欧洲鳗鲡淋巴细胞转化试验条件的建立

通过对培养时间、培养温度、刀豆蛋白A(ConA)质量浓度和鳗鲡血清质量分数4个参数的测定,确定欧洲鳗鲡(Anguilla anguilla)外周血淋巴细胞转化试验四甲基偶氮唑(MTT)法的实验条件。结果表明,在培养时间为42-90 h,培养温度分别为15.0℃、20.0℃、25.0℃和30.0℃时,细胞培养液中ConA质量浓度分别为0、10μg/mL、20μg/mL和30μg/mL,鳗鲡血清质量分数分别为0、5%、10%和15%时,淋巴细胞于20.0℃、含10μg/mL ConA,10%鳗鲡血清的RPM

Construction of Donor Plasmid in the Gene Integration Platform System for Oryza sativa L.

提高水稻产量，改良稻米品质是育种学家广泛研究的课题.随着现代生物技术的发展，水稻已成为植物基因工程的重要研究对象.许多实验室已成功地建立了一系列供外源基因转化水稻的系统.但是这些转化系统主要应用TI质粒衍生的载体，通过T-dnA左右两端的序列将目的基...Many laboratories have set up several foreign gene transformation systems for rice.But these transformation systems were all used T DNA system of Ti plasmid, then the foreign gene integrated into plant genomes DNA by means of the insertion of both ends of T DNA.The integrated target of T DNA in plant genome DNA is random, while the thoroughly random integration would interfere with self stable system of plant genome, which could lead to pernicious mutation.In this study, according to the mechanism of homologous recombination, we had constructed a new donor plasmid for indica rice.It would cause the foreign gene intergated into chromsomal rDNA locus. According to the known sequence of ribosomal DNA, we cloned the 2.5kb fragment of it by PCR, and used the fragment as the integrated homologous sequence.After subcloning foreign DNA including nptII gene and metallothionein gene at the end of homologous fragment, the donor plasmid pURKMT which will integrate into the genomes DNA of indica rice was constructed.Then, donor plasmid pURKMT was introduced into calli of indica rice (Jiahe NO.7) by electroporation.Screened by kanamycin, the transformant calli which was integrated the foreign DNA were selected.Dot blotting data showed that the foreign DNA including nptII gene and MT gene has integrated into rice genome DNA

A study on antioxidation of synechococcus sp. PCC 7942 withTrans-thymosin α1-gene in Mice

本试验室已在蓝藻聚球藻中高效表达了人源胸腺素α1(thymosinα1,Tα1)基因,为研究转Tα1基因聚球藻口服后的生物活性,本研究给小鼠灌服转Tα1基因聚球藻14d,研究其对小鼠谷胱甘肽过氧化物酶(GSH-Px)、过氧化氢酶(Cat)和超氧化物歧化酶(SOD)活力以及丙二醛(MDA)含量的影响,结果表明:转胸腺素α1基因聚球藻可显著提高小鼠心、肝与肾中GSH-Px活力(P<0.01);明显提高心脏Cat活性(P<0.01);显著降低肝脏中MDA的含量(P<0.01);但对SOD活力无明显作用。提示转胸腺素α1基因聚球藻较强的抗氧化作用。Human thymosin α1 gene was expressed effectively in Synechococcus sp. PCC 7942 and antioxidant effect of Synechococcus sp. PCC 7942 with trans-thymosin α1-gene in mice were investigated. Synechococcus sp. PCC 7942 with trans-thymosin al-gene were administrated orally 14d,Laters the results showed that the activities of glutathione peroxidase (GSH-Px) in heart、liver and kidney were increased significantly (P<0. 01);the activity of catalase (Cat) in heart was increased markedly;the content of malondialdehyde (MDA) in liver was decreased obviously (P<0.01). But no significant change in the activity of super-oxide dismutase (SOD) was observed. It indicated that Synechococcus sp. PCC 7942 with trans-thymosin α1-gene had obvious antioxidation in vivo.国家海洋863课题(项目编号:819-04-03);福建省自然科学基金项目(项目编号:c0010002

