斑纹鲟凝集素(CFL)的初步研究Ⅱ.CFL的分子组成及性质鉴定

采用生化方法对斑纹鲟(Charybdis feriatus)凝集素进行了初步研究.结果表明,斑纹鲟的血清中有动物红细胞和微生物细胞凝集活性的凝集素(Charybdis feriatuslectin,CFL),其活力表现依赖于Ca2+,并为多种糖所抑制;CFL对40℃以上的温度敏感,其活力在pH6.0~8.0内稳定.经巯基乙醇处理和未经巯基乙醇处理的CFL在SDS-PAGE上均为一条蛋白带,说明斑纹鲟凝集素不含二硫键,且只有一种亚基,分子量为40.8 kDa,CFL氨基酸组成分析表明其富含酸性氨基酸.     

两种微藻凝集素对几种不同类型细胞的凝集作用

经离子交换和分子筛层析从紫球藻（Porphyridium cruentum）和海水小球藻（Chlorella sp．）中分离纯化得到2种凝集素,研究它们对几种不同类型细胞即动物和人血红细胞、海洋和淡水微藻、细菌和真菌的凝集活性。研究结果表明,2种微藻凝集素对它们当中一些类型的细胞或种类具有不同程度的凝集活性,其中对水生聚胞藻（Synechocystis aquetilis）的凝集活性最强,最低质量浓度只需0．0313g／L。     

草鱼血清中一种新的凝集素免疫因子

于1998年5月－2000年3月，在浙江省杭州市采集草鱼，采用硫酸铵盐析和梯度聚丙烯酰胺凝胶电泳技术，从血清中分离出一种自然凝集素，对其理化和生物学性质进行研究。结果表明，该凝集素能够识别和凝集多种不同的红细胞、细菌和酵母，具有100000g离心不沉降，不被透析，耐热、耐酸、耐碱，抗DNase、RNase、SDS和乙醚，对胰蛋白酶、糖苷酶、糖氧化剂NaIO4和β－巯基乙醇敏感等特性，是一种分子量为67kD、等电点为6．2的糖蛋白分子。其活性能被半乳糖、乳糖、甘露糖和N－乙酰葡糖胺所抑制，其抗原特异性不同于草鱼凝集集抗IgM，表明两者是不同的物质。草鱼凝集素显著地促进巨噬细胞的吞噬、杀菌能力，说明是一种重要的免疫活性因子。     

经酶修饰和未经酶修饰的鹌鹑红细胞对甲壳动物血清凝集素凝集活性的差异研究

为寻找凝集素作为分子探针提供基础资料,用12种甲壳动物血清抽提液对天然的或经酶修饰的鹌鹑红细胞进行凝集试验。实验结果表明,经蜗牛酶修饰后的鹌鹑红细胞的凝集作用发生了变化,与未经酶处理的鹌鹑红细胞相比,凝集活性提高的有日本沼虾（Macrobrachium nipponense）等7种,凝集活性下降的有罗氏沼虾（Macrobrachium rosenbergi）等2种。凝集素对动物红细胞的凝集可看作是与这些细胞表面的多糖或糖蛋白——即受体的识别性鲒合,这表明鹌鹑红细胞表面具有12种凝集素的受体,且大多数受体都受到酶修饰的影响,从而在凝集活性上表现出差异。     

磷沙蚕凝集素的分离纯化及生物活性研究

采用DEAE-Toyopearl阴离子交换树脂、Bio-Gel P-100分子筛层析、Lactosyl-Sepharose4B亲和层析和Sephadex 75分子筛层析技术从日本海的海洋无脊椎动物磷沙蚕(Chaetopterus variopedatus)中分离出2种凝集素,通过体外细胞活性和酶活性实验观察它们的生物活性。结果表明,从海洋无脊椎动物磷沙蚕中分离出一种β-半乳糖特异性凝集素(CVL)和一种具有血凝活性,但不被经测试的单糖和糖蛋白所抑制的相对分子质量为30 000的蛋白质(CVL-1)。β-半乳糖特异性凝集素(CVL)具有体外抑制NB4白血病细胞株的活性和抑制小鼠脾细胞的活性,IC50分别为7.87 mg/L和22 mg/L。同时,另一种蛋白质(CVL-1)具有β-葡萄糖苷酶活性。     

