饲料粮比重加大中国的粮食安全性会更高

一、关于粮食问题的几个判断1、口粮消费总量将维持稳定。在相当长一个时期,中国的口粮消费总量,基本维持稳定。随着人们生活水平的提高,城乡口粮直接消费下降。1981年城乡居民人均口粮消费分别为145公斤和256公斤;2005年城市居民口粮消费只有77公斤,农民全年平均口粮消费208.9     

德国牧羊犬pose步造型及影像拍摄

德国牧羊犬是世界著名犬种，引入我国已有数十年的历史。虽然大家对德国牧羊犬已有较深入地了解研究，但对于能够凸显德国牧羊犬外貌特征、形体结构及健康状况的pose步造型及影像拍摄方面，尚未有专题介绍，而这确又是饲养、训练德国牧羊犬成就具有直接表征意义的重要体现。     

美味侧耳五种酶的同工酶谱在不同菌体组织中的变化

比较了美味侧耳不同菌体组织中５种酶的同工酶谱变化。酯酶（Ｅ５Ｔ）和苹果酸脱氢酶（ＭＤＨ）在子实体中的酶带数和活性均高于液培菌丝。过氧化物酶（ＰＯＤ）的情况则正好相反。乙醇脱氢酶（ＡＤＨ）和山梨醇脱氢酶（ＳＯＤＨ）的酶带只在子实体中发现。酶谱随子实体部位而变异的进度同酶种类有关，ＰＯＤ变化较大，ＥＳＴ和ＭＤＨ较不明显，ＡＤＨ和ＳＯＤＨ没有变化。本实验结果为今后以这５种酶为生化遗传标记研究美味侧耳提供了基础依据。     

香菇纤维素酶和半纤维素酶的热效应

本文测定了温度对香菇胞外纤维素酶和半纤维素酶活性的影响。木屑基质培养90天的香菇胞外游纸纤维素酶（C_1酶）、羧甲基纤维素酶（C_X酶）和半纤维素酶（H_C酶）的最适作用温度分别是55℃、55～60℃和50℃。在50～55℃条件下保温1小时后,C_1酶和H_C酶活性大幅度下降,而C_x酶活性下降较为缓慢,具有较高的热稳定性。本文提出相对活力系数（Relative activity coefficient,RAC）作为表示香菇菌丝生长温度与酶最适作用温度之间关系的一个参数。     

放牧系统的稳定性与载畜量的研究

本文研究了具有不同消费函数的放牧系统的稳定性,并确定出相应的系统的安全容纳量和最大容纳量。本文中有些结论改进并推广了Noy—Mcir于1976年得到的关于载畜量的有关结论。     

木质纤维素的降解和五种酶的活性对香菇子实体形成的影响

本文从生化角度研究了F型(形成子实体)和N型(不形成子实体)两类香菇菌株在生长发育过程中生化代谢活动上的差异。结果表明,在香菇的整个生长过程中,F型菌株的纤维素酶、半纤维素酶、漆酶、酸性蛋白酶和果胶酶的活性均高于N型菌株,尤其在形成子实体的第二和第三阶段,纤维素酶、半纤维素酶和酸性蛋白酶的活性均呈较大幅度的增加,这种趋势与胞外可溶性蛋白含量的增幅是一致的,同时F型菌株对培养基中木质素、纤维素和半纤维素的降解能力也高于N型菌株,说明在形成子实体的过程中,F型菌株具有比N型菌株相对更强的生化代谢能力;各种与物质降解有关酶的代谢活动在某些环节上受阻或不能有效地表达是N型菌株不能形成子实体的一个重要生理原因。     

大豆叶面积变化对田间微气象条件及产量的影响

作者通过1977～1981年和1987～1989年,分别在绥化、哈尔滨和合江地区的田间试验和生产调查,发现大豆叶面积指数的大小可造成不同的田间微气象环境条件,叶面积指数6左右时,植株似倒非倒,株间采光量和CO_2分布较为合理,光合效率高,大豆单株生育良好,群体产量高;在生产上可依据当地土地条件、施肥水平、不同品种和不同种植方式用叶面积动态变化方程式计算出适宜的密度,以使大豆群体最大叶面积指数保持在6左右,创造较理想的田间微气象效应。     

水稻不育系粒黑粉病普遍率与严重度间的关系

 稻粒黑粉病(病原菌Neovossia horrida (TaK.)Padw. et A. Kahn)是杂交稻繁殖制种田不育系上的主要病害,流行频率高,危害损失大。普遍率和严重度的关系(I-S关系)是植病流行学观测技术上的一个重要问题。     

桑树新品种育71-1的育成初报

育71—1是通过杂交、单株选择、株系选择和品比试验等一系列选育程序,培育成功的新桑树品种。其主要经济特性与湖桑32号相比,发芽期早2—3天,发芽率提高28.7％,产叶量提高47.7％,叶质较优,丝质成绩相仿;抗旱性较强。目前,正在江苏的海安、溧阳及山东等部分地区试种。     

‘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.