小麦叶锈菌生理小种MFR的分子鉴定研究

 用AFLP方法对来自中国和墨西哥的23个小麦叶锈菌生理小种进行分析,共筛选了64对引物,获得一对引物(M₀₅/E₀₃)可在MFR小种中扩增出一条特异性DNA片段,进行回收、克隆、测序,结果表明该片段具有325个碱基。根据特异性片段序列设计出SCAR标记引物,对60个叶锈菌生理小种分离物进行回检结果表明,研制的SCAR标记能够准确区分MFR生理小种。本实验结果为小麦锈菌生理小种分子检测体系的建立奠定了基础     

基于GIS的中国小麦条锈病菌越夏区气候区划

 基于多年的气象数据(1980~2001年),首次从制约小麦条锈病菌越夏的温度因子入手,结合寄主小麦因素,利用地理信息系统(Geographical Information System,GIS),对我国小麦条锈病菌越夏区进行较详细的气候区划。本研究从温度条件上明确了全国适合小麦条锈病菌越夏的范围。研究表明,在我国小麦种植区适合小麦条锈病菌越夏的范围很广。其中甘肃、四川、云南、陕西境内适合越夏的地区是连成一片的,甘肃东部除了西边的几个县外其它地方7、8月份最高一旬均温在20~23℃,条锈病菌越夏困难;西藏、青海境内的小麦种植区几乎都适合小麦条锈病菌越夏;贵州境内适合越夏的地区可能和云南越夏区是一个整体。云南适合越夏的地区甚广,且地形复杂,需要进一步调查研究。     

菜豆新品种将军油豆的选育

将军油豆是以农家品种大马掌为母本 ,家雀蛋为父本人工杂交后系统选育而成。中熟 ,蔓生 ,从播种到采收 6 5d(天 ) ,生长势强 ,嫩荚绿色 ,扁条形 ,荚尖部有红条纹 ,平均荚长 2 0cm ,荚宽 2 .4cm ,单荚质量 2 4g ,纤维少 ,肉质面 ,属典型的东北优质油豆角类型。抗炭疽病、锈病 ,适应性广 ,春秋皆可种植 ,露地、保护地兼用     

棉花调亏灌溉的生理基础研究

以盆栽棉花为材料,通过苗期和现蕾期不同程度的亏水处理(低、中、高三个水平),对调亏灌溉节水效应及生理机制进行了研究。结果表明:适时适度的水分亏缺可使植株旺盛的营养生长得以有效控制,株型和根冠比都更为理想。调亏期间,蒸腾速率和气孔导度都明显下降,而光合速率下降不明显,复水后光合速率和气孔导度明显恢复且接近或高于对照;此外,水分亏缺不仅影响棉桃的数量,而且影响单果重。表明适度的亏水处理可使水分利用效率明显提高,而经济产量接近或高于对照,同时节水20%以上。     

体验经济与内蒙古草原旅游开发

本文通过捕捉近年来消费情况的变化 ,认为应对体验经济引起重视。在介绍体验经济的提出 ,体验的概念和体验的组成部分的基础上 ,提出体验经济对旅游具有创造差异化竞争优势、准确把握市场、使旅游者更舒适愉悦等意义 ,并在体验经济理论下结合内蒙古草原旅游的实际情况 ,提出内蒙古草原的体验设计和营销策略     

二棘血蜱叮咬中华硬蜱纯化抗原免疫接种宿主后的交叉免疫反应

选用中华硬蜱105kD柱层析纯化抗原对新西兰兔进行免疫接种,再用二棘血蜱进行叮咬,并与单纯二棘血蜱叮咬组和佐剂对照组进行对比,以探讨不同种属硬蜱之间的交叉免疫抗性。结果显示:单纯二棘血蜱叮咬组吸血量为181 3±44 3mg,而二棘血蜱叮咬由中华硬蜱105kD纯化抗原免疫接种组和佐剂对照组新西兰兔后其吸血量分别为102 1±25 3mg和168 5±40 9mg,纯化抗原免疫接种组较单纯二棘血蜱叮咬组和佐剂对照组吸血量分别下降43 7%和39 4%(P<0 01)。同时,纯化抗原免疫接种组也较单纯二棘血蜱叮咬组和佐剂对照组产卵量有显著下降。该研究结果表明中华硬蜱和二棘血蜱之间存在着交叉免疫反应。     

采收时间对蜡蚧轮枝菌分生孢子的萌发及致病力的影响

将蜡蚧轮枝菌Vp菌株在PDA培养基上23℃黑暗培养,分别于第5、15、20、25、30天后采收。将不同时间采收的分生孢子置于2％葡萄糖培养液内培养,16 h后检测其萌发率,结果表明,采收于第5天和第15天的分生孢子萌发率分别达到89.76％和94.98％,显著高于采收于第25天(30.27％)和第30天(6.12％)的孢子的萌发率;在PDA培养基培养5 d和15 d的分生孢子在相同浓度下对温室白粉虱的致病力分别达到83.40％和74.44％,显著高于培养了30 d的分生孢子的致病力(8.76％)。     