河流弧菌(Vibrio fluvialis)感染后牙鲆(Paralichthys olivaceus)血清抗菌物质的研究

采用1×107cells/ml的河流弧菌悬液背部肌肉注射感染牙鲆,注射后24h、48h试验组的血清抗菌活力分别极显著性(P0.01)和显著性(P0.05)高于对照组。用Sephadex G-25凝胶柱对第二次人工注射感染后24h牙鲆血清进行分离,其中第7—15收集管对河流弧菌具有抗菌活性,对大肠杆菌、枯草芽孢杆菌等指示菌也具有明显的抗菌作用,在4—100℃范围内,大部分活性分离组分随着温度的升高其抗菌活力有所增强。具有抗河流弧菌活性收集管(第9管)经弱阳离子交换柱分离后,OD280显示出2个蛋白吸收峰,具有抗河流弧菌活性的物质主要集中在第1吸收峰。SDS-PAGE分析显示经Sephadex G-25凝胶柱和弱阳离子交换柱分离的抗菌蛋白分子量较大。以上结果表明,牙鲆被河流弧菌感染后能很快产生大量抗菌物质释放到血清中;主要抗菌物质的分子量较大,且热稳定性较好;这些活性物质的抗菌活性具有较强的特异性。     

毛蚶血清凝集素的凝集活性

以毛蚶为实验材料,对其血清中的凝集素进行研究.毛蚶血清凝集素对人的A,B,O血型红细胞、鸡和小鼠的红细胞均有凝集作用,凝集效价分别为256,256,8,16,64,同时它还能对白色念珠菌、啤酒酵母、溶藻胶弧菌等微生物具有凝集作用.毛蚶血清凝集素具有一定的pH值稳定性和热稳定性.在选用的12种单糖和寡糖中,L-鼠李糖、L-树胶醛糖、麦芽糖、D-半乳糖、蔗糖对毛蚶血清的凝集活性有明显的抑制作用.用弧菌对毛蚶进行免疫刺激时,其血清对鸡红细胞的凝集效价明显增加.     

绒螯蟹凝集素的红细胞凝集活性分析

利用血凝试验及糖抑制试验测定一种绒螯蟹的血清及肌肉提取液的凝血活性及糖抑制专一性,同时进行热稳定性、pH及Ca^2 影响试验。结果显示：血清只能凝集9种红细胞,肌肉提取液能凝集12种红细胞。血清对鹌鹁红细胞的凝集可被乳糖、D-甘露糖、D-果糖、D-半乳糖4种糖所抑制,最小抑制浓度均为200mmol／L,其凝集活性均依赖于Ca^2 ,在pH为6．0～7.0范围内较稳定,经50℃保温10min后活性完全消失。肌肉提取液只被D-甘露糖抑制,在pH为4．0～10．0、温度为4℃～90℃范围内均具活性,说明有很强的耐热性,其凝集活性不依赖于Ca。以上结果表明：血清与肌肉提取液均含有凝集素,且凝集素的种类不同。     

