苹果抗病虫育种研究概况

抗病虫育种已成为许多苹果生产国苹果育种的主要目标.选育抗病虫苹果新品种可以降低生产成本,同时也可以满足生产绿色果品的需要.20世纪80年代以来,随着世界环保呼声渐高,苹果抗病虫育种研究日益受到重视,并取得了一定进展.但在我国苹果抗病虫育种研究甚少,仅在方法上进行一些探索,本文概述苹果抗病虫育种研究.     

论个性化的大学英语课程设置

讨论了目前大学英语课程设置单一的现状，并分析其形成原因。文章以ESP研究关于需求分析的理论为依据，提出大学应根据学生的实际需要、新时期国家和社会对人才培养需要，区别不同层次、不同程度、不同专业学生的需求，而专门设置一系列大学英语课程。说明了设置个性化的大学英语课程的理由和好处。     

吉林省荒地资源生态适宜性评价

本文从吉林省荒地资源的实际出发 ,在荒地资源生态适宜性评价基本理论的指导下 ,采用地理信息系统方法 ,对吉林省荒地资源进行了生态适宜性评价。通过空间数据和属性数据的融合、分析、处理 ,可以直观获得荒地资源的生态适宜度等级 ,从而提高评价效率 ,为荒地资源的合理开发利用提供科学依据。     

植物源农用杀菌剂银泰对作物刺激生长作用

本文通过应用植物源农用杀菌剂银泰的不同浓度处理草莓和菠菜，测定绿色面积指数、叶面积指数、根冠比、叶绿素含量、硝酸还原本科活性、生物产量、经济产量。结果表明，银泰对草莓和菠菜均具有明显的刺激生长作用。     

Biological characteristics of long passaging rat mesenchymal stem cells

AIM:To investigate multi-potential of rat bone marrow mesenchymal stem cells (rBMMSC) and mutation inclination, the rBMMSC were long passaged in vitro. METHODS:Cellular cycles of different passages were assayed by FACSan flow cytometry and karyotypes of passage 6, passage 25 and passage 45 were compared by G-binding analysis. RESULTS:The early passages and long-term passages all showed strong proliferation; passage 6, passage 25 and passage 45 all showed normal karyotype. CONCLUSION:Long-term culture and passage of rBMMSC still remains strong proliferation. With this capability, the mutation inclination is not enhanced.     

晋南冬麦区大麦黄矮病毒流行株系监测及防治策略探讨

连续5年(1996～2000年)采集晋南冬麦区小麦黄矮病标样,采用生物学和血清学(酶联免疫吸附法)相结合的诊断方法对该地区的大麦黄矮病毒流行株系进行了鉴别。结果表明,该小麦黄矮病流行区近五年以GAV株系为主流株系,兼有少量GPV、PAV和混合株系存在。同时对小麦抗黄矮病新品种“临抗1号”进行了GPV和GAV两种株系的抗性测定,明确了该品种兼抗GPV和GAV两种株系。根据小麦黄矮病发生现状,提出了一套以选育推广抗耐病品种为主,以药剂防治为辅的综合防治措施。以期为当地小麦生产服务。     

苹果梨中多酚氧化酶酶学特性的研究

 以苹果梨中的多酚氧化酶为研究对象, 对其酶的活性变化及其特性的研究表明, 苹果梨中的多酚氧化酶的最适pH 值是4. 6 , 最适温度是40 ℃; 亚硫酸氢钠、维生素C、柠檬酸对苹果梨中多酚氧化酶的抑制作用依次减弱, 硫酸钠几乎无抑制作用。不同底物和同底物不同浓度影响多酚氧化酶特性。     

早熟、优质、耐贮梨新品种新梨7号选育研究

以库尔勒香梨为母本,早酥梨为父本,有性杂交选育成新梨７号品种。该品种同时兼备优质、早熟与耐贮藏性;该品种遗传了父本的早熟性,比父本更早熟１５~２０ｄ,盛花期~果实可食期约８０~９５ｄ,属于早熟品种;且遗传了母本品质性状的质地酥脆、耐贮、清香、阳面红晕,比母本果个大,果心小。果柄木质化,丰产抗风。新梨７号果实贮藏期的可溶性固形物、果实重量、果实硬度和果实前期腐烂率的变化与库尔勒香梨基本相似,但耐热能力高于母本。凡适宜香梨、早酥、苹果梨和巴梨种植的地区,都适宜该品种的种植。     

Preparation of gfp-bcl-XL-contained recombinant adenovirus vector by the homologous recombination in bacteria

AIM: To prepare gfp-bcl-X_L-contained recombinant adenovirus(rAd-gfp-bcl-X_L).METHODS: Bcl-X_L gene was amplified from pEGFP-C₃-bcl-X_L, subcloned into shuttle plasmid and formed transfer plasmid of pAdTrack-CMV-bcl-X_L. Then pAdTrack-CMV-bcl-X_L was linealinzed with PmeI and co-transformed into BJ5183 bacteria with adenovirus genomic plasmid of pAdEasy-1. The identified recombinant adenovirus plasmid was digested with PacI and transfected into 293 cells to package recombinant adenovirus particles. The target gene was detected by PCR.RESULTS: There were about 35% positive recombinant bacterial clones after the co-transformation of pAdTrack-CMV-bcl-X_L and pAdEasy-1 into BJ5183. Recombinant adenovirus particle were produced and further amplified after the transfection of pAdEasy-1-gfp-bcl-X_L into 293 cells. PCR test indicated that the recombinant Ad contained bcl-X_L gene. The titer of the purified rAd-gfp-bcl-X_L was 6.5×10¹² PFU/L. CONCLUSIONS: The homologous recombination in bacteria is a convenient and high efficient method to prepare rAd-gfp-bcl-X_L. This affords a good gene transfer vector for the gene therapy in human’s diseases.     

Effects of PD98059 on the differentiation from mesenchymal stem cells to osteoblasts

AIM: To investigate the effects of PD98059 on the differentiation from mesenchymal stem cells to osteoblasts.METHODS: hMSC were separated from human marrow and expanded in cuture medium. hMSC were induced with dexamethasone, β-glycerophosphate, vitamin C which acted as osteoblast differentiation inducer. PD98059 was added into the osteoblasts induction medium. The cells were assayed with cell morphology, alkaline phosphatase (AP) activity and calcium deposition. RESULTS: The isolated cultured MSC comprised a single phenotypic population and displayed a fibroblast-like morphology. After induced with osteoblasts induction medium, the cells showed changes in cell morphology from spindle-shape to cuboidal and polygonal. The AP activity increased gradually and reached the peak in 12 days, then decreased. Many scattered tangerice calcium nodes were observed. PD 98059 significantly inhibited AP activity and calcium deposition in a dose-dependent manner. A striking observation of the present study was that a few adipocytes appeared in cultures that were treated with PD 98059 and osteogenic differentiation medium. CONCLUSION: These results indicated that osteogenic diferentiation from the hMSCs was related to the activation of the ERK.