Effect of EGFP gene transfection on the cell cycle distribution of primary cultured human chondrocytes

AIM: To investigate the effect of enhanced green fluorescence protein (EGFP) gene transfection on the cell cycle distribution of primary cultured human chondrocytes in order to establish a tracking method of cultured human nasoseptal chondrocytes. METHODS: pEGFP-N1 plasmid was amplified in E.coli, and purified by high purity kit. Primary cultured human chondrocytes,which were initially obtained from the nasoseptal cartilage, were cultured in vitro and transferred with pEGFP-N1 by means of electroporation with Amaxa nucleofector device. Transfering process and transient expression were evaluated by laser scanning confocal microscope (LSCM), the transfer efficiency and the cell cycle distribution were evaluated by flow cytometry. RESULTS: There was significant expression of EGFP at 24 h after transferring. The transfection efficiency of pEGFP-N1 into primary cultured human chondrocytes reached 35.37％ at 48 h. It didn't affect the process of cell adherance and had no effect on the cell cycle distribution. CONCLUSION: Primary cultured human chondrocytes, which were transfected with pEGFP, are alive in vitro, and the transferring process doesn't affect the cell cycle distribution. These results suggest that pEGFP-N1 is an ideal transient expression vector for primary cultured human chondrocytes and it might be a well tracer in construction tissue engineered cartilage.     

Differential regulating effect on estrogen receptor α and β expression in female rat hippocampus and cortex regions between different types of estrogen regents

AIM: To study the regulatory effect two different estrogen reagents on expressions of estrogen receptor α and β in female rat hippocampus and cortex regions. METHODS: 12 cycles after ovariectomy, female rats were orally injected with premarin or progynova for 3 cycles before sacrificed. Semiquantitative RT-PCR was used to detect the ERs mRNA expression and SP immunohistochemistry was performed to measure the ERs protein distribution and expression. RESULTS: In premarin group, ER α mRNA levels in both hippocampus and cortex tissues decreased significantly compared with control. ER α protein level in hippocampus was lower than that in the control. However, ER α protein level in cortex had no statistical difference. ER β mRNA in the two regions and ER β protein in cortex had no statistical differences compared with control, while ER β protein level in hippocampus was higher than that in the control. In progynova group, both mRNA and protein levels of ER β increased significantly in the two regions compared with the control, and ER α mRNA level also increased in hippocampus, but ER α mRNA level in cortex and ER α protein levels in the above two regions showed no statistical differences. CONCLUSION: There were differential regulatory effects on ER α and ER β expression in female rat cognitive regions between the two different types of estrogen reagents, which may be one of the mechanisms of varied effects in different estrogen replacement therapy reagents.     

家鸡Leptin成熟肽cDNA的克隆、重组蛋白表达及纯化

从 18周龄鸡卵巢组织中抽提总 RNA,使用六聚体随机引物反转录后 ,用鸡 L eptin(瘦素 )特异性引物扩增出鸡L eptin编码区第 5 2～ 4 6 0 bp的长度为 4 0 9bp的 c DNA片段。根据鸡 L eptin的 3′端第 4 6 0～ 4 92 bp序列设计了 3条部分相互重叠并且顺序串联延伸的下游反义引物 ,并在最后 1条引物 3′端连接上 Eco R 切点 ;在以上用于反转录扩增的 5′端引物的 5′端连接一 Bam H 切点。用该 5′端引物分别与 3个 3′端引物配对 ,利用反转录扩增出的 4 0 9bp的L eptin c DNA片段作为第 1模板进行扩增 ,扩增产物再作为模板与下一引物对再次扩增。经 3次扩增得到编码鸡 L ep-tin成熟肽的全长 4 5 1bp的 c DNA序列。将该 4 5 1bp的 L eptin c DNA序列经 Bam H 和 Eco R 双酶切后 ,克隆入表达质粒 p RSET A的 Bam H 和 Eco R 两酶切位点之间 ,构建成表达质粒 p L ep- SCAU。转化有重组表达质粒 p L ep-SCAU的大肠杆菌 BL 2 1(DE3)在 L B培养基中培养后 ,经 IPTG诱导表达出相对分子质量为 2 0 10 0的鸡 L eptin融合蛋白和少量 4 0 2 0 0的 L eptin融合蛋白。L eptin融合蛋白的表达在 IPTG浓度为 0 .0 5 mmol/ L 时达到最高 ,占总菌体蛋白的 32 .6 %。用 Ni- NTA凝胶从 7L 发酵培养菌裂解液中纯化出 180 m g左右