The Investigation Report on Current Status of Sports Consumption in Xiamen

通过对厦门市各阶层人士进行问卷调查 ,对体育经营企业的经营状况实地了解 ,分析厦门市体育消费现状。在 1998年厦门市家庭年均收入为 2 5 6 6 2元 ,年均体育消费为 75 4.95元。在体育消费种类上以体育物质产品消费为主 ,占消费总额的 6 5 .76 %。激发体育消费的因素主要有 :为了身体的健康、个人兴趣爱好等。影响体育消费的主要因素 :价格较高、没时间等。法人体育消费额达 10 0 0万元 (1998年 ) ,目前正呈良好的发展趋势。In order to investigate the sports consumption in xiamen, a total of 2000 questionnaire have been sent out with 1921 taken back. In 1998, the average family income per year is RMB 25662, while the average sports consumption is RMB 754.95. The expenditure on sports products is about the 65.76% of whole expense. The main factors for stimulating expenditure are for health, personal interests and hobbies. High prices and lack of time hamper people from consumption in Xiamen. Legal person sports consumption occupies a quite percentage and reaches 10 million

以课题式实验教学提高学生科研兴趣和科研能力的探索——以“遗传学实验”为例

传统的实验教学多为验证性实验,实验结果可预测且大同小异,缺乏新意和挑战,对于拔尖学生来说如同鸡肋,因此在经典传统的实验教学中进行内容改革,提高难度势在必行。本文以遗传学实验中的经典实验模式生物果蝇为例,开展了课题式实验教学改革,以果蝇诱变为命题,大大激发了学生的科研兴趣,同时拓展了科学思维,培养了科研能力,体现了研究性学习的创造性和挑战性,是生物学实验教学改革的有益探索。“基础学科拔尖学生培养计划”研究课题(20180214,20170606

p38MAPK induces apoptosis of glioma cell

目的　研究 p38MAPK基因转染大鼠胶质瘤细胞系C6后对其生物学特性的影响 .方法　利用脂质体介导法将p38MAPK基因导入大鼠胶质瘤细胞系 C6中 ,用免疫细胞化学染色检测其在细胞转染前后的表达情况 ,用 HE染色、流式细胞仪等方法研究其对细胞形态、粘着状况和生长周期的影响 .结果　转染 p CMV5 - p38MAPK质粒组 p38MAPK蛋白表达阳性 ,细胞形态发生变化 ,贴壁性降低 ,出现大量凋亡细胞 .结论　转染 p38MAPK基因可诱导胶质瘤细胞凋亡 【英文摘要】 AIM To study the effect of p38MAPK transfection on the biological characteristics of glioma cell C6. METHODS p38MAPK was transfected into glioma cell C6 by lipofectin. Expression of p38MAPK was detected by immunocytochemistry. HE staining and flow cytometry were adopted to measure the cell morphology, adhesion and cell cycle. RESULTS p38MAPK was expressed in transfected glioma cells, with cell biological characteristics changing and apoptotic cells emerging. CONCLUSION Apoptosis of glioma cell could be ...高等学校骨干教师计划资

在福建东南沿海局部地域献血员中检出HTLV-I

[目的 ]进一步阐明福建沿海 HTL V小流行区 HTL V- 的地理分布特点及毒株的基因类型。 [方法 ]对福建东南沿海莆田地区献血员以国产双抗原夹心法 EL ISA试剂筛选 ,对 EL ISA阳性血清用 Western blot(WB)进行确证。对抗体确证阳性者 ,采集外周血分离淋巴细胞用巢式 PCR扩增 HTL V- env区 gp46片段进行序列分析鉴定病毒亚型。 [结果 ]从 1998年 10月至 2 0 0 0年 4月止 ,共检测 45 6 4份标本 ,结果确证出 16例 HTL V- 抗体阳性者 ,感染率为 0 .35 %。HTL V- 抗体阳性者主要分布在某村献血人群中 ,并具有区域集中的特点。笏石秀屿一带某村献血员中感染率高达 4.7%。7例代表性毒株经病毒序列分析为 HTL V- C亚型 (COSMOPOL ITAN)。[结论 ]福建东南沿海某村献血员中发现 HTL V- 流行。提出在对某一地区人群进行 HTL V筛选时 ,既要注意整个地区“面”的筛查 ,又要注重某个村镇“点”的调查

Chemical constituents and cytotoxicity assay research in small polar substances from Vitis thunbergii var. taiwaniana

