VPAC2在CHO细胞的表达及鉴定

PAC2是垂体腺苷酸环化酶激活多肽(Pituitary adenylate cyclase activating polypeptide,PACAP)和血管活性肠肽(vasoactive intestinal peptide,VIP)的共同受体,介导多种重要生物学功能。为获得稳定特异表达VPAC2的中国仓鼠卵巢(Chinesehamsterovary,CHO)细胞,将pcDNA-VPAC2表达载体转染CHO细胞,G418筛选转染阳性克隆,PACAP38标准品诱导阳性克隆细胞的胞内cAMP生成,筛选出对PACAP38最为敏感的阳性单克隆细胞株(VPAC2-CHO),运用RT-PCR、Westernblot和免疫荧光法检测VPAC2受体表达情况,利用VPAC2受体特异激动剂通过竞争性结合试验和促进胞内第二信使cAMP生成的活性检测实验证实,VPAC2-CHO特异表达有功能的VPAC2。Scatchard作图分析显示VPAC2-CHO的VPAC2受体密度为(1.1±0.2)pmol/mg膜蛋白,PACAP38与VPAC2的解离常数Kd值为(0.55±0.10)nmol/L。特异表达VPAC2受体细胞系的构建为深入研究该受体理化性质、生物学功能以及筛选、开发VPAC2受体新型特异激动剂和拮抗剂等研究奠定了基础。     

深圳红树林区浮游植物时空变化与水质要素的关系

在探讨深圳福田红树林区浮游植物群落结构及种群数量变化规律的基础上,对红树林区不同水质环境中浮游植物时空变化进行了研究,初步分析主要水质因子与浮游植物密度时空变化的相关关系。分析表明,福田红树林区浮游植物有5门28属51种(含未知9种),以硅藻门种类为主,优势种为微小小环藻(Cyclotella caspia)和诺氏海链藻(Thalassiosira nordenskiöldi)等,蓝藻、绿藻能发展成为优势类群,优势种为小颤藻(Oscillatoria minima)和小球藻(Chlorella vulgaris)等。浮游植物种类组成季节变化明显,空间变化显著。浮游植物密度空间变化明显,季节差异不大。各季度的浮游植物密度较高,达到106cells·L^-1的级别。由于接纳生活污水、工业废水、养殖废水等陆源污水,5个站位的主要水质因子受污水排放影响明显,站位受陆源污水影响的顺序依次为:Ⅳ>Ⅱ>Ⅴ>Ⅰ>Ⅲ,污水排放进入红树林区的水域水质显著区别于完全海水水域。陆源污水输入对浮游植物密度时空变化造成显著影响,浮游植物密度与总氮浓度、盐度相关性较好,与总氮成显著负相关,与盐度成显著正相关。     

栅藻对水环境中镍的累积效应与机理分析

对不同Scenedesmus品种的藻细胞从含镍水溶液 (10mg/L)中累积金属镍的能力进行了分析 ,结果表明 :藻细胞对镍的生物累积量表现出明显的品种差异性。ScenedesmusquadricaudaFACHB 4 4和ScenedesmusquadricaudaFACHB 5 0 6表现出很强的累积能力 (累积量达到 5～ 6mgNi /g干重 ) ,而Scenedesmussp .FACHB 4 16和Scenedesmussp .FACHB 4 89在相同条件对金属镍累积量要少得多 (1～ 1.5mgNi /g干重 )。这种差异可能与不同品种藻细胞间的形态结构和生理特性是相关的。对S .quadricaudaFACHB 4 4重金属抗性和累积能力进一步的分析表明 ,S .quadricaudaFACHB 4 4用于含镍重金属废水处理是非常有效的 ,在高浓度 (10 0mg/L)的镍溶液中 ,藻细胞的最大累积量能达到 (2 6 .7mgNi/g干重 )。对该藻细胞镍累积动力学分析发现 :藻细胞对镍的生物累积包括一个快速的被动吸附过程 (5min ,结合 70 %的镍 )和一个缓慢的耗能累积过程 (2～ 3h时间内的累积量占总量的 2 0 %～ 30 % )。与其他藻类相比 ,S .quadricaudaFACHB 4 4对水溶液中镍的耗能累积量明显高于其他藻类。透射电子显微镜(TEM)和X射线能谱 (EDX)分析结果均表明 ,藻细胞耗能累积的镍主要集中在原生质体中 ,尤以淀粉粒和染色质中为多。     

Prunus necrotic ringspot virus isolates in stone fruit germplasm accessions and cultivars in Israel

