应用花药培养技术培育苹果新类型

通过对苹果不同品种花培植株的试管苗及其高接树的染色体数目观察,看到大部分为单倍体,还有其他倍性的植株.幼龄期元帅花培植株的植物学性状与原品种元帅之间有显著差异,表现分枝多、有针刺、叶片小而薄、茸毛少、有缺刻等野生性状.在花培植株之间,也表现有明显的差别.田间高接后,花培植株随树龄增长逐渐向栽培性状转化,元帅花培植株元80—3已开始结果,表现出明显的短枝型特征.     

蛋白质组学研究技术及其在果树学中的应用

蛋白质组研究是当今生命科学发展的一个新的增长点,它能阐明基因组所表达的真正执行生命活动的全 部蛋白质的表达规律和生物功能。简要介绍了蛋白质组学产生的科学背景、研究方法和研究内容。蛋白质组学研究 方法主要有双向聚丙烯酰胺凝胶电泳(2D-PAGE)、质谱(Mass-spectrometric)技术、蛋白质芯片(Protein chips)技术、酵母 双杂交系统(Yeast two-hybrid system)、双向高效柱层析和生物信息学等。其应用的范围包括植物群体遗传学、在个体 水平上植物对生物和非生物环境的适应机制、植物的发育和组织器官的分化过程,以及不同亚细胞结构在生理生态 过程中的作用等诸多方面。同时展望了植物蛋白质组学研究前景以及蛋白质组学技术在果树学中的应用前景。     

猪生殖与呼吸综合征病毒M基因和N基因的表达

将猪生殖与呼吸综合征病毒（PRRSV）的M基因和N基因从重组质粒pMD18-T—M—N中亚克隆至pBV220原核表达栽体上，成功构建了重组表达质粒pBVM—N。将pBVM—N转化大肠埃希氏菌DH5α感受态细胞．重组菌经温度敏感诱导表达，其细菌裂解物经SDS—PAGE可检测到分子质量约为19ku的目的蛋白，与M基因表达产物一致；经蛋白质分析软件Bandscan分析，其表达量可达19．1％；Western-blotting分析表明，该重组蛋白可被兔抗PRRSV血清所识别，与预期的M基因表达产物相一致，而N基因未获表达。     

花生在饲草生产中的间作套种技术与效果研究

本文研究了紫花苜蓿、白三叶、多年生黑麦草、鸡脚草和苇状羊茅等五种多年生牧 草与花生在“5+6”模式套作情况下生长特点以及对饲草生产的影响。花生与禾草的套作能够 极显著地促进禾草的分蘖(11．01％-14．26％)(P<0．01),显著增加其叶面积指数(4．62％- 6．37％),(P<0．05)三种禾草的产草量分别提高了8．2％、8．1％、9．3％。花生秧与禾草混合 调制后,饲草中的粗蛋白、粗脂肪和钙的含量得到了显著和极显著的提高,而粗纤维含量却明 显降低。紫花苜蓿和花生套作能够提高牧草产草量5．8％,豆科牧草与花生秧混合调制以后, 粗蛋白、粗纤维以及钙和磷的含量明显下降,粗脂肪得到了极显著的提高。     

论西部大开发中张掖市生态环境建设问题

张掖市长期受干旱、大风及沙尘暴影响,生态环境极为恶劣,制约着西部大开发建设进程。其存在的重要问题是:水资源匮乏,植被破坏严重,覆盖率低等;针对具体情况提出:改善水资源条件和恢复植被是张掖地区生态环境建设的重点。     

Analysis of gene expression profile of multidrug resistant MCF/DOX cell line after benflumetol derivative LY980503 treatment

AIM:To investigate the effect of LY980503(a benflumetol derivative)on multidrug resistance of tumor cell line using DNA microarray.METHODS:Total RNA was extracted from multidrug resistant MCF/DOX cell line. cDNA microarray containing 320 cDNAs was used to detect the gene expression profile.RESULTS:9 down-regulated genes and 1 up-regulated gene were identified after multidrug resistant MCF/DOX cells were treated with LY980503.CONCLUSION:LY980503 can effectively reverse the resistance of MCF/DOX to DOX in vitro by adjusting the expression of multi-genes.     

