重组逆转录病毒载体的包装

将3.7kb的LacZ基因片段克隆到含标志基因Neo的逆转录病毒载体，pLXSN与pLNCX的多克隆位点，构建了含有LacZ基因的重组逆转录病毒载体pLLSN和pLNCL.在测定了G418对饥装细胞系PA317的最小致剂量后（最小致死剂量为0.3g/L），通过脂质体Lipofectin与磷酸钙2种介质，分别将2种重组逆转录病毒载体导入包装细胞系PA317进行包装，并以0.3g/L，的G418进行筛选，得到多个G418抗性克隆，经扩大培养，传代，分别得到包装pLLSN与pLNCL的2株阳性细胞，电镜下可见阳性细胞的培养上清中具有逆转录病毒形态特征的成熟病毒粒子，本0研究为运用逆转录病毒载体系统，解决转角因效率低的问题奠定了基础。     

In vitro Plant Regeneration from the Mature Tissue of Navel Orange (Citrus sinensis L. Osbeck) by Direct Organogenesis

An efficient in vitro regeneration system by direct organogenesis from mature nodal and internodal stem segments of Newhall navel orange (Citrus sinensis L. Osbeck) was developed. Illuminating conditions together with plant growth regulators affected the adventitious bud regeneration frequency and efficiency. The initial 15 d darkness inoculation is beneficial for the adventitious bud regeneration. The highest regeneration frequency (85.2%) and bud formation efficiency (3.7 per responsive internodal stem segment) were obtained in the media supplemented with 1.0 mg L-1 BAP and 0.5 mg L-1 NAA. ABA at 0.2 mg L-1 positively affected the bud formation efficiency, which amounted to 8.5 buds per internodal segment in the presence of BAP at 1.0 mg L-1. The adventitious shoots successfully rooted and were transferred to the soil.     

鸡大肠杆菌病中草药佐剂多价灭活苗的研制——Ⅰ、疫苗生产工艺

采用鸡大肠杆菌多发病型菌株以及地方病型菌株作为制苗用菌种，保证了疫苗既具有一定的广谱性，又具有一定的特异性；采用液体通气培养方法，在一定程度上提高了菌数；采用中草药蜂胶作为佐剂不但可有效地提高机体的免疫功能，同时兼具有治疗，保健和促生长作用，另外蜂胶还可以增大抗原表面积，延长抗原在组织的贮存时间，可持久地释放抗原，保证了机体持续产生高效价抗体。     

垃圾浸出液厌氧处理研究

本研究采用厌氧—好氧生物氧化的工艺技术,自行设计和制造了一套有机玻璃为材料的模拟装置,对垃圾浸出液进行处理研究。经试验结果表明,利用本设计装置处理后的污水,可运到国家农田灌溉的污水排放指标并基本达到国家三类废水的排放指标。该成果已通过市级专家鉴定,并将应用于垃圾场淤出污水的处理工程。     

以CP23重组蛋白为抗原建立检测微小隐孢子虫抗体间接ELISA方法的研究

摘要：以在E.coli高效表达的微小隐孢子虫子孢子表面抗原CP23为抗原，以辣根过氧化物酶(HRP)标记的山羊抗鼠IgG为二抗，建立了检测微小隐孢子虫抗体的间接ELISA方法。经检测筛选出最佳反应条件为1μg／孔纯化的E.coli表达的CP23抗原包被酶标板，用10％免血清进行封闭，以正常E.coli裂解上清液稀释待检血清。实验表明应用CP23重组蛋白作为诊断C.parvum抗原具有特异性高、抗原易纯化和成本低等特点。     

宰前运输对肥育猪胴体、内脏及肉质的影响

本试验对 1 0头宰前运输应激的大长淮 (大白×长白×淮猪 )肥育猪 (试验组 )和5头宰前无应激的大长淮肥育猪 (对照组 )作了胴体、内脏及肉质测定。试验组与对照组在胴体性状和内脏重量 (心脏除外 )方面无显著差异。应激组和对照组的肌肉 p Hu和肉色评分分别为 5.50 ,2 .2 5和 5.88,3 .0 0 ,差异显著 (P<0 .0 1 )。试验组肉质有下降趋势。     

