真核表达载体构建表达ＰＲＶ闽Ａ株gE基因表位抗原编码区片段的重组质粒

根据伪狂犬病病毒闽Ａ株gE基因表位抗原编码区的序列与身份种真核表达载体pPICZaA、pAcGP67A序列与特性分别设计了两对ＰＣＲ引物。通过ＰＣＲ方法扩增到了两端具有不同酶切位点的gE基因表位抗原编码片段。将这２个片段分别克隆到pPICZaA与pAcGP67A载体，转化大肠杆菌ＴＯＰ１０菌档及ＸＬ１－Ｂlue菌株，获得了含伪狂犬病病毒闽Ａ株gE基因表位抗原编码区的重组质粒pICZaA-FS与pAcGP67A-FS。序测定结果显示两个重组质粒中插入片段的大小与方向均正确。     

大白菜新品种中熟6号的选育

中熟 6号是由大白菜雄性不育系 98- 2 - 1和从丰抗 70中多代自交分离而选育出的自交系F - 3-2 - 3配制而成的优良一代杂种。抗霜霉病、病毒病与软腐病 ,生长期 6 0～ 6 5d(天 ) ,叶球叠抱、圆头、卵圆形。南方栽培平均单球质量 2 .0kg ,每 6 6 7m2 产量 4 0 0 0～ 5 0 0 0kg。     

Ei及Ei Compendex Web数据库检索方法

介绍了美国《工程索引》的概况及各种版本形式，并对其中的Ei Compendex Web数据库的检索方法进行了详细介绍。     

Photosynthate Unloading from Seed Coats of Phaseolus vulgaris L. an Attempt to Define Conditions Required for Stimulation by Abscisic Acid and Benzylamino Purine

The instablity of the stimulation of photosynthate unloading from seed coats of Phaseolus vulgaris by abscisic acid (ABA ) and benzylamino purine ( BAP ) was studied in terms of experimental conditions. ABA stimulated photosynthate unloading at pH 6 and pH 8 without close dependence upon pH. ABA at a concentration range of 10-5-10-4 mol/L displayed stimulatory effect. However, BAP revealed no effect at a concentration range of 10-6-10-4 mol/L. Experiments designed with different transport time of 14C-photosynthate indicated that ABA might act at the plasma membrane of the unloading cells. Reducing endogenous ABA level by diminishing leaf area did not facilitate the manifestation of exogenous ABA function. Potassium ion stimulated photosynthate unloading from seed coats with highest promotion at 100 mmol/L K . However, no dependence of ABA stimulation of photosynthate unloading on K was found.     

云和县雪梨产业化建设进展与思考

分析了云和雪梨产业化建设的提出背景,总结了雪梨产业化建设进程中取得的经验与方法,同时在建立土地流转机制、发挥政府在雪梨产业化进程中的作用、培植龙头企业、科技创新与推广树立精品意识等方面进行了深入的思考.     

捻转血矛线虫(H.contortus)ZJ株H11蛋白基因的克隆及序列分析

参照已发表的捻转血矛线虫H11蛋白基因序列设计引物，以H．contortuss ZJ株的总RNA为模板，进行RT—PCR扩增，成功扩增出H11基因。将PCR产物与pUCm—T载体连接后，转化DH5α感受态细胞，筛选阳性克隆并测序。序列分析表明，其核苷酸序列与国外报道的H11基因的同源性为99．5％。编码氨基酸序列具有氨基肽酶的保守序列，推测可使虫体不能获得所必需的氨基酸而导致死亡。     

PCR扩增TK基因检测鸡传染性喉气管炎病毒的研究

根据已发表序列设计一对包含鸡传染性喉气管炎病毒（ILTV）TK基因全长核苷酸的1259bp引物，对2株ILTV强毒和1株ILTV疫苗毒进行PCR扩增，均能扩增出预期大小的目的片段，酶切分析证实了目的片段的特异性，而其它禽病原体的扩增均为阴性。PCR检测ILTV DNA的最小检测量为75pg。此方法检测人工接种鸡的气管棉拭样品，均能检测到ILTV，因此可用于临诊样品鸡传染性喉气管炎病的检测和诊断。     

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.