剡溪山水文化旅游资源开发设想

文化底蕴越是丰厚的旅游资源，开发价值就越高。正是众多文人贤士游剡访古，使浙东剡溪的历史、文化与自然山水完美地结合在一起，形成了绚丽多彩的剡溪山水文化。文化被认为是旅游业的灵魂，是一种潜在的旅游产品。要提高山水旅游产品的文化品位，必须将山水文化的潜在价值转化为旅游产品。本文对剡溪山水文化旅游资源的开发提出了以下设想：再现“唐诗之路”山水旅游美景，并着重于按唐诗及有关文献、传说等增添新景点，沿江、沿山、于水中进行山水、文化全面开发，形成立体式、全景式的剡中山水文化游道；可开发出文化生态、修学、科考、宗教、节庆等剡溪山水文化旅游产品。     

Detection,cloning and expression of bone morphogenetic protein-1 from human osteosarcoma cell lines

AIM:To manufacture recombinant protein of the highly conserved domain in human bone morphogenetic protein-1(BMP-1) using gene engineering methods as antigen for making wide spectrum antibody to BMP-1.METHODS:We analyzed the gene sequences and protein structures of BMP-1 and its related proteins, and chose a highly conserved fragment as target gene. Total RNA was prepared from human osteosarcoma cell line Saos-2, then the target gene was amplified with RT-PCR. The PCR product was cloned into prokaryotic expression vector pMAL c2 to get recombinant vector BMP-1(322-588aa)-pMAL c2. After transforming the recombinant plasmid into DH5-alpha and screening, several prositive clones were got for sequencing. Finally the transformed cells was induced with IPTG to get fusion protein.RESULTS:The BMP-1 gene fragment was successfully cloned into vector pMAL c2, and was able to express efficiently with IPTG inducement. The amount of expressed fusion protein is about 66%-72% in total volume of bacterial proteins.CONCLUSIONS:The recombinant protein contains several key domains(2 CUB domains and 1 EGF domain), which are shared by BMP-1 and its related proteins. Specific wide spectrum antibody to human BMP-1 and its related proteins may be generated with this recombinant protein antigen.     

Effect of antifibrotic herb serum on rat hepatic stellate cell proliferation and collagen synthesis

AIM: To investigate the effect of Chinese herbs, Ganxianfang(GXF), on rat hepatic stellate cells (HSC) proliferation and collagen synthesis. METHODS: Two types of herb serum, portal venous serum and circumferential venous serum, were prepared from rats infused intragastrically with 16, 8, 4 times adult dose of GXF decoction. HSC isolated from rat liver were processed with the above sera in vitro. Then we mensurated the radioactivity of HSC admixed with [[³H]H]proline and [[³H]H]thymine to judge the effect on proliferation and collagen synthesis of HSC. RESULTS: Both two types of serum collected 0.5, 1, 2 h after intragastrical infusion inhibited HSC proliferation (P＜0.05), and the serum collected 1 h after intragastrical infusion had the strongest effect (P＜0.05). Portal serum decreasea collagen synthesis (P＜0.05), but circumferential serum had no effect (P＞0.05). CONCLUSION: Inhibition of HSC proliferation and decrease of collagen synthesis may contribute to the GXF antifibrotic action.     

咯菌腈对草莓灰霉病Botrytis cinerea的毒力及防效研究初报

用生长速率法测定了咯菌腈、多菌灵、硫菌·霉威、苯醚甲环唑4种药剂对草莓灰霉病Botrytis cinerea的毒力。结果表明,4种药剂对草莓灰霉菌菌丝的生长都有不同程度的抑制作用,随药剂浓度增加抑制作用增强,其EC50值分别为0.0472、95.7193、0.4854、1.3611 mg/L,其中咯菌腈的毒力最强。田间防治试验结果表明:2.5%咯菌腈FC每667 m2施药量120 mL时防效为83.7%,80 mL时防效为67.7%;65%硫菌·霉威WP每667m2施药量100 g时防效为65.3%。     

Inhibitory effect of berberine on the activation and proliferation of T lymphocytes

