Cloning of plasma membrane H-ATPase gene in Populus euphratica Oliv.

For this paper, the plasma membrane (PM) H -ATPase gene has been cloned from Populus euphratica Oliv. through a homology based strategy. The isolated 3,210 bp cDNA contains a single 2,862 bp open reading frame (ORF) which encodes a putative H -ATPase protein of 953 amino acid residues, with a significant homology to plasma membrane H -ATPase of Primus persica, Phaseolus vulgaris, Sesbania rostrata and Daucus carota. The predicted protein has a molecular weight of 104,553 Da. The copy number analysis revealed multiple copies of the PM H -ATPase in the P. euphratica genome after digestion of their genomic DNA by the restriction enzymes EcoRI, NdeⅠ, FbaⅠand BglⅡ, and Southern blot.     

通过农杆菌介导法将口蹄疫结构蛋白全长基因P1导入大豆的研究

本研究以大豆体细胞胚为受体。用农杆菌介导法将口蹄疫病毒结构蛋白全长基因P1导入大豆基因组中．获得了抗性植株。经GUS染色、PCR及PCR-southern杂交等分子检测。证明目的基因已导入并整合到大豆基因组中。为利用大豆作为生物反应器生产口蹄疫新型口服疫苗奠定了基础。     

可控止回阀水力特性的测试研究

本文运用水流相似原理，对可控止回阀的流阻系数曲线和动水力矩，进行了系统的水力模型试验研究，为该阀的节能效益和技术开发的可行性，提供了必要的科学依据，其流阻系数值为０．１９，优于液控蝶阀。     

Influence of the Indoleacetic Acid-Lysine Synthetase Gene (iaaL) of Pseudomonas syringae subsp. savastanoi on Yield Attributes of Potatoes

The iaaL gene of Pseudomonas syringae subsp. savastanoi encodes an indoleacetic acid-lysine synthetase which conjugates free indoleacetic acid (IAA) with lysine. lAA-lys is biologically less active than free IAA. The iaaL coding region was expressed under the control of the cauliflower mosaic virus 35S promoter and transgenic potato plants were produced (Spena et al. 1991). 35S iaaL potato plants are characterized by increased internodal length and epinastic bending of older leaves. In three greenhouse experiments with plants grown in pots of different size and in two growth chamber experiments tuber number increased in iaaL transgenic plants compared to untransformed and vector-transformed controls of the same genotype. The increase in tuber numbers observed under controlled conditions was reflected in tuber yield which increased in the pot grown transgenics.     

樟子松松针锈病病原菌的鉴定

1989年在黑龙江省阿城市料甸林场,用樟子松(Pinus sylvestrisvar. mongolica Litv.)松针上的春孢子向健康的黄药(Phelledendron amurenseRupr.)和紫花铁线莲(Clematis fusca var. violacea Maxim)叶片人工接种成功。用人工接种所产生的夏孢子向相同寄主植物接种后,再次发病并产生夏孢子。由此证明阿城市料甸林场樟子松松针锈病菌(Cleosporium clematidis Barcl.)的转主寄主为紫花铁线莲和黄药,病原菌种应为铁线莲鞘锈菌(Coleosporium clema(?)idis Barcl.)。     

电阻电桥传感放大器性能的改善

在构成基本型电阻电桥传感放大器的基础上给出了三种改善其性能的方法。１）补偿法。２）补偿加放大器改进综合法。３）负反馈法。通过实验证明了理论分析和实际效果是一致的，从而对电阻传感器在非电量检测中的广泛应用具有一定的实际意义。     

强毒小肠结肠耶氏菌生物素标记基因探针的研究

在构建的小肠结肠耶氏菌毒性质粒DNA基因文库pYB1～8与pYP1～6的基础上,筛选出了pYB7和pYP6克隆株.用限制性内切酶Bam HI消化pYB7,Pst消化pYP6,可分离出3.8kb和6.4kb的插入性DNA片段.以这两个基因片段为目的基因,用生物素化dUTP和光敏生物素标记,获得了生物素标记的基因探针.该探针能检出10pg以上的强毒小肠结肠耶氏菌DNA,不与无毒小肠结肠耶氏菌及大肠杆菌、鼠伤寒沙门氏菌、金黄色葡萄球菌等18种对照菌反应,具有高度的特异性和敏感性.pYB7与pYP6探针对不同血清型及来源的小肠结肠耶氏菌检测,其结果与自凝性试验、依钙试验等结果相符;对小肠结肠耶氏菌强毒株与无毒株检定的准确率为100%.     

表达序列标签（ESTs）及其应用

表达序列标签(ESTs)是指从(ESTcDNA文库中随机挑取克隆并对其3’或5’端进行单轮自动测序所获得的短cDNA库列，一般长度为300～500bp。要有效获取ESTs，必须对cDNA文库进行预处理，处理方法有衰减杂交法、均一化法和差异显示法。在dbEST中收录了大量各种生物的ESTs。ESTs广泛应用于鉴定基因、发现新基因、电子克隆、构建遗传学图谱、制备DNA芯片、分子标记、研究基因的差异表达及检验病原微生物等方面。     

微生物诱导剂浸种对小麦萌发期的抗旱诱导效果

试验结果表明,在正常供水和水分胁迫条件下,经微生物诱导剂处理,可增加小麦萌发时期的根冠比,而且在水分胁迫条件下的增加幅度大于正常供水条件。微生物诱导剂可在水分胁迫条件下促进根系生长发育,提高根系干物质积累。这些性状的改善有利于提高小麦的抗旱能力。但诱导剂处理后在一定程度上抑制了小麦种子萌发率以及小麦芽和根的伸长生长。     

Genetic Engineering Approaches to Pig Production*

Modern biotechnology promises a number of new applications in animal breeding and production. Although conventional pig breeding has achieved a high level of efficiency and productivity numerous problems have been encountered with animal health and the loss of meat quality. Selection based on phenotypic performance data of individual animals does not take into account the importance of specific genes and their relevance within a complex regulatory system. In most cases it is therefore difficult to trace back the genetic origins of clinically important disorders. The application of genetic engineering techniques in pig production will facilitate diagnosis, improvement of productivity, and animal health by allowing direct genetic manipulation. Attention must be focussed on the physical and genetic analysis of the procine genome. The isolation and characterisation of genes, DNA-markers, polymorphic DNA-fragments, and their chromosomal assignment will be important prerequisites and tools for the elucidation of genetic disorders. Especially the detection of heterozygous carriers of recessive disorders and their elimination from the breeding stock will increase selection accuracy and decrease the generation intervals. But also the rapid and simple detection of infectious diseases, which is sometimes difficult if not impossible at present, will improve animal health and welfare. Although the production of transgenic animals either by DNA-microinjection into zygotes or the use of embryonal stem cells manipulated in vitro is less straightforward than DNA-based diagnosis it will play an important role in the direct manipulation of the porcine genome and genes. Breeding programmes including the use of transgenic livestock have already been developed. There is no doubt that genetic engineering has reached a degree of practical feasibility, allowing it to play an important role in pig breeding in particular and animal production in general.