漂浮植物修复技术净化城市河湖水体试验研究   总被引：7，自引：1，他引：6  

黄廷林  戴栋超  王震  解岳  钟建红 《地理科学进展》2006,25(6):62-67

阐述了漂浮栽培植物修复系统的技术原理、特点与系统组成, 研究了在该系统中种植美人 蕉和旱伞草2 种植物的生长状况以及这些植物对城市河湖水体中氮、磷等的净化效果。尝试了将 漂浮栽培植物与生物接触氧化技术结合起来, 并研究了植物与生物填料的组合系统对水质的改 善效果。结果表明, 美人蕉和风车草在漂浮植物修复系统对氨氮的去除率均在90%以上, 漂浮栽 培植物与软性填料的组合系统对水中COD_Mn 的去除率达46%以上。  相似文献   

Similarity of electrophoretic dissolved protein spectra from coastal to pelagic seawaters     

Namiha Yamada  Eiichiro Tanoue 《Journal of Oceanography》2009,65(2):223-233

Dissolved proteins in seawater samples collected from a coastal area of Tokyo Bay, Sagami Bay and a location off the Kuroshio Current were investigated by one-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and high resolution two-dimensional electrophoresis (2-DE). Four to nine protein bands were detected in SDS-PAGE in the apparent molecular weight (MW) range from 12 kilo Dalton (kDa) to 49 kDa. The 2-DE technique distinguished 10 to 46 protein spots exhibiting isoelectric point (pI)/MW ranging 4.3–9.2/12–63 kDa. The elecrophoretic patterns were similar between the coastal and pelagic samples, as well as previously reported patterns from various pelagic areas. The close similarity of electrophoretic mobility on both SDS-PAGE and 2-DE gels indicates the compositional homogeneity of dissolved proteins in seawater throughout a broad range of marine environments. Proteinaceous dissolved organic matter (DOM) that was unresolved and smeared staining characteristics on both SDS-PAGE and 2-DE gels was first observed in Tokyo Bay waters in the present study and its possible sources are discussed. Although the two protein species, 48 kDa and 39 kDa proteins, have been identified as homologues of Porin P and low molecular weight-alkaline phosphatase of Pseudomonas aeruginosa PAO1, respectively, four strains of P. aeruginosa and two species of Pseudomonas spp. have been newly identified as the source organisms of these proteins using the N-terminal amino acid sequence data determined in previous studies.  相似文献   

单环刺螠纤溶酶的分离纯化及其性质的初步研究   总被引：3，自引：1，他引：2  

郭金明  韩宝芹  刘万顺  初金鑫  蒋仲青  朱琦 《中国海洋大学学报(自然科学版)》2008,38(6)

从单环刺中制得单一组分的纤溶活性纤溶酶,并对其性质进行初步研究.单环刺体组织液经离心,超滤,离子交换层析,凝胶过滤等方法进行分离纯化,制得单一洗脱峰酶组分,经Native-PAGE电泳分析,SDS-PAGE电泳分析和飞行质谱分析,鉴定了酶制品纯度和相对分子量,进行了体外溶血栓试验.所得纯品UFEIa水解酪蛋白的比活力为442.0 U/mg,纯化倍数为12.1倍,回收率为27.0%.UFEIa为单一组分,相对分子量约23 800 Da.体外溶血栓实验表明此纤溶活性蛋白酶与蚓激酶相比具有很好的溶血栓活性.  相似文献   

大豆蛋白废水处理中泡沫分离过程的数学模型     

杨向平  刘元东  席作家  翟绪丽 《中国海洋大学学报(自然科学版)》2008,38(1):111-115

假设吸附过程始终处于平衡态、气泡大小均一以及每一个气泡均为正十二面体,构建了泡沫分离过程的数学模型.模拟了液池中蛋白质在气液界面上的吸附过程和泡沫层中气泡的失水过程,得出了富集比的表达式,可用于分离效果的预测.经验证,模型与实验条件下的泡沫分离过程基本符合.  相似文献   

Cloning and sequence analysis of a full-length cDNA of SmPPlcb encoding turbot protein phosphatase 1 beta catalytic subunit     