利用鱼抗血清及鼠抗血清分析鱼肠道弧菌全菌蛋白抗原性

从患腹水症牙鲆脾脏组织中分离得到一株优势菌株CD86,经人工感染实验证实菌株CD86对牙鲆有较高的致病力,其半致死浓度为1.8×105 CFU/尾。通过生理生化特征测定和16SrDNA基因序列分析,判定菌株CD86为鱼肠道弧菌(Vibrio ichthyoenteri)。以福尔马林灭活的菌株CD86全菌分别免疫健康的小鼠和牙鲆,ELISA测定鼠抗血清和牙鲆抗血清效价分别为12 800和1 200。利用间接免疫荧光技术检测2种抗血清与菌株CD86的结合活性,结果显示,2种血清均可同菌体发生阳性反应,其中鼠抗血清阳性反应信号明显强于鱼抗血清。同时,利用Western blotting分析了菌株CD86全菌蛋白的抗原性,结果显示分子量为27、30和37kDa的菌体蛋白条带与2种血清均发生阳性反应;分子量为19、25、28、29和35kDa的菌体蛋白条带仅与鼠抗血清发生阳性反应;分子量为45kDa的菌体蛋白条带只与鱼抗血清发生阳性反应。研究结果表明,牙鲆对菌体抗原产生的抗体应答与小鼠存在明显差异,该发现对研筛鱼用高效的鱼肠道弧菌亚单位疫苗具有重要的参考价值。     

甲壳纲动物凝集素的结构特征和分离纯化方法

凝集素(Lectin)是指所有非免疫原的能凝集细胞或沉淀含糖大分子的蛋白质或糖蛋白,一般具有糖结合专一性,能与糖蛋白或糖脂分子中的糖相结合。早在1888年,俄国的Herman发现蓖麻籽的蛋白质提取物能凝集血红细胞,从而开始了凝集素的研究。目前人们分离纯化的凝集素已经超过了1 000     

Target-directed isolation and identification of a serum lectin from lamprey (Lampetra japonica) by chromatographys and MALDI-TOF/TOF

A 105-k Da polymer lectin was purified from lamprey(Lampetra japonica) serum by chromatography methods including cation ion-exchange chromatography with a SP-Sepharose TM XL column and size exclusion chromatography with a Superdex 200 column. The target fractions were collected according to the direction of hemagglutinating activity. The results revealed that the active fractions could adsorb on SP-Sepharose column and showed a 280 nm UV absorbance peak corresponding to molecular weights of 105 k Da in the following size exclusion chromatography. The target fractions with hemagglutinating activity were further checked by NativePAGE and SDS-PAGE. Two single bands at around 105 k Da and 35 k Da were displayed by two electrophoresis methods respectively, indicating that the protein exists as a trimer in solution. After Native-PAGE and SDS-PAGE,two bands were excised from the gels respectively and further identified by MALDI-TOF/TOF as serum lectin(gi:13094239). The lectin was able to agglutinate rabbit red blood cells(RRBCs) and sheep red blood cells(SRBCs) in vitro. The lectin isolated from lamprey serum in the current study might be helpful for deeply understanding the innate immune molecules dependent immune defence in jawless vertebrates which have been proved recently that they possess a lymphocyte-based system of anticipatory immunity with variable lymphocyte receptors as mediators.     

瓦氏黄颡鱼(Pelteobagrus vachelli)卵黄蛋白原的纯化、性质鉴定及ELISA检测方法的建立

腹腔注射17β-雌二醇(E2),使瓦氏黄颡鱼雄鱼在7天内产生卵黄蛋白原(Vtg)。采用凝胶过滤和离子交换两种层析技术,从E2诱导的雄性瓦氏黄颡鱼血浆中分离、纯化出Vtg,采用糖、磷、脂蛋白染色技术证明分离、纯化的蛋白为Vtg,该Vtg在非变性条件下分子量约为240kDa,在SDS变性条件下分子量约为143kDa。纯化的瓦氏黄颡鱼Vtg经检测显示可能含有类胡萝卜素,但没有二硫键,对热相对稳定。利用纯化的瓦氏黄颡鱼Vtg,制备了兔抗瓦氏黄颡鱼Vtg多克隆抗血清。用双向免疫扩散法测得抗血清的纯度较高,效价为1︰32;Western blotting检测显示抗血清的特异性较好。以瓦氏黄颡鱼Vtg多克隆抗血清为抗体,以纯化的瓦氏黄颡鱼Vtg为抗原,建立了间接酶联免疫吸附反应(ELISA)方法检测瓦氏黄颡鱼体内Vtg的含量,标准曲线线性部分的线性方程为y=0.099x+0.4529(R2=0.9327),该方法检测的灵敏度为15.6ng/ml,工作范围为31.2—4000ng/ml,在此范围内,标准曲线具有良好的线性。     

