明:5个单因素中,影响最显著的因素为壁芯材比例、包埋温度和包埋时间。响应面优化得到香草兰精油微胶囊的最佳工艺条件为壁芯材比例为7.5∶1;包埋时间72 min;包埋温度54℃,此条件下的包埋产率为(95.46±0.2)%,包埋率为(76.35±0.6)%,载油量为(27.73±0.3)%。试验证明,此条件结果与模型预测值相吻合,此工艺条件可为菠萝蜜种子淀粉包埋香草兰精油微胶囊工艺提供理论依据。     

优质、高产转基因抗虫棉杂交种苏杂668的选育与栽培技术

本文概述了苏杂668的选育过程，阐明了苏杂668的特征特性、产量水平、纤维品质和抗性表现，并提出其高产栽培技术措施。     

优质、低酚棉花新品种苏棉158的选育及其高产栽培技术

介绍了苏棉158的选育过程、特征特性、产量水平、纤维品质和抗病性、抗虫性及高产高效栽培技术。     

甲苯侧链催化氯化产物分布的研究

研究了催化氯化的产物分布，试验了有关条件对产物分布的影响。结果表明：氯化程度是产物分布的主要影响因素；温度的提高，有利于苄叉二氯和苄川三氯的生成；铁离子、低温及水会导致环上的氯化；水引起水解的发生。     

原发性纵隔肿瘤及囊肿71例分析(附1例罕见胸腺瘤并发症)

71例原发于纵隔的肿瘤及囊肿,其中胸腺瘤占35.2％,畸胎瘤占23.9％,神经源性肿瘤占18.2％,其他肿瘤占22.7％。三类常见肿瘤中,以胸腺瘤恶性率最高(32％),神经源性肿瘤次之(15.4％),畸胎瘤无1例恶性。术前正确诊断25例,未能分类25例,误诊21例。本文分析了误诊原因。此外,报道1例罕见的胸腺瘤并发症。     

超级稻“三定”栽培法研究Ⅲ．不同栽培方式对超级杂交稻产量形成的影响

超级杂交稻的优化(稀植、结构施肥)栽培试验于2002-2004年在长沙进行,以比较不同栽培方法对超级杂交稻产量及物质生产的影响。以两优培九为材料,并以汕优63作为对照。结果表明,两种栽培法,两个供试品种的产量表现不同,其中两优培九采用优化栽培单产为8.20～10.37t/hm2,比传统栽培增产显著。主要表现为有效穗多,而结实率、千粒重、穗实粒等产量因子差异不明显。汕优63采用优化栽培单产比传统栽培减产0.37%～8.8%。两种栽培方法间的茎蘖发生动态和单株分蘖数存在极显著差异,两组合单株分蘖数优化栽培比传统栽培分别多110.36%和110.64%,但由于移栽密度不同,两种栽培方式间的单位面积分蘖数没有明显差异。两优培九采用优化栽培的在各个生育时期,植株体内的含氮量比传统栽培的高。     

辣椒主要病害抗性的配合力分析

本文用6个亲本,按(1/2)n(n-1)双列杂交法配制15个杂交组合,对辣椒TMV、CMV、疫病、疮痂病抗性进行了配合力分析。结果表明,不同亲本、不同病害抗性的一般配合力效应和不同杂交组合的特殊配合力效应差异较大,疫病抗性显性方差所占份量较大,加性方差所占的份量较小;CMV和疮痂病抗性是加性方差所占份量较大,显性方差所占份量相对较小;TMV抗性介于二者之间。不同病害抗性间所有一般配合力的相关系数均未达到显著水平;特殊配合力是CMV与疮痂病阃的相关达到了极显著水平,TMV与CMV间和疫病与疮痂病间的相关系数达到显著水平。     

‘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.