AIM: To investigate the effect of berberine (Ber) on the activation and proliferation of T lymphocytes and its mechanism of action. METHODS: Whole peripheral blood from normal subjects was stimulated with phytohemagglutinin (PHA) or phorbol ester (PDB) plus ionomycin (Ion) and the expression levels of CD69 and CD25 were evaluated with flow cytometry after the staining with appropriate fluorescent monoclonal antibody. The distribution of cell cycles was analyzed by propidium iodide staining and dead cells by 7-aminoactinomycin live staining. RESULTS: 100 μmol/L and 50 μmol/L of Ber had significant inhibition of the expression of CD69 on T cells stimulated with PDB plus Ion or PHA, while effect of 25 μmol/L Ber was not significant. And as time of action extended, the extent of inhibition decreased. For the expression of CD25, Ber at the concentrations as above all exerted significant inhibitory effect in a dose-dependent manner. Moreover, Ber could block lymphocytes cell cycle progression from G₀/G₁ phase to S and G₂/M phase without phase specificity. Besides, live staining analysis revealed that Ber did not have significant cytotoxicity on lymphocytes. CONCLUSIONS: Ber significantly inhibits the expression of early and mid activation antigens of T cells and also blocks the progression of lymphocytes cell cycles. These results suggest that Ber exerts immunosuppression effect through inhibiting the activation and proliferation of T cells.     

昆虫病原线虫rDNA多态性分析

本文对国内外昆虫病原线虫斯氏属和异小杆属的47个品系进行rDNA—ITS PCR—RFLP分析，研究其DNA多态性，并构建了分子系统发育树状图。各品系的ITS区无明显的长度差异，PCR—RFLP分析将47个品系分为斯氏属和异小杆属两大类，两属线虫又分别分为11组和4组。所得结果丰富了ITS PCR—RFLP图谱库，为弄清我国的昆虫病原线虫与国外种类的分子系统发育关系及未定名线虫的鉴定提供重要依据，同时为筛选适合的线虫种类防治害虫奠定基础。     

肉仔鸡生长过程中行为与产热的变化

研究肉仔鸡成长过程中行为变化对产热量的影响 ,将 2日龄肉仔鸡 36只分为自由摄食、 50 %摄食和绝食 3组进行观测。立位行为集中在明期 ,特别是摄食 30min前后 ,暗期几乎没有出现立体行为。 2日龄时 ,每天约有 70 0min是立位的 ,其后 ,随着日龄的增加而减少。在自由采食区 ,公雏比母雏摄食时间长。 50 %摄食区较自由采食区的摄食时间少。在绝食区 ,随着日龄的增加 ,公母的立位时间呈现减少倾向。 2 1日龄之前随着日龄的增加其摄食时间也增加 ,其后呈现相反倾向。产热 (HP ,kJ/kg0 75)与摄食时间有相同倾向。在 2 1日龄前公雏的HP比母雏低 ,2 1日龄后母雏比公雏低。 1天中各个区的HP活动规律是摄食后 1h内最高 ,暗期降低 ;限制摄食量后 ,HP降低 ,明期和暗期的HP差也随之减小     

徐州地区烟粉虱发生规律及治理措施初探

通过近2a观察表明,徐州地区烟粉虱在田间消长大致分4个阶段,成虫有4个主要迁移期;其喜干热、耐高湿的生活习性、冬季保护地栽培面积的扩大、外来虫源的传入及防治不力是烟粉虱种群数量累积并引起暴发的主要原因;主要寄主有9科20余种栽培作物;寄主植株上虫量垂直分布:棉花上部>中部>下部,温室蔬菜一般中、下部>上部。可采取严格检疫、清洁田园、轮作换茬、黄板诱杀、覆盖防虫网、保护和利用天敌、药剂防治等措施进行治理。     

内生拮抗枯草芽孢杆菌BS-2菌株的发酵条件

内生拮抗细菌BS 2菌株在以黄豆粉为原料的 3号培养基中生长速度快 ,发酵滤液对辣椒炭疽病菌的抑制作用强 ,菌液对辣椒果炭疽病的防效最好。培养基初始 pH值、培养时间、温度、通气量等对菌株生长及其抗菌物质的分泌有明显影响。结果表明 ,以黄豆粉培养基、初始 pH值 6 .7(灭菌后 )、2 8℃、培养 4 8h、并尽量增大培养通气量 ,为菌株的最佳发酵条件。     

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.