亓飞  郭华荣  王建 《中国海洋湖沼学报》2008,26(1):54-61

Reversible protein phosphorylation, catalyzed by protein kinases and phosphatases, is an important and versatile mechanism by which eukaryotic cells regulate almost all the signaling processes. Protein phosphatase 1 （PP1） is the first and well-characterized member of the protein serine/threonine phosphatase family. In the present study, a full-length cDNA encoding the beta isoform of the catalytic subunit of protein phosphatase l（PPlcb）, was for the first time isolated and sequenced from the skin tissue of flatfish turbot Scophthalmus maximus, designated SmPPlcb, by the rapid amplification of cDNA ends （RACE） technique. The cDNA sequence of SmPPlcb we obtained contains a 984 bp open reading frame （ORF）, flanked by a complete 39 bp 5＇ untranslated region and 462 bp 3＇ untranslated region. The ORF encodes a putative 327 amino acid protein, and the N-terminal section of this protein is highly acidic, Met-Ala-Glu-Gly-Glu-Leu-Asp-Val-Asp, a common feature for PP1 catalytic subunit but absent in protein phosphatase 2B （PP2B）. And its calculated molecular mass is 37 193 Da and pI 5.8. Sequence analysis indicated that, SmPPlcb is extremely conserved in both amino acid and nucleotide acid levels compared with the PPlcb of other vertebrates and invertebrates, and its Kozak motif contained in the 5＇UTR around ATG start codon is GXXAXXGXXATGG, which is different from mammalian in two positions A6 and G3, indicating the possibility of different initiation of translation in turbot, and also the 3＇UTR of SmPPlcb is highly diverse in the sequence similarity and length compared with other animals, especially zebraf＇lsh. The cloning and sequencing of SmPPlcb gene lays a good foundation for the future work on the biological functions of PP1 in the flatfish turbot.  相似文献   

White spot syndrome virus envelope protein VP124 involved in the virus infection     

ZHU Yanbing  WU Chenglin  YANG Feng 《海洋学报(英文版)》2008,27(4):130-136

White spot syndrome virus （WSSV） is one of the major shrimp pathogens causing large economic losses to shrimp farming. In an attempt to identify the envelope proteins involved in the virus infection, purified WSSV virions were mixed with three antisera against WSSV envelope proteins （VP39, VP124 and VP187 ）, individually. And then they were injected intramuscularly into crayfish （Procambarus clarkii） to conduct in vivo neutralization assays. The results showed that for groups injected with virions only and groups injected with the mixture of virions and antiserum against VP124, the crayfish mortalities were 100% and 60% on the 8th day postinfection, individually. The virus infection could be delayed or neutralized by antibody against the envelope protein VP124. Quantitative PCR was used to further investigate the influence of three antisera described above on the virus infection. The results showed that the antiserum against VP124 could restrain the propagation of WSSV in crayfish. All of the results suggested that the viral envelope protein VP124 played a role in WSSV infection.  相似文献   

Research on purification and modification of I/S bentonite     

Deli YU  Shufeng LIU  Liyu TIAN  Peiping ZHANG 《世界地质(英文版)》2008,11(3)

Analyzing raw material's structure and performance of bentonite from Panzhihua in Sichuan, the authors think that it is adequate for agglomerant of iron smelting. According to its composition and property we have researched the purification and modification of I/S bentonite under conditions of different dispersants and sodium agent. XRD test result reveals that the essential minerals of Panzhihua bentonite are I/S mixed-layer ones, and FTIR analysis shows that when adding 1 5% sodium pyrophosphate to the bentonite slurry during purification, the composition of quartz in bentonite decreases to less than 4% and I/S is more than 90%. The optimized modification technic conditions are Na2CO3 (4%) and CMC-Na (3%) as modified agents, the clay and water are 10 vs. 1, and the temperature is 75℃. It is 40 min for stirring time and reacting time is 4 h. Under the conditions we can get the modified I/S bentonite with colloid index more than 500 ml/15 g.  相似文献   