鲨鱼和魟鱼肝铁蛋白电泳纯的制备技术

采用硫酸铵分级盐析、DEAE阴离子交换层析、Sephacryl S—300凝胶层析技术分离纯化鲨鱼肝铁蛋白(Liver ferritin of Sphyma zygaena,SZLF)和虹鱼肝铁蛋白(Liver ferritin of Dasyatis akajei,DALF)。电子显微镜技术揭示了SZLF和DALF的分子结构,阐明了两者蛋白均由蛋白壳和铁核组成。柱层析和电泳技术拓展了电泳纯的SZLF和DALF制备方法,并可用于制备其他高纯度的铁蛋白。     

病毒膜蛋白及其表达和纯化技术的研究进展

病毒囊膜是包膜病毒除核衣壳外的另一主要成分。它主要由多种蛋白质构成，称为膜蛋白，膜蛋白以单聚体，二聚体，三聚体，甚至更多的聚合体的形式存在，具有中和抗体，与靶细胞受体结合，凝集红细胞，诱导细胞融合等多种功能，膜蛋白可采用将其基因整合入载体，并在昆虫细胞，哺乳细胞或细菌中获得体外表达，膜蛋白可在去污剂的作用下形成蛋白质－脂－去污剂的复合物而被溶解，其中去污剂的临界微团浓度，亲水物－亲脂物平衡值，荷电、紫外穿透性等是选择合适去污剂的主要参考因子，溶解后的膜蛋白多利用聚丙烯酰胺凝胶电泳、凝胶过滤层析，离子交换层析，亲和层析，高效液相层析等技术并结合梯度离心；分级沉淀等进行分离、纯化。     

Similarity of electrophoretic dissolved protein spectra from coastal to pelagic seawaters

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.     

近海温泉中嗜热菌Geobacillus sp. ZH1锰超氧化物歧化酶的克隆与表达

将嗜热菌Geobacillus sp. ZH1的超氧化物歧化酶(supseroxide dismutase,SOD)基因插入表达载体pET-32α(+),在Escherichia coli BL21(DE3)中进行表达,并利用亲和层析纯化重组超氧化物歧化酶.将制备的脱辅SOD进行Mn2+和Fe2+金属重构后,得到的Mn2+重构SOD的比活力达668U/mg,Fe2+重构Fe-SOD没有活性,说明ZH1菌株的超氧化物歧化酶为Mn-SOD.凝胶过滤及SDS-PAGE分析显示,Mn2+重构SOD为同聚二聚体,亚基分子量为71.7 kDa.这些研究结果为进一步研究该酶的生化特性及酶的定向进化研究奠定了良好的基础.     

Development of two novel CYP-antibodies and their use in a PCB exposure experiment with Mytilus edulis

In an attempt to learn more about the cytochrome P450 (CYP) system of mussels, we used protein databases and alignment software to extract highly conserved CYP sequences. From these alignments synthetic peptides were produced and used for rabbit immunisation, which yielded polyclonal antibodies against the CYP families 2 and 4. The antibodies were evaluated with Western Blot and ELISA assays, using digestive gland microsomal samples from the mussel Mytilus edulis. Western Blots revealed immunoreactions for both antibodies. The anti-CYP2 sequence rendered one major immunopositive protein of ≈49 kDa size, and weak signals for proteins of ≈41 and 56 kDa size. The anti-CYP4 sequence rendered two major bands of ≈56 and 59 kDa size, and also a weak immunoreaction with a protein of ≈43 kDa size. ELISA rendered only weak signals even with a 1:50 dilution of IgG-purified serum. A 10-day exposure to Aroclor 1254 did not appear to affect any of the immunopositive proteins, while total PCBs in soft bodies increased from 14–40 ng/g DW in controls to 373–638 ng/g DW in exposed mussels.     