不同地下水位植物蒸腾耗水特性研究

在甘肃省民勤治沙站利用非称量测渗仪研究了梭梭、柠条等 10种沙区植物的蒸腾耗水特征。结果表明 ,各种植物 5a的总蒸腾量由大到小排列为 :沙枣、花棒、沙木蓼、柠条、梭梭、白皮沙拐枣 ;随植物年龄增长 ,蒸腾系数有上升的趋势 ,而蒸散系数有下降的趋势 ;在民勤沙区 6～ 9月是主要蒸腾季节 ,该时段的蒸腾量占全年蒸腾量的80 %～ 90 % ;植物的蒸腾量随年龄的增长而迅速增加 ,但增长幅度随物种不同而异。一般生长快的植物增长快 ,生长慢的植物增长慢。     

Protective effect of onychin on the human umbilical vein endothelial cells injured by menadione

AIM: To investigate the protective effect of onychin on the endothelial cells injured by oxidative stress. METHODS: The injured model was established by endothelial cells treated with menadione. The growth inhibitory rate of endothelial cell was determined by MTT assay; NO₂^-／NO₃^- concentration in the medium was determined by nitrate reductase assay; eNOS and caveolin-1 protein levels were determined by Western blot. RESULTS: Onychin significantly decreased the growth inhibitory rate of endothelial cells injured by menadione, increased NO₂^-／NO₃^- concentration in the medium and eNOS activity and up-regulated caveolin-1 expression. CONCLUSION: Onychin possesses a protective effect against endothelial cell injury induced by menadione via caveolin-1/eNOS pathway.     

Construction and identification of recombinant adenovirus vector containing CTLA4Ig gene

AIM:To construct a recombinant adenovirus expression vector containing CTLA4Ig gene.METHODS:The CTLA4Ig gene derived from the plasmid PCDNA3.0/CTLA4Ig by using polymerase chain reaction (PCR) was inserted into the backward position of cytomegalovirus (CMV) immediate early promoter of the shuttle plasmid (pAdTrack-CMV). After being identified by endonuclease, PCR and sequencing, the recombinant shuttle plasmid pAdTrack-CTLA4Ig was co-transformed into E.coli. BJ5183 cells with the adeoviral backbone plasmid pAdEasyl-1 to obtain the homologous recombination. The adenovirus was generated in 293 cells. A series methods such as PCR and fluorescence microscope was employed to identify the generated recombinant adenovirus.RESULTS:Recombinant CTLA4Ig adenoviruses were constructed and the titer of virus was generally up to 1.65×10¹² phaque forming units per liter (PFU/L).CONCLUSION:Success in constructing recombinant pAdTrack-CTLA4Ig will be the base of the further research on its expression in the mammalian cells, and be potenially used in the prevention of transplant rejection and autoimmunity diseases.     

Study on relationship between expression of PKCα in glomeruli and development of nephropathy in diabetic rats

AIM:To observe the dynamic changes of expression of PKCα, TGF-β₁ and α-SMA in glomeruli of diabetic rats induced by the alloxon and to invesitigate their roles in the diabetic nephropathy(DN).METHODS:Rats were randomly divided into four groups: normal control group (group A), diabetic group of one week (group B), diabetic group of one month (group C), diabetic group of two months (group D). Immunohistochemistry and Western blotting were used to detect the expression of PKCα, TGF-β₁ and α-SMA in renal tissue of all groups. Blood glucose, triglycerides, cholesterol, creatinine and urine protein were analysed by chemical methods. The morphological changes of renal tissue were checked through microscopy.RESULTS:The expression of PKCα and TGF-β₁ in renal tissue of diabetic groups were increased comparing with those of nomal control group(P<0.05). The mesangial cells expressed α-SMA in two months group. Chronologically the expression of PKCα, TGF-β₁ and α-SMA were positively correlative with each other and the impairment of kidney was also observed.CONCLUSIONS: During the DN process the expression of PKCα increased. PKCα raised GFR and the permeability of glomerular filtration membrane which enhanced urinary albumin excretion. PKCα also increased expression of TGF-β and therefore to induce the expression of α-SMA. The appearance of α-SMA was a marker of the phenotypic transform of renal cells.