黄斑篮子鱼去毒相关基因的克隆与肝脏组成型表达分析   总被引：1，自引：0，他引：1  

王琳  梁旭方  林群  李光照  胡永乐 《热带海洋学报》2009,28(6):79-87

从基因水平探讨海洋鱼类对海洋藻毒素的去毒分子机理。采用RT-PCR法成功克隆了黄斑篮子鱼Siganus oramin肝脏I时相代谢酶细胞色素P450 1A(CYP1A)、II时相代谢酶alpha型谷胱甘肽S-转移酶(GSTA)和rho型谷胱甘肽S-转移酶(GSTR)、热休克蛋白70 (HSP70)、alpha 1型钠钾ATP酶(ATP1A1)及β-肌动蛋白(beta-actin, ACT)基因cDNA核心序列，序列分别长879 bp、582 bp、588 bp、660 bp、749 bp和554 bp。序列同源性分析发现，属鲈形目的黄斑篮子鱼CYP1A、GSTA和GSTR与同属鲈形目的牙鲆Paralichthys olivaceus、欧洲鲽Pleuronectes platessa、真鲷Pagrus major、鲤形目的斑马鱼Brachydanio rerio 相应氨基酸序列同源性较高，CYP1A和GSTA与非洲爪蟾(两栖类)、鸡(鸟类)、小鼠、大鼠和人(哺乳类)相应氨基酸序列同源性低，这可能与鱼类I、II时相去毒酶基因承担水环境毒素去毒代谢的特殊功能有关；而HSP70、ATP1A和β-肌动蛋白在鱼类、两栖类、鸟类、哺乳类中均有较高的同源性，这可能与这些基因在机体中承担的最基本的生命功能相关。应用半定量RT-PCR的方法，以β-肌动蛋白作为外参照，在指数期增长范围内分别得到了CYP1A、GSTA、GSTR、HSP70和ATP1A1 mRNA与β-肌动蛋白mRNA (%)的比值，确定黄斑篮子鱼肝脏去毒相关基因的组成型表达水平。其中，黄斑篮子鱼肝脏CYP1A、GSTA和GSTR基因组成型表达相对较高，HSP70和ATP1A1基因组成型表达相对较低，这可能与不同基因在黄斑篮子鱼海洋藻毒素去毒分子机理中承担的作用相关，为海洋藻毒素在海洋鱼类中的积聚及代谢去毒分子机制的研究提供了相关数据。  相似文献   

6种海洋致病性弧菌36kDa外膜蛋白特性分析   总被引：3，自引：0，他引：3  

唐小千  战文斌  周丽  绳秀珍 《中国海洋大学学报(自然科学版)》2009,39(2)

研究本着筛选和制备弧菌共同外膜蛋白亚单位疫苗,用十二烷基肌氨酸钠抽提并结合超速离心的方法提取了鳗弧菌(Vibrio anguillarum)、鱼肠道弧菌(V.ichthyoenteri)、溶藻弧菌(V.alginolyticus)、副溶血弧菌(V.parahaemolyticus)、哈维氏弧菌(V.harveyi)和创伤弧菌(V.vulnificus)6种海洋致病性弧菌的主要外膜蛋白, SDS-PAGE图谱比较发现这6种弧菌都存在36 kDa的外膜蛋白条带.通过电泳洗脱分离纯化这6种弧菌的36 kDa外膜蛋白,并制备了鳗弧菌菌株SJ060621的36 kDa外膜蛋白多抗.ELISA和Western-blot印迹结果显示,仅鳗弧菌SJ060621、S010610-1和哈维氏弧菌的36 kDa外膜蛋白存在免疫交叉反应;双向电泳分析了鳗弧菌SJ060621、S010610-1、哈维氏弧菌和溶藻弧菌的36 kDa外膜蛋白,2-DE图谱显示出鳗弧菌SJ060621和S010610-1均由3种等电点相近的蛋白组成,存在很高的同源性,2株鳗弧菌与溶藻弧菌和哈维氏弧菌在蛋白质组成数量和等电点上都存在较大的差异,结果说明通过主要外膜蛋白的分子量和免疫特性研究,可为筛选不同弧菌共同外膜蛋白的亚单位疫苗提供有利参考.  相似文献   

赤魟软骨血管生成抑制因子的分离纯化   总被引：2，自引：0，他引：2       下载免费PDF全文

余新威  钱晓  王婕妤  罗红宇  吴常文 《海洋学报》2008,30(1):113-118

确定了制备高纯度赤魟软骨血管生成抑制因子的纯化工艺,并通过胶原酶模型、CAM模型验证其生物学活性。正交实验确定了赤魟软骨组织抽提的最佳条件,抽提产率可达0.84%。丙酮分级沉淀对抽提产物进行粗分离,25~35%的丙酮分级产物的CAM血管生成抑制率达85%。优化离子交换层析、凝胶过滤、反相层析的条件,可进一步有效的获得高纯度的赤魟软骨血管生成抑制因子-I(DCAIF-I)。SDS-PAGE-考马斯亮蓝染色显示为一条带,分子量为62 kDa。活性验证结果表明,DCAIF-I对胶原酶具有一定的抑制活性,抑制率为36.3%,对CAM血管生成的抑制活性具有一定的剂量依赖关系。  相似文献