海洋真菌Neosartorya fischeri 1008F1的次级代谢产物抑菌及抗肿瘤活性的研究

通过抑菌及抗肿瘤活性实验,明确海洋真菌Neosartorya fischeri 1008F1次级代谢产物中的活性有效组分。应用对峙培养法和生长速率法,对菌株的抑菌活性进行测定。应用MTT法,对菌株的抗肿瘤活性进行测定。应用凝胶(Sephadex LH-20)柱层析的方法,对菌株发酵产物的提取物进行分离。结果发现,海洋真菌Neosartorya fischeri 1008F1的水溶性提取物对番茄早疫菌(Alternaria solani)具有一定的抑制活性。菌株的粗提物浸膏经Sephadex LH-20柱梯度洗脱后,得到的组分B、C、D、E和F。在0.5 g/L的供试浓度下,组分B、C和D对胃癌细胞SGC-7901的抑制率均高于80%,而组分B、C、D、E和F对肝癌细胞BEL-7404的抑制率均高于70%。     

Advanced characterization of marine dissolved organic matter by combining reversed-phase liquid chromatography and FT-ICR-MS

Marine dissolved organic matter (DOM) was separated by reversed-phase (RP) liquid chromatography method and analyzed with fluorescence/absorption detection and Fourier transform ion cyclotron mass spectrometry (FT-ICR-MS). The three key characteristics of the RP method are: (a) The C18-RP column chosen provides enhanced separation when the aqueous phase is 100% buffer-free water, and it does not degrade over time; (b) the water eluent adjusted to pH 7 significantly improves the resolution of water soluble compounds; (c) the initial flow maintained at low levels improves the separation of polar compounds. In samples, containing “fresh” DOM, specific peaks were detected, which were absent in “old” DOM samples. The combination with size exclusion chromatography (SEC) also demonstrated the relation between polarity and molecular size of DOM. FT-ICR-MS was applied to evaluate the quality of separation on a molecular scale demonstrating that physico-chemical characteristics of DOM can be related to molecular formulas. Sample extracts were separated into 4 preparative fractions, and a large suite of the identified molecular formulas only occurred in specific fractions. This is an important basis for the application of further analytical techniques in order to perform a more target-oriented analysis aiming at the determination of source and process biomarkers for DOM.     

4 种病原弧菌外膜蛋白的提取及抗原性初步分析

利用十二烷基磺酸钠抽提并结合超速离心的方法提取了鳗弧菌(Vibrio anguillarum)、河口弧菌(V.aestuarianus)、霍乱弧菌(V.cholerae)和副溶血弧菌(V.parahaemolyticus)4种致病性弧菌的主要外膜蛋白,通过SDS-PAGE分析比较4种弧菌主要外膜蛋白的组分。结果表明:4株弧菌的外膜蛋白电泳图谱一般可得到5～10条蛋白带,分子量多数集中在26~40 kD和48~85 kD。对所提取的4种弧菌主要外膜蛋白进行SDS-PAGE后,分别与自制的兔抗鳗弧菌血清、抗河口弧菌血清、抗副溶血弧菌血清进行Western-blotting印迹分析。结果显示每种全菌抗血清可与相应菌的外膜蛋白部分组分发生免疫反应,并与其他3种弧菌外膜蛋白的部分组分产生交叉免疫反应,这些反应条带分子量主要集中于30~48 kD之间。本研究为进一步研究致病性弧菌外膜蛋白免疫学特性提供参考。