茯苓液体培养条件研究及其营养浓缩液的相关检测

研究表明，液体培养条件下，茯苓经0～48h的适应期，48～144h的增殖期后进入稳定期，发酵液pH骤降。经检测，发酵液中含有包括十六烷酸和十八烷酸在内的有机酸；发酵罐培养120h，生物量≥30g/l00mL(鲜重)。茯苓营养浓缩液多糖含量≥5．0mg/mL，氨基酸含量≥480mg/100mL。动物实验证明，茯苓营养浓缩液具有显著的抗疲劳和提高机体免疫力作用，其重金属和微生物指标均符合国家标准。     

番鸭在南京地区的适应性观察

番鸭在南京地区进行冬、夏两批饲养,均有较强的适应性。试验结果表明:冬、夏两 批饲养的番鸭只平均重量差异不显著(P>0．05)。夏季与冬季的料重比分别为1:2．62和1: 3．07,冬季饲养的鸭子饲料利用率低,料重比大于夏季。冬季在塑料大棚中饲养番鸭精饲料减 少1／3,添加青粗饲料能达到同样的增重效果。温度与增重无相关关系,相对湿度与番鸭的增 重呈负相关(P<0．01)。鸭舍内平均温度在11．05℃-30．93℃之间,相对湿度在76．28％以 下,番鸭能正常生长发育。环境温度在9．8℃以下,番鸭的生长发育受阻,饲料利用率降低。相 对湿度在77％以上,其增重受到影响。特别在低温高湿的环境中,严重地影响番鸭的生长。在 相同的饲养期内,周平均温度9．8℃,平均相对湿度91％,番鸭周平均增重22 g,周平均温度 27．42℃,平均相对湿度71．29％,番鸭周平均增重355 g,相差333 g(P<0．01)。     

Relation between TNF-α,TNFR I expression and apoptosis in oral lichen planus

AIM: To examine the expression and distribution of tumor necrosis factor-α (TNF-α), tumor necrosis factor receptor I (TNFR I) and apoptosis in oral lichen planus, and evaluate their roles and relation in the oral lichen. METHODS: Immunohistochemical technique and TUNEL were employed to study the expression of TNF-α, TNFR I and apoptosis in 50 cases of oral lichen planus and 10 normal oral mucosa specimens. RESULTS: Compared with the normal control group, TNF-α expression was upregulated in mononuclear cells in lamina propria and decreased in keratinocytes in oral lichen planus lesion (P<0.05). On the contrary, TNFR I expression was increased in keratinocytes and decreased in lamina propria in oral lichen planus lesion (P<0.05). The increased apoptosis index in keratinocytes and the decreased apoptosis index in lamina propria were found in oral lichen planus (P<0.05). CONCLUSION: The accelerated apoptosis of keratinocytes and the inhibition of lymphocytes apoptosis may contribute to the formation and progression of oral lichen planus.     

Chloride channels of platelets

Chloride channels distribute widely in the body, and participate in many physiological actions and regulatory processes. Based on their physiological roles and molecular structures, six kinds of chloride channels have been identified: (1) The chloride channels family; (2) Cystic fibrosis transmembrane conductance regulator; (3) Swelling-activated chloride channels; (4) Calcium-activated chloride channels; (5) The p64 (CLIC) gene family; (6) γ-aminobutyric acid and glycine receptors. The chloride channels do exist in platelets, and their appearances are dependent on the presence of intracellular calcium. Blocking agents of chloride channels inhibit the thrombin-activated platelet aggregation and the elevation of the intracellular calcium concentration in a dose-dependent manner. It is suggested that chloride channels play a role in the activation of platelets. In addition, chloride channels act on both the cell volume regulation and the intracellular pH regulation in platelets.