该文对小叶山葡萄地上部分化学成分进行了研究,运用硅胶柱色谱,OdS中低压柱色谱,SEPHAdEX lH-20凝胶柱色谱,分析型和制备型HPlC从小叶山葡萄60%乙醇提取物大孔树脂95%乙醇-水洗脱部位分离得到12个化合物,利用高分辨质谱,核磁共振等波谱手段鉴定其结构分别为:(1)bETulInIC ACId,(2)2,2,2'-bIS(4-HydrOXyPHEnyl)PrOPAnE bIS(2,3-EPOXyPrOPyl)ETHEr,(3)ErIOdICTyOl,(4)TrAnS-ε-VInIfErIn,(5)(+)-CIS-ε-VInIfErIn,(6)kObOPHEnOl A,(7)AMPElOPSIn A,(8)nEPAlEnHEnOl,(9)CIS-MIyAbEnOl C,(10)CIS-VITISIn b,(11)CIS-gnETIn H和(12)(+)-HOPEAPHEnOl。化合物2,5,6,8,9,10,11均为首次从为葡萄属中分离得到的化合物,化合物3,7,12为首次从小叶山葡萄中分离得到的化合物。在作用浓度为50μMOl·l-1下,化合物6,7和11对MCf-7(乳腺癌细胞株)具有较明显的体外生长抑制作用,其抑制率分别为66.58%,57.16%,52.84%。This article studied the chemical constituents from the aerial part of Vitis thunbergii var.taiwaniana.The 60% ethanol extract was eluted with 95% ethanol though HP-20 macroporous adsorption resin column.12 compounds,including( 1) betulinic acid,( 2) 2,2,2'-bis( 4-hydroxyphenyl) propane bis( 2,3-epoxypropyl) ether,( 3) eriodictyol,( 4) trans-ε-viniferin,( 5)( +)-cis-ε-viniferin,( 6) kobophenol A,( 7) ampelopsin A,( 8) nepalensinol B,( 9) cis-miyabenol C,( 10) cis-vitisin B,( 11) cis-gnetin H and( 12)( +)-hopeaphenol,were separated by using normal phase silica gel,ODS,Sephdadex LH-20 column chromatographies and semi-preparative or preparative HPLC.Compounds 2,5,6,8,9,10,11 were separated from the genus Vitis for the first time and compounds 3,7,12 were separated from Vitis thunbergii var.taiwaniana for the first time.At a concentration of 50 μmol·L-1,compound6,7 and 11 showed strong cytotoxicity against MCF-7 cell lines with the inhibition rate of 66.58%,57.16%,52.84%,respectively.国家自然科学基金青年基金项目(81202419

Preparation and determination of polyclonal antibody to thymosin α1

目的 :制备用于检测转胸腺素基因蓝藻表达产物的特异性抗体。方法 :用提纯的小肽 (2 8个氨基酸 )胸腺素α1与牛血清白蛋白偶联后作为抗原 ,采用皮下多点注射免疫的方法免疫大鼠。经过 3个月的免疫 ,获得抗Tα的多克隆抗体。结果 :用间接酶联免疫吸附 (ELISA)方法 ,测得抗体效价超过 40 96。蛋白印迹 (Westernblot)检测结果显示 ,该抗体能特异性地与胸腺素α1抗原产生明显免疫亲和反应。结论 :所制备的抗体具有很好的灵敏性和特异Objective:To prepare specific antibody against Thymosin α1 Methods:Thymosin α1(Tα1,28 peptide) was conjuncted with BSA as immune antigen,rats were immunized and the polycolonal antibody to Tα1 was obtained.Results:With ELISA detection,the titer of antibody was more than 1:4 096;Western blot analysis showed that the antibody can bind with Tα1 specifically.Conclusion:The prepared antibody against Tα1 has good specificity and reactivity and can be used to detect the expression products of transgenic cyanobacteria which expressed Tα1 gene.国家“863”课题资助!(No 819 0 4 0 3

p38MAPK induces apoptosis of glioma cell

目的　研究 p38MAPK基因转染大鼠胶质瘤细胞系C6后对其生物学特性的影响 .方法　利用脂质体介导法将p38MAPK基因导入大鼠胶质瘤细胞系 C6中 ,用免疫细胞化学染色检测其在细胞转染前后的表达情况 ,用 HE染色、流式细胞仪等方法研究其对细胞形态、粘着状况和生长周期的影响 .结果　转染 p CMV5 - p38MAPK质粒组 p38MAPK蛋白表达阳性 ,细胞形态发生变化 ,贴壁性降低 ,出现大量凋亡细胞 .结论　转染 p38MAPK基因可诱导胶质瘤细胞凋