Prunus necrotic ringspot virus (PNRSV) was detected in almonds, plum and apricot germplasm accessions and local almond cultivars in Israel. PNRSV was widespread both in wild and cultivated almond trees and uncommon in wild apricots and plums. The possible variation among the PNRSV isolates was initially evaluated by restriction analysis of PCR products representing the CP gene with the endonuclease RsaI and followed by nucleotide sequence analysis of selected isolates. It was concluded that all 13 isolates belong to group PV96, the largest cluster of PNRSV isolates, described previously. Two PNRSV isolates, one from a plum accession and one from an almond cultivar, were found to be distinct members of group PV96 with unique nucleotide modifications not found in other documented isolates of this virus. However, no PNRSV isolate typical to a specific host and/or to the Middle East region could be identified. This study expands the body of data on variability of PNRSV isolates and highlights the importance of assessing the virus status of germplasm collections by applying reliable diagnostic and differentiating methods.     

重组环状胸腺五肽结构类似物Cyclo-（Cys- Arg-Lys –Asp-Val-Tyr）的制备、鉴定和活性检测

为了实现蛋白内含肽(Intein)介导的重组环状胸腺五肽结构类似物［cyclo-（Cys -Arg-Lys –Asp-Val-Tyr）,cTP］的高效制备,设计并合成编码6个氨基酸的cTP基因,克隆到表达载体pTWIN1,重组表达质粒pTW-cTp转化E.coli ER2566构建工程菌,IPTG诱导由几丁质结合域纯化标签（chitin binding domain,CBD）、2个蛋白内含肽和目的多肽组成的“多元”融合蛋白(CBD-intein1-cTP-intein2-CBD)的高效表达.几丁质柱亲合层析纯化融合蛋白后,改变pH值和温度诱导intein1 C端切割,硫醇MESNA诱导intein2 N端切割,释放N端为Cys,C端为硫酯的重组cTP线性前体,通过非保护多肽硫酯环合法实现环肽生成.激光飞行质谱结果显示,纯化产物的分子量为764.4,与环肽的理论值相符.免疫活性检测结果显示,环肽cTP较线性多肽TP-5具有更显著的促进巨噬细胞吞噬能力的活性（P<0.01）和促进B细胞抗体生成的活性（P<0.01）.     

Structure of the Phytoplankton Community and Its Relationship to Water Quality in Donghu Lake, Wuhan, China

The phytoplankton community structure, in terms of species composition, total standing crop,and abundance of the dominant algal species, at four stations in Donghu Lake, Wuhan, China, was investigated monthly from January 1994 to December 1996. A total of 260 taxa was observed, of which Chlorophyta (106 taxa) contributed the highest portion of the total number of taxa, followed by Bacillariophyta (82 taxa) and Cyanophyta (32 taxa). The total standing crop measured by means of chlorophyll a content, cell density,and cell biovolume, as well as the abundance of the dominant species, declined in the order of Station I to Station IV. Seasonal changes of the standing crop varied greatly among the four stations. Although the cell density at the four stations showed a single peak within a year, the peak density varied from July to November, dependent on the sampling year and the station. For chlorophyll a content and cell biovolume,multiple peaks were observed at Stations I and II, but a single peak was found at Stations III and IV. The phytoplankton community structure indicated that the trophic status was the highest at Station I (most eutrophic), followed by Station II; Stations III and IV were the least trophic areas. The long-term changes in phytoplankton community structure further suggested that changes in phytoplankton community structure were correlated with water quality, and eutrophication of Donghu Lake had been aggravated since the 1950s.     

Typing Primus necrotic ringspot virus isolates by serology and restriction endonuclease analysis of PCR products

Primus necrotic ringspot virus (PNRSV) isolates were characterised by bioassays, serotyping and restriction fragment length polymorphism (RFLP) analysis of PCR products. Based on symptoms in host trees and bioassays it was concluded that only one of the 16 tested isolates is severe. The serotyping results demonstrated that by using four different MAbs in TAS-ELISA the tested isolates could be divided into four subgroups, however, the severe isolate could not be singled out. RFLP analysis of PCR products supported the serotyping data but did not differentiate between isolates of the two main serological subgroups. A restriction map, derived from sequence analysis of the PCR products obtained from selected isolates, allowed exact location of the restriction sites within the PCR products of each isolate. A mild isolate with a unique genome structure was identified by both serological and RFLP assays. As far as we are aware, this is the first report on sub-grouping of PNRSV isolates by bioassays, serotyping with MAbs and RFLP analysis.