马占相思扦插快繁育苗技术研究

通过双因素试验设计研究了3种不同木质化程度插穗(A)、4种不同浓度生根促进剂ABT-1#(B)和不同扦插基质(C)对马占相思扦插生根率、生根数及根长的影响差异,结果表明:未木质化的嫩枝(A1)+生根促进剂ABT-1#400 mg.kg-1(B2)生根率高、生根数多及生根长,生根率最高达83.3%;不同基质扦插中以未木质化的嫩枝(A1)+生根促进剂ABT-1#400 mg.kg-1(B2)+80%红心土和20%珍珠岩混合基质最佳。     

沙地彰武松容器育苗基质配比研究

在彰武松容器育苗过程中进行了育苗基质不同配比和不同施肥对比试验,结果表明,最适合彰武松容器苗高生长的基质配比草炭∶沙壤土∶三元素复合肥为1∶1∶0.05,其平均苗高为28.4 cm,方差分析表明各处理间差异极显著。     

奶牛乳腺上皮细胞三维培养的形态观察

利用原代培养后纯化的奶牛乳腺上皮细胞,以Matrigel为基质胶原,进行奶牛乳腺上皮细胞的三维培养,细胞接种浓度分别为1×104、1×105和1×106个细胞/mL。经过16d培养后,用DAPI对细胞染色,利用荧光显微镜观察细胞生长状况。结果表明,当细胞接种浓度为1×104～1×105个细胞/mL时,细胞形成了团块状结构,出现了类似腔状的腺泡形态。     

酵母基因表达调控关系的构建及其统计特性分析

[目的]从复杂网络的角度研究酵母细胞周期调控网络的统计特性。[方法]首先对酵母的细胞周期基因表达数据采用皮尔逊相关性度量,计算基因间的关联矩阵,即建立简单的基因调控网络;同时为了能够得到在宏观角度对大规模的基因调控有一个全貌的了解,进一步分析所建立调控网络的统计特性,通过计算所建立网络的统计特性：即计算网络的聚类系数、平均路径长度和网络的度分布。[结论]发现所建立的网络具有无标度和小世界特性,即所建立的酵母基因调控网络属于复杂网络,这为进一步深入研究基因调控网络的统计学和动力学特性打下了基础。     

基于Matlab的AHP分析程序设计

层次分析法是目前最为广泛应用的决策方法,但涉及大量的矩阵运算,影响了该方法的推广。Matlab软件精于矩阵运算,与C语言结构类似,移植性强,本研究基于Matlab设计出了便捷高效的AHP计算机程序。     

Simulation of pressure caused by multiplication and swelling of Erwinia amylovora in intercellular space of host tissue

WhenErwinia amylovora grows, in an intercellular space of a host, and fills this space, further multiplication or swelling may create a pressure, and may cause tearing of host tissue. Theoretically, this bacterial pressure equals the actual water potential of the host tissue minus the water potential at which the bacterial biomass would completely fill the intercellular space, but without exerting pressure.Simulation runs indicate that, when the pressure increases, the extracellular slime ofE. amylovora shrinks by releasing water, thus allowing further production of bacterial dry matter. The slime remains around the bacterial cells as a dense substance, low in water content, having a strong capacity to swell when the pressure induces tearing apart of the host tissue. Simulation runs show that the pressure attains its highest values at evening and night.Some fire blight symptoms that illustrate the evidence of bacterial pressure are discussed.     

腐蹄病节瘤拟杆菌的分子致病机制的研究进展

腐蹄病是反刍动物绵羊、山羊、鹿和奶牛等常见的一种高度接触性传染病。节瘤拟杆菌是致病作用的主要病菌之一,它是通过IV型纤毛和细胞外蛋白酶而产生作用。但从腐蹄病发病症状看,节瘤拟杆菌所致疾病的严重程度不是相同的,据此节瘤拟杆菌被分为毒性、弱毒性和良性菌,这种分类通过对该菌基因组毒性关联蛋白Vap(Virulence-associated protein)区域和毒性相关位点vrl(Virulence Related Locus)区域的研究,发现其致病特点与基因的顺序有很大联系。     

狂犬病病毒糖蛋白膜外区基因在大肠埃希氏菌中的高效表达

为获得狂犬病病毒（RV）糖蛋白抗原，采用RT-PCR方法从狂犬病病毒ERA株中扩增了编码RV糖蛋白的全长基因，将其克隆于pMD18-T载体，再经PCR扩增出糖蛋白全长基因和膜外区基因，将其分别亚克隆至原核表达载体pET-28a（＋）、pET-32a（＋）和pGEX-4T-1中，经PCR和双酶切鉴定以及序列分析，表明已成功构建了重组质粒。将重组质粒转化到大肠埃希氏菌BL21（DE3）中进行表达，结果显示，克隆到pET-32a（＋）的糖蛋白膜外区基因表达量最高，目的蛋白表达量占菌体总蛋白的45．4％。经Western-blotting检测，不同载体表达的糖蛋白膜外区产物均可与兔抗RV多抗发生特异性反应，表明，重组蛋白具有良好的反应原性。     

Estradiol stimulated proliferation and differentiation of prostatic stromal cells through regulation of BPH-1 paracrine

AIM: To characterize the effect of estradiol on proliferation, differentiation and extracellular matrix (ECM) accumulation in stromal cells through regulation of BPH-1 paracrine. METHODS: BPH-1 cells were stimulated with different concentrations of estradiol. Conditioned media (CM) were harvested and their effects on stromal cell cultures were tested. Cell proliferation was determined by MTT assay. mRNA of smoothelin, fibronectin, collagen Ⅳ and transforming growth factor β₁(TGF-β₁) were analyzed by real-time RT-PCR. Western blotting was used to determine smooth muscle myosin heavy chain (SMMHC). ELISA and radioimmunoassay were respectively used to measure fibronectin, TGF-β₁ and collagen Ⅳ protein expressions.RESULTS: Estrodiol stimulated the expression and secretion of TGF-β₁ in BPH-1 cells. The proliferation of stromal cells increased when they were cultured with CM harvested from estrogen treated BPH-1 cells. The mRNA levels of collagen Ⅳ and smoothelin increased in stromal cells treated with CM from BPH-1 cells. The results of radioimmunoassay also showed that the collagen Ⅳ protein level up-regulated in the supernatants and cell extracts of CM-treated stromal cells. A neutralizing antibody to TGF-β₁ inhibited the stimulation of collagen Ⅳ and SMMHC by BPH-1 CM. The expression of fibronectin was only marginally changed in stromal cells cultured in the presence of BPH-1 CM. CONCLUSION: The BPH-1 cells increase ECM accumulation and differentiation of stromal cells through TGF-β₁. Estradiol stimulate differentiation of stromal cells by induction of TGF-β₁ expression. Estradiol stimulate proliferation by influencing the factors secreted from prostatic epithelial cells.