长期培肥对土壤酶活性的影响

25a的有机肥长期定位试验地中土壤养分和有关酶活性研究表明:耕种和不同的培肥方式均能提高土壤养分的含量,明显地改善土壤的生物活性,其中对土壤脲酶和磷酸酶活性影响明显,多酚氧化酶显著性则较差。对土壤酶活性进行相关分析发现,土壤脲酶和碱性磷酸酶之间呈极显著正相关,且这两种酶与有关主要土壤肥力因子均呈显著或极显著正相关关系。揭示出了土壤脲酶和碱性磷酸酶活性可以用来作为评价土壤肥力的综合指标。     

农田沙漠化演变中土壤质量的生物学特性变化

通过研究处于沙漠化过程中的科尔沁沙地旱作农田土壤酶活性与基础土壤呼吸活性，分析了土壤质量生物学特性的沙漠化演变。结果表明，土壤酶活性与基础土壤呼吸对沙漠过程中环境的变化反应敏感，随着沙漠化程度增加，与土壤物理化学肥力因素有关的过氧化氢酶、脲酶和碱性磷酸酶的活性和土壤呼吸活性随之下降。土壤酶活性和呼吸活性与土壤有机质和养分有极显著的相关，在一定程度上可以用酶活性和呼吸强度表征有机质和养分的状况及其数量的变异，因此，可以作为农田沙漠化演变中土壤质量特征变化的重要辅助指标。     

1-(1-苯基-1,2,4-三氮唑-3-氧代乙酰氧基)烃基膦酸酯的合成与植物生长调节活性

合成了一系列新的1-(1-苯基-1, 2, 4-三氮唑-3-氧代乙酰氧基) 烃基膦酸酯, 并测定了它们对小麦和黄瓜的植物生长调节活性。结果表明, 在100 Lg/g 时, 所有化合物对小麦芽鞘的生长具有抑制作用, 而在10 Lg/g时化合物6a、6g 对黄瓜显示了较高的促生长活性。     

新型取代氨基(或芳氧)磺酰基苯氧丙酸酯的合成及其除草活性

由α-苯氧基丙酸酯出发,合成了取代氨基(或芳氧)磺酰基苯氧丙酸酯,并测定了它们的除草活性。所有的化合物均经1H NMR和元素分析确证,初步的生测结果表明上述化合物具有一定的除草活性。     

镧素对镰刀菌Fusarium solani及其致病酶的影响

采用琼脂平板生长速率法及液体培养基培养测定了La对镰刀菌Fusarium solani的抑制作用和毒力,并测定了其对病菌胞外的果胶酶、蛋白酶和纤维素酶等几种致病酶活性的影响。结果表明,随着La2O3浓度升高,对病菌菌丝生长的抑制作用增强,对病菌的EC50和EC95分别为278.2和552.0 mg/L;在一定浓度范围内,La提高了单位量菌丝所产生3种致病酶的活性,但由于菌丝生长受到抑制,除蛋白酶外,病菌胞外致病酶果胶酶和纤维素酶的总量或总活性受到了抑制,降低了病菌的致病力。     

敌死虫对不同发育阶段烟粉虱的生物活性测定

敌死虫对烟粉虱成虫具有较强的驱避作用 ,99.1%敌死虫200、100、50倍液药后 2h～120h对黄瓜上烟粉虱的驱避率均在90%以上 ,50倍液处理药后3d的驱避率为98%～100%。药剂处理的非洲菊上烟粉虱成虫产卵量显著低于对照。敌死虫对烟粉虱卵具有一定活性 ,致死中量为10468.6mg/kg ;对若虫活性较高 ,对1、2、3龄若虫的致死中量分别为165.81、199.46、232.38mg/kg ,稀释倍数分别为5976、4968、4264倍。     

苏云金芽孢杆菌cry基因在大肠杆菌中表达产物和生物活性

研究了几种Bt cry基因于大肠杆菌(Escherichia coli)中表达产物在pH 10.0的50mmol/L碳酸钠和20mmol/L乙醇胺溶解液中的溶解性 ,发现同样的Cry蛋白在碳酸钠中的溶解度大于乙醇胺。通过胰蛋白酶消化 ,明确Cry1Ca7、Cry1Ia8酶解产物为 38kD多肽 ;Cry1Ie1、Cry1Cb2、Cry2Ab4酶解产物为 41kD多肽 ;Cry1Ac酶解产物为60kD多肽。采用FPLC层析方法对 6种原毒素及其酶解后得到的毒素多肽进行了分离纯化 ,比较了原毒素和毒素的杀虫活性的差异。其结果表明 ,Cry1Ac的原毒素和毒素对棉铃虫初孵幼虫的校正死亡率均为 100% ,Cry2Ab4的原毒素的毒力高于其酶解毒素。     

亚精胺对猕猴桃采后抗氧化酶活性的影响

 研究了不同亚精胺处理对猕猴桃采后抗氧化酶活性及保鲜效果的影响, 结果表明: 猕猴桃果实采后(8 ±2) ℃条件下贮藏12 d , SOD 活性达到高峰; POD、CAT、ASP 活性高峰相对SOD 推迟约13 d。不同亚精胺处理均不同程度地延缓了SOD 活性高峰的出现, 提高了SOD、CAT 的活性, 减少了MDA 的积累,降低了POD、ASP 的活性峰值, 延长了猕猴桃的贮藏保鲜期, 其中以Spd 与NAA 结合处理的效果最为显著。     

High efficient expression of human endostatin in E.coli and its antiangiogensis activity

AIM: To examine the expression of human endostatin in E.coli, produce its fusion protein antibody and observe its biological activity. METHODS: Endostatin gene was amplified by polymerase chain reaction,recombined with plasmid vector pGEX-2T and induced expression with IPTG.The protein activity was tested by endothelial cell proliferation inhibitory assay.Inclusion body crudely purified was used to generate polyclonal antibody to detect its expression at mouse's liver and kidney etc. RESULTS: The protein expressed was 20kD after digestion by thrombin,it appeared the anti-angiogenesis activity and Western blotting indicated the expression of endostatin in liver and kidney of mouse. CONCLUSION: The successful expression of human endostatin and the preparation of polycolonal antibody indicated its potential application in anti-angiogenesis therapy and diagnosis tumors.     

Effects of angiotensin II-induced hypertension chemotherapy on the activity of interleukin-1β converting enzyme in transplanted intracerebral rat gliomas

AIM: To investigate the activity of interleukin-1β converting enzyme in transplanted intracerebral rat gliomas under angiotensin II-induced hypertension chemotherapy. METHODS: The brain tumor model was produced in Wistar rats by stereotaxic inoculation of C6 glioma cells (1×10¹² /L). Tumor-bearing rats were treated with carmustine, teniposide and lisplatin (chemotherapy) during angiotensin II-induced hypertension. Then, the survival time of tumor-bearing rats, tumor blood flow, the concentration of drug, volume of gliomas and the activity of interleukin-1β converting enzyme in glioma were examined.RESULTS: The survival time of tumor-bearing rats was significantly longer in chemotherapy with angiotensin II-induced hypertension group than that of chemotherapy alone. In addition, regional tumor blood flow, the concentration of chemotherapeutic drug and the activity of interleukin -1β converting enzyme in transplanted rat gliomas were increased, while the volume of gliomas was decreased in hypertention chemotherapy group compared with chemotherapy alone. CONCLUSION: Chemotherapy with angiotensin II-induced hypertension has a enhancing effect on chemotherapy for improving the drug delivery to tumor tissue by a increased tumor blood flow and enhancing activity of interleukin -1β converting enzyme.